Rare Diseases ISS
Rare Diseases ISS
Rare Diseases ISS
ABSTRACT BOOK
Edited by
Domenica Taruscio and Marco Salvatore
Centro Nazionale Malattie Rare
ISSN 0393-5620
ISTISAN Congressi
08/C10
Istituto Superiore di Sanità
Workshop. Projects on rare diseases funded within the bilateral agreement Italy (Istituto
Superiore di Sanità) and USA (NIH, Office for Rare Diseases) on joint research and development
of public health actions. Istituto Superiore di Sanità. Rome, October 29-31, 2008. Abstract book.
Edited by Domenica Taruscio and Marco Salvatore
2008, xvii, 154 p. ISTISAN Congressi 08/C10
The International Conference on rare diseases and orfan drugs (October, 27th-31st, 2008) is an annual
meeting aimed to illustrate Italian and European activities as well as the new developments concerning
rare diseases and orphan drugs. The first two days of the meeting (27 and 28 October) will be dedicated
to the presentation and discussion of the main European and Italian activities on rare disease and orphan
drugs; from the 29 to the 31 of October, during the second workshop entitled "Projects on rare diseases
funded within the bilateral agreement Italy (Istituto Superiore di Sanità) and USA (NIH, Office for Rare
Diseases) on joint research and development of public health actions", the results of the research
projects, funded within the bilateral agreement (Italy-USA) on joint research and development of public
health actions between ISS and NIH-Office for Rare Diseases will be presented. In this abstract book, we
collected all the scientific contributions from the scientific responsible of each project funded.
Key words: Rare diseases, Orphan drugs, Research
La Conferenza Internazionale sulle malattie rare ed i farmaci orfani (27-31 ottobre, 2008)
rappresenta un appuntamento annuale durante il quale vengono illustrate le attività intraprese a livello
naizonale nel settore malattie rare e farmaci orfani e proposte possibili nuove iniziative tenendo conto
anche del più ampio contesto europeo. Nei primi due giorni della Conferenza (27-28 ottobre) ampio
spazio sarà dedicato alla presentazione ed alla discussione delle principali novità europee ed italiane
sulle iniziative ed attività nel campo delle malattie rare e farmaci orfani. Negli ultimi tre giorni della
Conferenza (29-31 ottobre) si svolgerà il secondo workshop finalizzato a presentare i risultati
raggiunti nell'ambito dei progetti finanziati nel contesto dell'accordo bilaterale Italia-USA (ISS/NIH-
Office for Rare Diseases). Nel presente volume sono stati raccolti tutti gli abstract elaborati da
ciascun Responsabile di progetto e presentati nel corso del workshop.
Parole Chiave: Malattie rare, Farmaci orfani, Ricerca
i
ii
PROGRAMME
Session I
ASPECTS OF PATHOGENESIS
Chairpersons: Stephen Groft, Domenica Taruscio
iii
10.30 Transcriptional study of p63alpha mutants found
in ectodermal dysplasia syndromes
Eleonora Candi, Rita Cipollone, Andrea Codispoti, Gerry Melino,
Alessandro Terrinoni
10.45 Discussion
Session II
ASPECTS OF PATHOGENESIS
Chairpersons: Filippo Belardelli, Tamara C. Petrucci
iv
12.50 Neurological impairment in Niemann-Pick C disease: a study on the role
of excitatory neurotrasmitter receptors and identification
of peripheral cellular biomarkers
Claudio Frank, Daniele Grossi, Giovanna De Chiara, Mauro Racaniello,
Giuseppe Biagini, Virginia Tancredi, Stefano Rufini, Daniela Merlo,
Giovanna D'Arcangelo
13.05 Discussion
Session III
ASPECTS OF PATHOGENESIS
Chairpersons: Douglas Noonan, Giuseppe Novelli
v
15.45 Tackling rare diseases yet lacking diagnosis and/or prognosis: a pilot project
integrating data collection and experimental studies
Domenica Taruscio, Antonio Antoccia, Gianluca Azzalin, Rita Devito,
Alessandra Di Masi, Stefano Lorenzetti, Giuseppe Macino,
Armando Magrelli, Alberto Mantovani, Francesca Maranghi,
Gabriele Moracci, Sara Nicolai, Caterina Tanzarella,
Marco Salvatore, Roberta Tassinari, Fabrizio Tosto, Mara Viganotti
16.00 Discussion
Session IV
ASPECTS OF PATHOGENESIS
Chairpersons: Giuseppe Novelli, Giandomenico Russo
16.30 SOX7 and -17 function as modifiers of the lymphangiogenic role of SOX18.
New insights in the pathogenesis of the human syndrome hypotrichosis-
lymphedema-telangiectasia
Brett Hosking, Mathias François, Andrea Caprini, Fabrizio Orsenigo,
Francesco Bertolini, Elisabetta Dejana, Peter Koopman
vi
Thuersday, October 30, 2008
Session I
DIAGNOSIS
Chairpersons: Bruno Dallapiccola, Maurizio Pocchiari
9.00 Genomic diagnosis and classification of rare disorders with mental retardation
using high throughput technologies
Laura Bernardini, Antonio Novelli, Bruno Dallapiccola
9.45 Molecular analysis of ARSA and psap genes in twenty-one Italian patients
with metachromatic leukodystrophy. Identification and functional characterization
of 11 novel ARSA alleles
Serena Grossi, Stefano Regis, Camillo Rosano, Alessandra Biffi,
Fabio Corsolini, Maria Sessa, Mirella Filocamo
10.00 A genome wide non-synonymous snp scan of Amyotrophic Lateral Sclerosis (ALS)
Isabella Fogh, Antonia Ratti, Cinzia Gellera, Ferdinando Squittieri,
John Powell, Vincenzo Silani
10.45 Discussion
vii
Session II
DIAGNOSIS
Chairpersons: Eloisa Arbustini, Walter Malorni
viii
12.45 Systematic diagnosis of rare erythroenzymopathies: generation of guidelines
and study of the genotype/phenotype correlation
Wilma Barcellini, Paola Bianchi, Elisa Fermo, Giovanna Valentini,
Alberto Zanella
13.00 Discussion
Session III
DIAGNOSIS
Chairpersons: Lidia Larizza, Giampaolo Merlini
15.00 Family based transmission analysis of genetic markers in class I and class III HLA
region in Sardinian children with autistic spectrum disorders
Franca R. Guerini, Elisabetta Bolognesi, Sonia Usai,
Salvatorica Manca, Mario Clerici
ix
Pierluigi Granone, Mauro Antimi, Maurizio Lalle, Anna Ceribelli,
Massimo Rinaldi, Giuseppina Chichierchia, Salvatore Conti, Enzo Gallo,
Gerardina Merola, Raffaele Perrone Donnorso, Mauro Piantelli
16.15 Discussion
Session IV
DIAGNOSIS
Chairpersons: Lidia Larizza, Giovanna Zambruno
17.00 Biochemical and cellular real-time biomarkers of diagnostic and prognostic value
in the management of Kawasaki's disease
Donatella Pietraforte, Elisabetta Straface, Alessio Metere,
Lucrezia Gambardella, Luciana Giordani, Elisabetta Cortis, Alberto Villani,
Domenico Del Principe, Marina Viora, Maurizio Minetti, Walter Malorni
x
17.45 Development of an epidemiological and molecular integrated approach
for the prevention of congenital hypothyroidism: preliminary results
Roberto Cerone, Mario De Felice, Roberto Di Lauro,
Emanuela Medda, Luca Persani, Domenica Taruscio,
Massimo Tonacchera, Antonella Olivieri
Session I
TREATMENT AND CLINICAL MANAGEMENT
Chairpersons: Adriana Albini, Stefano Vella
xi
10.00 Targeting the prognostic and metastasis-predicting surface proteoglycan
for immunotherapeutic treatment of selected sarcomas
Roberto Perris, Sabrina Cattaruzza, Pier Andrea Nicolosi,
Maria Teresa Mucignat, Katia Lacrima, Nicoletta Bertani,
Laura Pazzaglia, Maria Serena Benassi, Lucia Sigalotti,
M. Guidoboni, Michele Maio, W.B. Stallcup, Piero Picci
10.30 Therapy-oriented large scale genomic and gene expression analysis in thymomas,
mesotheliomas and lung carcinoids
Francesca Toffalorio, Elena Belloni, Caterina Fumagalli, Soheil Javan,
Carla Micucci, Simone Paolo Minardi, Myriam Alcalay, Giuliana Pelicci,
Giuseppe Pelosi, Lorenzo Spaggiari, Filippo de Braud, Tommaso De Pas
10.45 Discussion
Session II
TREATMENT AND CLINICAL MANAGEMENT
Chairpersons: Ruggero De Maria Marchiano, Alfredo Gorio
11.30 Mesenchymal stem cells for the treatment of tibial congenital pseudarthrosis
associated with type I neurofibromatosis
Donatella Granchi, Valentina DeVescovi, Elisa Leonardi, Serena R. Baglio,
Onofrio Donzelli, Marina Magnani, Armando Giunti, Nicola Baldini
11.45 Adipose tissue-derived stem cells for the treatment of muscular dystrophy
Ilaria Gatto, Antonietta Gentile, Gabriele Toietta,
Maurizio C. Capogrossi, Giuliana Di Rocco
xii
12.00 Experimental cell therapy in osteopetrosis
Alfredo Cappariello, Anna C. Berardi, Barbara Peruzzi, Andrea Del Fattore,
Alberto Ugazio, Gian Franco Bottazzo, Anna Teti
12.15 Therapeutic potential of stem cell factor in the human beta-thalassemia treatment:
in vitro and in vivo studies
Ann Zeuner, Monica Bartucci, Ornella Morsilli, Nadia Maria Sposi,
Marta Baiocchi, Paolo Cianciulli, Ruggero De Maria, Marco Gabbianelli
13.00 Discussion
Session III
TREATMENT AND CLINICAL MANAGEMENT
Chairpersons: Stefano Fais, Giandomenico Russo
xiii
15.15 Quality of life and disability in Fabry disease
Costanza Pazzaglia, Pietro Caliandro, Matteo Russo, Andrea Frustaci,
Claudio Feliciani, Luca Padua
16.15 Discussion
Session IV
TREATMENT AND CLINICAL MANAGEMENT
Chairpersons: Bruno Bembi, Angelo Selicorni
16.45 New findings from MECP2-308 and KFL7 mice as models of mental retardation
Giovanni Laviola, Laura Ricceri, Bianca De Filippis, Carla Perrone-Capano,
Maria Giuseppina Miano
xiv
17.15 Enzyme replacement therapy with alglucosidase alfa in juvenile-adult
glycogenosis type 2 patients
Bruno Bembi, Sabrina Ravaglia, Federica Edith Pisa, Giovanni Ciana,
Agata Fiumara, Marco Confalonieri, Rossella Parini, Miriam Rigoldi,
Arrigo Moglia, Alfredo Costa, Cesare Danesino, Andrea Dardis
18.00 Testing in vitro and in vivo treatments for inclusion body myositis
Simona Saredi, Claudia Di Blasi, Pia Bernasconi, Lucia Morandi,
Renato Mantegazza, Marina Mora, Cristina Sancricca, Enzo Ricci,
Pietro Attilio Tonali, Massimiliano Mirabella
xv
xvi
NOTES FOR READERS
This abstract book presents the oral and poster presentations illustrated during the three
days Workshop (29th-31st, October, 2008) organized in the frame of the annual international
Conference on rare diseases and orphan drugs (Istituto Superiore di Sanità, 27th-31st October,
2008). The abstracts are listed in alphabetical order based on the first author of the
contribution. Posters are indicated by the letter "P" before the title. All authors of the abstracts
are listed at the end of the volume, in the specific "author index".
The programme of the Workshop is included; all abstracts are presented as oral or poster
presentations.
xvii
xviii
Communications and Posters
1
2
ANGIOGENESIS AND INFLAMMATION AS TARGET
FOR RETINOBLASTOMA THERAPY
Adriana Albini (a), Rosaria Cammarota (a), Roberta Venè (b), Gianfranco Fassina (b),
Massimo Nicolò (c), Douglas M. Noonan (d), Francesca Tosetti (b)
(a) IRCCS Multimedica, Milano
(b) Laboratorio di Oncologia Molecolare, Istituto Nazionale per la Ricerca sul Cancro,
IST, Genova
(c) Dipartimento di Neuroscienze, Genetica e Oftalmologia, Sezione Clinica Oculistica,
Università degli Studi, Genova
(d) Dipartimento di Scienze Cliniche e Biologiche, Università degli Studi dell'Insubria,
Varese
Introduction. Ocular tumors, in particular retinoblastoma and uveal melanoma, are rare
diseases but with a very high impact on patients. The conventional chemotherapy is toxic
so our aim was to identify new molecular targets to restrain tumour progression without
damages for patients. Both are highly vascular and appear to be readily targeted by anti -
angiogenic agents.
Methods. The sensitivity of Y79 cells to different prooxidant anticancer drugs
including the synthetic retinoid N-(4-hydroxyphenyl)retinamide (4HPR), arsenic trioxide
(As2O3) and phenetyl isothiocyanate (PEITC) was assessed by the MTT assay, ATP content
quantification and release of extracellular lactate dehydrogenase Survival signaling
stimulated by the Insulin-like Growth Factor I (IGF-I) and cell death pathways were
analyzed in prooxidant-treated cells in vitro and correlated with proangiogenic IGF-1
signaling in the matrigel sponge model assay in vivo. To further examine the potential of
targeting the microenvironment as a strategy to control tumor growth, we adopted a gene
transduction approach using a potent TH1 cytokine endowed with strong anti-angiogenic
activity, Interleukin-12 (IL-12). Gene transfer into murine 99E1 ocular tumor cells, while
having no effects on growth in vitro, essentially blocked growth of vascular tumors in vivo
without evident signs of toxicity. The 99E1 cell line was derived from a choroidal/retinal
pigmented epithelial ocular tumor that arose in a transgenic FVB/N mouse bearing the
SV40 oncogene.
Results. In Y79 cells treated with 4HPR where IGF-I-induced AKT phosphorylation
was repressed, phosphorylation at Ser 9 of the multifunctional kinase glycogen synthase
kinase 3β (GSK3β) was sustained. All the prooxidant drugs investigated were able to
induce GSK3β phosphorylation, which was reversed by chemically different antioxidants,
concomitant with mitochondrial and nuclear apoptosis and ATP depletion. The in vivo
angiogenesis assay revealed that IGF-1 receptor stimulation remarkably contributes to the
proangiogenic potential of retinoblastoma cells. Orthotopic intraocular injection resulted in
invasive tumors that destroyed ocular architecture by the control cells while the IL-12
transduced cells rarely formed tumors. Histological analysis revealed highly invasive and
angiogenic tumor growth in the controls and poorly vascularized tumors in the presence of
IL-12. The tumor repression effect could be reproduced by a systemic anti-angiogenic
effect, where controlateral injection of IL-12 expressing cells strongly repressed growth in
3
tumors formed by parental 99E1 cells. This was associated with significantly lowered
tumor vessel densities, a trend towards lower VEGF levels in the lesion, and significantly
decreased NK cells in the parental tumors exposed to systemic IL-12.
Conclusions. Prooxidant anticancer drugs interfere with retinoblastoma survival and
proangiogenic signaling pathways thus suggesting potential application at clinical level. IL-
12 gene transfer can provide anti-angiogenic effects without toxicity and may be
particularly suited for therapy of vascularized ocular tumors.
4
DEVELOPMENT OF NEW STRATEGTIES
OF MOUSE AMELANOMA VACCINATION USING
L19MTNFΑ AS AN ADJUVANT
The antitumor effects of the pro-inflammatory cytokine TNFα are mainly due to the
preferential toxicity for the tumor-associated vasculature and to the ability to potentiate the
immune response against tumors. For these reasons, TNFα could be used as an adjuvant in
the formulation of antitumor vaccines.
L19mTNFα is a fusion protein composed by the scFv L19, specific for the highly
conserved ED-B domain of fibronectin, a tumor-associated antigen identical in humans and
mice, and m(ouse)TNFα that, in different mouse tumor models, induces a therapeutic T
cell-mediated immune response that protects the host against syngeneic tumors of different
histological origin.
The purpose of this study was to evaluate the efficacy of L19mTNFα as an adjuvant in
vaccination protocols with melanoma homogenates.
Two melanoma models (B16F1 and B16BL6B17) were established in the syngeneic
C57 black mice. These melanomas are low immunogenic tumors that grow fast and do not
respond to the systemic therapy with L19mTNFα and melphalan that, on the contrary,
cures 80% of WEHI-164 fibrosarcoma- and 20-30% of C51 colon carcinoma-bearing mice.
Mice were s.c. injected at 3 week intervals with melanoma homogenate (80 mg/mouse)
with or without the addition of L19mTNFα (1 μg/mouse). Three weeks after the last
vaccination, a tumorigenic dose of melanoma cells was s.c. inoculated and the tumor
growth was recorded.
Up to three injections of tumor homogenate, supplemented or not with L19mTNFα,
determined no significant B16F1 or B16BL6B17 tumor growth delay in all the vaccinated
groups respect to controls. Moreover, the treatment with L19mTNFα and melphalan didn't
induce valuable therapeutic advantages in the vaccinated mice respect to controls. On the
contrary, after four injections, the mice vaccinated with tumor homogenate supplemented
with L19mTNFα developed palpable tumors one week after the controls and three days
after the mice vaccinated with homogenate only. Moreover, in the same group of animals
the therapy with L19mTNFα and melphalan determined a reduction in the tumor growth
rate that almost doubled the life-span expectancy. Noteworthy, after the third injection, all
the mice vaccinated with homogenate supplemented with L19mTNFα presented patches of
alopecia areata and hair depigmentation usually associated to autoimmunity and described
in mice actively immunized in the presence of adjuvants.
5
SYSTEMATIC DIAGNOSIS OF RARE
ERYTHROENZYMOPATHIES:
GENERATION OF GUIDELINES AND STUDY
OF THE GENOTYPE/PHENOTYPE CORRELATION
Wilma Barcellini (a), Paola Bianchi (a), Elisa Fermo (a), Giovanna Valentini (b,c), Alberto
Zanella (a)
(a) Divisione di Ematologia, Fondazione IRCCS, Ospedale Maggiore Policlinico
Mangiagalli e Regina Elena, Milano
(b) Dipartimento di Biochimica, Università degli Studi, Pavia
(c) Dipartimento di Genetica e Microbiologia, Università degli Studi, Pavia
6
consider normal reference intervals from a group of neonates because in some cases
enzymatic activity could be different from adults causing inappropriate diagnosis.
Subsequently, we will review all diagnostic pathways of hemolytic anemias, and a flow
chart will be created for each type of erythroenzymopathy, both considering diagnostic and
therapeutic aspects. This will permit to extend the knowledge on patho-physiological and
clinical aspects of RBC enzymopathies by a close cooperation of Experts and Expert
Centres and it will facilitate clinicians in rapid identification of red blood cell enzyme
defects and in appropriate treatment.
7
P. GENOTYPE/BEHAVIOURAL PHENOTYPE
CORRELATIONS IN CORNELIA DE LANGE SYNDROME
Emanuele Basile (a), Laura Villa (a), Lidia Larizza (b,c), Silvia Russo (c), Cristina
Gervasini (b), Paola Castronovo (b), Marta Cerutti (d), Anna Cereda (d), Alice Passarini (d),
Renato Borgatti (a), Angelo Selicorni (d)
(a) IRCCS Eugenio Medea, Associazione La Nostra Famiglia, Bosisio Parini, Lecco
(b) Scuola di Specializzazione in Genetica Medica, Azienda Ospedaliera San Paolo, Polo
Universitario, Milano
(c) Laboratorio di Citogenetica e Genetica Molecolare Umana, IRCCS Istituto Auxologico
Italiano, Milano
(d) I Clinica Pediatrica, Fondazione IRCCS, Ospedale Maggiore Policlinico Mangiagalli e
Regina Elena, Milano
8
Our preliminary results confirm the difficulty in establish clear correlation at individual
level between genotype and neuro-behavioural phenotype. Moreover the great majority of
CdLS patients with borderline mental development don't show any known genetic defect
while subjects with a diagnosis of autism show an high percentage of NIPBL mutations.
9
P. A REPRODUCTIVE RISK QUESTIONNAIRE
IN FAMILIES WITH A CHILD AFFECTED
BY CORNELIA DE LANGE SYNDROME
Maria Francesca Bedeschi (a), Vera Bianchi (a), Faustina Lalatta (a), Donatella Milani (b),
Francesca Menni (b), Silvia Maitz (b), Marta Cerutti (b), Angelo Selicorni (b)
(a) Unità Operativa Dipartimentale di Genetica Medica, Dipartimento Area Salute della
Donna, del Bambino e del Neonato, Fondazione IRCCS, Ospedale Maggiore
Policlinico Mangiagalli e Regina Elena, Milano
(b) Ambulatorio di Sindromologia, I Clinica Pediatrica, Fondazione IRCCS, Ospedale
Maggiore Policlinico Mangiagalli e Regina Elena, Milano
10
These results show a lack of knowledge about the genetic heterogeneity of the syndrome
by the families up to now evaluated the need of revaluation of the inheritance patterns and
risk estimation, applying the new knowledge about the aetiology of this disease.
11
TRAUMA AND RISK OF AMYOTROPHIC
LATERAL SCLEROSIS
There is no valuable evidence on the role of environmental risk factors in patients with
Amyotrophic Lateral Sclerosis (ALS). Traumatic events (single or repeated) have been
quite extensively investigated and several studies showed traumatic events being present to
a greater extent in the history of patients with ALS than in the general population. However
this evidence is still controversial because of methodological issues (recall bias, referral
patients, under-ascertainment of trauma). The aims of the study are: whether or not ALS
patients are at increased risk of trauma, repeated trauma, severe trauma; whether the site of
the major trauma coincides with the site of onset of symptoms; to verify the consistency of
the association in subgroups of patients from different geographic areas.
This population based case-control study includes three Italian regions (Lombardia,
Piemonte, Puglia) with population-based registries enrolling newly diagnosed residents
with ALS. Each patient diagnosed since January 1 2007 is matched for age, sex and
residency to two hospital controls (neurological and non neurological).
For each patient demographic and clinical data are collected. The diagnosis is made
according to the El Escorial criteria (original & revised). The consistency of the data is
tested in each regional registry separately and in multivariate analysis models adjusting for
the main confounders (professional activity, alcohol intake, smoking, exposure to
potentially toxic agents, family history of degenerative disorders).
Based on literature records, about 1% of individuals in the general population reports a
history of severe traumatic events. If ALS carries a 4-fold risk of traumatic events, a total of
410 patients and 819 controls must be recruited in 2 years (alpha 0.05; beta 0.8). The study
is also powered to detect a 5-fold risk of trauma by recruiting 244 ALS patients and 488
matched controls.
As of July 1 2008, a total of 105 patients (male 56.2%; mean age 66 years) and 91
matched controls were recruited. According to the revised El-Escorial criteria, 38 patients
had definite ALS, 20 had probable ALS and 6 had possible ALS (diagnostic category non
specified in 41 cases). 51 patients with ALS (48.6%) with data available reported a history
of at least one traumatic event (35 controls; 49.3%) (Odds Ratio 1.3, 95% CI 0.7-2.4).
12
GASTROESOPHAGEAL REFLUX
IN SYSTEMIC SCLEROSIS: RELATIONSHIP
WITH PULMONARY INVOLVEMENT
Laura Belloli (a), Roberta Barbera (b), Camilla Gambaro (b), Giacomo Rando (b), Nicoletta
Carlo-Stella (a), Bianca Marasini (a), Alberto Malesci (b)
(a) Unità di Reumatologia, IRCCS Istituto Clinico Humanitas, Università degli Studi,
Milano
(b) Dipartimento di Gastroenterologia ed Endoscopia, IRCCS Istituto Clinico Humanitas,
Università degli Studi, Milano
13
ENZYME REPLACEMENT THERAPY
WITH ALGLUCOSIDASE ALFA IN JUVENILE-ADULT
GLYCOGENOSIS TYPE 2 PATIENTS
Bruno Bembi (a), Sabrina Ravaglia (b), Federica Edith Pisa (c), Giovanni Ciana (d), Agata
Fiumara (e), Marco Confalonieri (f), Rossella Parini (g), Miriam Rigoldi (g), Arrigo Moglia (b),
Alfredo Costa (b), Cesare Danesino (h), Andrea Dardis (a)
(a) Centro Regionale per le Malattie Rare, Azienda Ospedaliera-Universitaria Santa Maria
della Misericordia, Udine
(b) Dipartimento di Neurologia, Fondazione Istituto Neurologico Casimiro Mondino,
IRCCS, Pavia
(c) Istituto di Igiene ed Epidemiologia, Azienda Ospedaliera-Universitaria Santa Maria
della Misericordia, Udine
(d) Struttura Complessa di Terapia Intensiva Neonatale, IRCCS Burlo Garofolo, Trieste
(e) Clinica Pediatrica, Università degli Studi, Catania
(f) Struttura Complessa di Pneumologia, Azienda Ospedaliero-Universitaria, Ospedali
Riuniti, Trieste
(g) Clinica Pediatrica, Università degli Studi, Monza
(h) Istituto di Genetica, Università degli Studi, Pavia
14
PRECLINICAL STUDIES AIMED TO DEVELOP TARGET
GENES-BASED THERAPIES FOR THE TREATMENT
OF AMYOTROPHIC LATERAL SCLEROSIS
Caterina Bendotti (a), Marco Peviani (a), Tiziana Borsello (a), Roberto Piva (b)
(a) Dipartimeno di Neuroscienze, Istituto di Ricerche Farmacologiche Mario Negri,
Milano
(b) Dipartimeno di Patologia e Centro di Medicina Sperimentale, CeRMS, Università degli
Studi, Torino
15
GENOMIC DIAGNOSIS AND CLASSIFICATION
OF RARE DISORDERS WITH MENTAL RETARDATION
USING HIGH THROUGHPUT TECHNOLOGIES
Copy Number Variations (CNVs) represent a major cause of Mental Retardation (MR),
especially when it is associated to Multiple Congenital Anomalies (MCA). In the last few
years, DNA microarrays have increased capabilities for detection of cryptic pathogenic
CNVs by analyzing the entire genome. Several commercially platforms, including a large
number of spotted sequences, oligonucleotides or Single-Nucleotide Polymorphisms
(SNPs), are now available to study the whole genome at a high resolution.
We have examined during last year 204 subjects with MR using an oligonucleotide-
array with an average resolution of 75 Kb, and disclosed 35 pathogenic CNVs in 33
patients (16%), spanning 0.208-22.473 Mb. These results confirmed the oligonucleotide
array-CGH to be a powerful tool in the study of MR. Forty MR/MCA patients, selected
from the original cohort of 204 subjects, were re-run on a commercial SNP-array platform,
consisting of about 250,000 SNPs with an average spacing of 10 Kb. Twenty eight resulted
negative with oligonucleotide-array analysis, while 12 were positive (30%). This analysis
allowed to compare the robustness and the cost/effectiveness of the two platforms in
detecting pathogenic cryptic genomic changes. SNP-array analysis detected 24 CNVs in 16
different patients (40%), spanning 0.152-23.022 Mb. Nineteen of the 24 CNVs were
confirmed with other techniques, whereas 5 changes were considered false positives (21%).
Fourteen of the confirmed CNVs were completely overlapping (74%) when the
oligonucleotide and SNP data were compared. In both analyses 8 patients showed a
deletion, 1 had two non-contiguous duplications on the same chromosome, while 2 had a
deletion and duplication on a single chromosome. These changes are assumed to be
pathogenic, based on their extent and the genes involved. SNP array results disclosed 5
CNVs not detected by array-CGH, including 3 deletions and 2 duplications, ranging in size
from 0.152 to 0.393 Mb, confirming that the higher density array is more sensitive in
detecting smaller CNV regions.
However, 3 of these CNVs did not contain known genes, questioning their pathogenic
role. In conclusion, the two tested platforms have proved to have good performance in
detecting possible causes of MR. Although the higher resolution of SNPs-array is capable
of deciphering disorders caused by small imbalances involving single genes, the higher rate
of false-positive results and the higher percentage of CNVs devoid of any clear pathogenic
role suggest a prudent use of this technique in the diagnostic practice.
16
NEUROFIBROMATOSIS TYPE 1: DEVELOPMENT
OF A NOVEL PROGRAM FOR MOLECULAR
DIAGNOSIS AND CLINICAL FOLLOW-UP
Donatella Bianchessi (a), Ettore Salsano (a), Francesca Orzan (a), Sara Guzzetti (a),
Veronica Saletti (b), Daria Riva (b), Federica Natacci (c), Gaetano Finocchiaro (a)
(a) Unità di Neuro-Oncologia Sperimentale, Fondazione IRCCS, Istituto Neurologico
Carlo Besta, Milano
(b) Unità Operativa di Neurologia dello Sviluppo, Fondazione IRCCS Istituto Neurologico
Carlo Besta, Milano
(c) Servizio di Genetica Medica, Fondazione IRCCS, Ospedale Maggiore Policlinico
Mangiagalli e Regina Elena, Milano
17
Thereafter patients will be clinically evaluated by at least one experienced neurologist
trained in NF1 every 6 or 12 months; visual acuity, fields and VEPs in children will be
performed every 6-12 months; MRI will be obtained every 5 years, also in absence of novel
signs (e.g., radicular pain, visual disturbances, etc.).
The program will start as of September 2008.
18
P. CYTOKINE-BASED IMMUNOTHERAPY
AND SUBVERSION OF TUMOR-RELATED
IMMUNOSUPPRESSION IN CUTANEOUS
AND OCULAR MELANOMA MODELS
Martina Borghi (a), Antonella Brizzolara (a), Tiziana Piazza (a), D. Rusciano (b), Paola
Queirolo (a), Carlo Mosci (a), Mario P. Colombo (c), Laura Borsi (a), Anna Rubartelli (a),
Silvano Ferrini (a)
(a) Istituto Nazionale per la Ricerca sul Cancro, IST, Genova
(b) Sooft Italia S.r.l., Montegiorgio, Ascoli Piceno
(c) Fondazione IRCCS, Istituto Nazionale dei Tumori, Milano
Ocular melanoma is a rare disease, with distinct clinical and biological features from the
more frequent cutaneous form as it develops predominantly liver metastases. Clinical
response rates to chemo or immunotherapy in metastatic melanoma have limited impact on
survival rates. We studied the development of new cytokine-based vaccine treatments
combined with antibodies blocking CD4+CD25+Foxp3+ regulatory T cells (Treg) in pre-
clinical models of metastatic melanoma.
The B16LS9 melanoma subline was previously derived from B16 cutaneous melanoma
by repeated passages of splenic injection and collection of liver metastases
(LS=liver/spleen). B16LS9 retain metastatic tropism for the liver when injected i.v. or in
the posterior eye chamber. To target GM-CSF to melanoma cells, we engineered GM-CSF
with an RGD peptide, which binds to the alpha-V/beta-3 integrins, with the aim to enhance
local immune-stimulating effects.
The GM-CSF ORF was chimerized at its 3' end with a synthetic RGD-encoding
sequence and cloned in an expression plasmid (pcDNA3.1hygro-RGD-GM-CSF), which
was transfected into B16F10 melanoma cells.
Transfected cells released biologically active GM-CSF/RGD (10ng/ml/24h/106 cells), as
detected by a proliferation assay on the GM-CSF-sensitive BAF3/GM subline. Part of the
GM-CSF/RGD was also displayed on the cell membrane of melanoma cells, as detected by
immunofluorescence with an anti-GM-CSF antibody.
Transfected B16F10 cells were then used as adjuvants by admixing them with B16LS9
cells as cellular vaccine for the immunotherapy of mice bearing B16LS9 metastases. By i.v.
injection, 100% of control mice developed lung and liver metastases within 25 days (mean
survival time 20.7±2.3), indicating that B16LS9 is a highly aggressive tumor.
Immunotherapy by administration of the irradiated cellular vaccine at day +2, +4, +7 +10,
+14 after initial tumor challenge induced only a slight increase in mean survival time
(22.9±4).
Therefore we speculated that the efficacy of the vaccine could be limited by either pre-
existing or tumor-induced Treg cells.
We then tried to combine this treatment with an anti-CD25 mAb (PC61, 0.5mg per
mouse), which targets Treg cells. Although the administration of anti-CD25 antibody alone
had no effect on tumor-free survival of mice bearing B16LS9 metastatic disease, when it
19
was combined with the cellular vaccine a highly significant increase in tumor-free survival
was observed (>41.1+9, P<0.0001), with about 30% of mice surviving for more than 45
days after primary challenge. We are now investigating other combinations which may
enhance the effectiveness of the vaccine, such as immunomodulating anti-OX40 mAb or a
TNF-alpha-scFv antibody targeting the melanoma extracellular matrix.
20
PUTATIVE ROLE OF MITOCHONDRIA
IN THE PATHOGENESIS OF SPINOCEREBELLAR
ATAXIA TYPE 1 (SCA1)
21
We found a severe cytochrome-c-oxidase deficiency in PuC of SCA1 mice that
interestingly parallels the severity and the progression of the disease during time.
Moreover, this oxidative stress contribute to trigger the mitochondrial apoptotic pathway
leading to specific Purkinje cell death.
22
TRANSCRIPTIONAL STUDY OF P63ALPHA MUTANTS
FOUND IN ECTODERMAL DYSPLASIA SYNDROMES
Eleonora Candi, Rita Cipollone, Andrea Codispoti, Gerry Melino, Alessandro Terrinoni
Laboratorio di Biochimica, IDI, Istituto Dermopatico dell'Immacolata, IRCCS, c/o
Dipartimento di Medicina Sperimentale e Scienze Biochimiche, Università degli Studi Tor
Vergata, Roma
23
EXPERIMENTAL CELL THERAPY IN OSTEOPETROSIS
Alfredo Cappariello (a,b), Anna C. Berardi (a), Barbara Peruzzi (b), Andrea Del Fattore (b),
Alberto Ugazio (a), Gian Franco Bottazzo (a), Anna Teti (b)
(a) Ospedale Pediatrico Bambino Gesù, IRCCS, Roma
(b) Università degli Studi, L'Aquila
24
GENETIC AND CLINICAL ASPECTS
OF RARE LYMPHOMAS
Elisabetta Caprini (a), Francesca Sampogna (a), Marcella Vicentini (c), Valeria Tocco (a),
Paolo Fadda (a), Isabella Quinti (c), Maurizio Carbonari (c), Marina Frontani (a), Giuseppe
Alfonso Lombardo (a), Damiano Abeni (a), Domenica Taruscio (b), Massimo Fiorilli (c),
Giandomenico Russo (a)
(a) IDI, Istituto Dermopatico dell'Immacolata, IRCCS, Roma
(b) Centro Nazionale Malattie Rare, Istituto Superiore di Sanità, Roma
(c) Dipartimento di Medicina Interna e Immunologia Clinica, Università degli Studi La
Sapienza, Roma
25
were fatigue, pain, and insomnia. The differences among CL types were particularly high
in the global health status and emotional functioning scales, with a worse HRQoL in
patients with SS, followed by MF, and CBCL. HRQoL impairment in all CL types was
higher in women than in men, in patients with probable anxiety or depression, and during
worsening of the disease.
26
DEVELOPMENT OF NEW DIAGNOSTIC APPROACHES
FOR TRANSMISSIBLE SPONGIFORM
ENCEPHALOPATHIES
Franco Cardone (a), Serena Principe (a), Piero Parchi (b), Gianluigi Zanusso (c), Salvatore
Monaco (c), Fabrizio Tagliavini (d), Maurizio Pocchiari (a)
(a) Dipartimento di Biologia Cellulare e Neuroscienze, Istituto Superiore di Sanità, Roma
(b) Dipartimento di Scienze Neurologiche, Università degli Studi, Bologna
(c) Dipartimento di Scienze Neurologiche e della Visione, Università degli Studi, Verona
(d) Dipartimento di Neuroscienze Cliniche, Fondazione IRCCS, Istituto Neurologico Carlo
Besta, Milano
27
different electrophoretic migration) with a significant association between disease
phenotype and relative abundance of each type.
Although preliminary, the results obtained so far already allowed an updated
classification of sCJD variants and may contribute to formulate an early differential
diagnosis with other dementias.
28
DYSREGULATED RAS SIGNALING IN NOONAN
SYNDROME AND RELATED DISORDERS:
DISEASE GENE DISCOVERY
AND FUNCTIONAL STUDIES
Claudio Carta (a), Viviana Cordeddu (a), Elisabetta Flex (a), Valentina Fodale (a),
Francesca Pantaleoni (a), Valentina Petrangeli (a), Paola Torreri (a), Francesca Lepri (b),
Giuseppe Zampino (c), Maria C. Digilio (d), Luisa Castagnoli (e), Tamara C. Petrucci (a),
Anna Sarkozy (b), Bruce D. Gelb (f), Simone Martinelli (a), Lorenzo Stella (g), Bruno
Dallapiccola (b), Marco Tartaglia (a)
(a) Dipartimento di Biologia Cellulare e Neuroscienze, Istituto Superiore di Sanità, Roma
(b) Ospedale Casa Sollievo della Sofferenza, IRCCS, San Giovanni Rotondo, Foggia, e
Istituto Casa Sollievo della Sofferenza Mendel, Roma; Università degli Studi Sapienza,
Roma
(c) Istituto di Clinica Pediatrica, Università Cattolica del Sacro Cuore, Roma
(d) Genetica Medica, Ospedale Pediatrico Bambino Gesù, IRCCS, Roma
(e) Dipartimento di Biologia, Università degli Studi Tor Vergata, Roma
(f) Center for Molecular Cardiology, Mount Sinai School of Medicine, New York, NY, USA
(g) Dipartimento di Scienze e Tecnologie Chimiche, Università degli Studi Tor Vergata,
Roma
Noonan Syndrome (NS) and the clinically related LEOPARD Syndrome (LS) are
genetically heterogeneous Mendelian traits characterized by short stature, facial
dysmorphisms, cardiac defects, and variable skin and skeletal anomalies. Increased RAS-
MAPK signal traffic due to heterozygous PTPN11 and KRAS mutations cause 50% of NS,
while a bunch of amino acid changes impairing PTPN11/SHP2's catalytic activity account
for 90% of LS.
Major goal of this project was to identify novel NS/LS disease genes. By using a
candidacy approach focused on genes coding transducers with role relevant to RAS
signalling, we discovered SOS1, RAF1 and BRAF as novel genes implicated in NS/LS
pathogenesis. SOS1 encodes a RAS-specific GEF. SOS1 mutations account for 10% of NS,
cluster at residues implicated in the maintenance of its autoinhibited conformation, and
promote enhanced RAS-MAPK activation. The phenotype associated with SOS1 defects is
distinctive, with a high prevalence of ectodermal abnormalities but normal cognitive
development and growth. RAF1 and BRAF mutations were identified in a small percentage
of NS and LS. These genes encode serine/threonine protein kinases functioning as RAS
effectors. Most RAF1 mutations altered a motif that is critical for protein autoinhibition
through 14-3-3 binding, and promoted enhanced ERK activation. RAF1 mutations in two
hotspots were strongly associated with hypertrophic cardiomyopathy. BRAF mutations
mapped to multiple protein domains, and largely did not overlap with cardiofaciocutaneous
syndrome-causing or cancer-associated defects. Selected BRAF mutations promoted
variable gain of function of the kinase, but appeared less activating compared than the
oncogenic V600E protein.
29
A second major goal of this project was to characterize functionally a panel of NS/LS-
causing PTPN11 mutations. Specifically, we investigated the mechanisms underlying the
invariant occurrence of the T42A, E139D and I282V substitutions in NS, and the Y279C
and T468M changes in LS. We demonstrated that the Ile-to-Val change at codon 282 is the
only substitution at that position perturbing the stability of PTPN11/SHP2's closed
conformation without impairing catalysis, while the Thr-to-Ala change, but not other
substitutions of codon 42, promotes increased phosphopeptide binding affinity.
The recognition specificity of the C-SH2 domain bearing the E139D substitution differed
substantially from its WT counterpart acquiring binding properties similar to those observed
for the N-SH2 domain, revealing a novel mechanism of SHP2's functional dysregulation.
Finally, we identified the deamination of the methylated cytosine at nucleotide 1403 as the
driving factor leading to the high prevalence of the T468M change in LS.
30
INHERITED EPIDERMOLYSIS BULLOSA:
MOLECULAR FINDINGS, DIAGNOSTIC
GUIDELINES AND QUALITY OF LIFE EVALUATION
Daniele Castiglia (a), Marco Castori (a), Claudia Covaciu (a), Marina D'Alessio (a),
Claudia Uras (b), Stefano Tabolli (b), Marina Colombi (c), May El-Hachem (d), Paolo
Salerno (e), Domenica Taruscio (e), Giovanna Zambruno (a)
(a) Laboratorio di Biologia Molecolare e Cellulare, IDI, Istituto Dermopatico
dell'Immacolata, IRCCS, Roma
(b) IDI, Istituto Dermopatico dell'Immacolata, IRCCS, Roma
(c) Divisione di Biologia e Genetica, Università degli Studi, Brescia
(d) Divisione di Dermatologia, Ospedale Pediatrico Bambino Gesù, IRCCS, Roma
(e) Centro Nazionale Malattie Rare, Istituto Superiore di Sanità, Roma
31
experience greater difficulties, especially for the physical components. Concerning the
family burden of disease the mean values observed are not as high as expected.
Finally, a multidisciplinary, multispecialty task force of experts was convened under the
coordination of the National Centre Rare Diseases of the National Health Institute to
develop and validate national guidelines for the diagnosis of EB.
32
DEVELOPMENT OF AN EPIDEMIOLOGICAL
AND MOLECULAR INTEGRATED APPROACH
FOR THE PREVENTION OF CONGENITAL
HYPOTHYROIDISM: PRELIMINARY RESULTS
Roberto Cerone (a), Mario De Felice (b), Roberto Di Lauro (b,c), Emanuela Medda (d),
Luca Persani (e), Domenica Taruscio (f), Massimo Tonacchera (g), Antonella Olivieri (h)
(a) Dipartimento di Pediatria, Università degli Studi, Istituto Giannina Gaslini, Ospedale
Pediatrico IRCCS, Genova
(b) IRGS, Biogem, Ariano Irpino, Napoli
(c) Stazione Zoologica Anton Dohrn, Napoli
(d) Centro Nazionale di Epidemiologia, Sorveglianza e Promozione Salute, Istituto
Superiore di Sanità, Roma
(e) Dipartimento di Scienze Mediche, IRCCS Istituto Auxologico Italiano, Università degli
Studi, Milano
(f) Centro Nazionale Malattie Rare, Istituto Superiore di Sanità, Roma
(g) Dipartimento di Endocrinologia, Università degli Studi, Pisa
(h) Dipartimento di Biologia Cellulare e Neuroscienze, Istituto Superiore di Sanità, Roma
33
for CH with thyroid dysgenesis. As concerns CH with eutopic thyroid, 21 unrelated patients
with this form of CH and a Partial Iodide Organification Defect (PIOD) were studied.
In these patients genes coding for Dual Oxidases (DUOX1 and DUOX2) and DUOX
maturation factors (DUOXA1 and DUOXA2) were screened and for the first time a
DUOXA2 defect in a Chinese female with CH, PIOD and mild permanent hypothyroidism
during childhood was found. Moreover, the analysis of the coding-region of DUOX2 gene
in further 10 CH children with eutopic thyroid, identified 6 new mutations involving exon
22, exon 17, exon 23, exon 24, and exon 21.
Finally, for what concerns molecular basis of thyroid disgenesis, 143 DHTP/bc mice
were genotyped using 235 Single Nucleotide Polymorphisms (SNPs).
Analysis of genotyping data revealed two chromosomal regions associated to CH: one
on Chr 2 (with a LOD score of 11.2) and another on Chr 5 (with a LOD score of 2.5). 800
genes have been mapped on region of Chr 2 associated to the CH phenotype; about 400 of
these are expressed in the thyroid. By using SNPs analysis 2 new candidate genes have
been identified: calpain 3 and Dnajc17.
34
CHARACTERIZATION OF HIPK2
THAT BY ASSOCIATING WITH MECP2 MIGHT
FUNCTION AS A MODIFIER GENE
IN RETT SYNDROME
Barbara Conca (a), Giorgia Bracaglia (b), Fabiola Moretti (c), Charlotte Kilstrup-Nielsen (a),
Nicoletta Landsberger (a), Silvia Soddu (b)
(a) Laboratorio del Controllo Genetico ed Epigenetico dell'Espressione, Università degli
Studi dell'Insubria, Busto Arsizio, Varese
(b) Dipartimento di Oncologia Sperimentale, IFO, Istituti Fisioterapici Ospitalieri, Istituto
Nazionale Tumori Regina Elena, IRCCS, Roma
(c) Istituto di Neurobiologia e Medicina Molecolare, Consiglio Nazionale delle Ricerche,
Roma
35
pattern of the two proteins in the brain of adult mice is highly similar. We therefore
believe that these studies are relevant for understanding whether this novel MeCP2
interactor acts as a modifier gene influencing disease severity in RTT patients with
mutations in MeCP2.
36
microRNA EXPRESSION PROFILE
OF PARATHYROID CARCINOMAS
Sabrina Corbetta (a), Valentina Vaira (b), Alfredo Scillitani (c), Vito Guarnieri (c), Cristina
Eller-Vainicher (d), Iacopo Chiodini (d), Salvatore Minisola (e), Paolo Beck-Peccoz (d),
Silvano Bosari (b), Anna Spada (d)
(a) IRCCS Policlinico San Donato, Università degli Studi, San Donato Milanese, Milano
(b) Azienda Ospedaliera San Paolo, Polo Universitario, Università degli Studi, Milano
(c) Ospedale Casa Sollievo della Sofferenza, IRCCS, San Giovanni Rotondo, Foggia
(d) Fondazione IRCCS, Ospedale Maggiore Policlinico Mangiagalli e Regina Elena,
Università degli Studi, Milano
(e) Università degli Studi La Sapienza, Roma
The pathogenesis of parathyroid cancer remains unclear. Recently, the loss of the
oncosuppressor HPRT2 gene product, parafibromin, has been demonstrated to be
involved in the Hyperparathyroidism-Jaw Tumor (HPT-JT) syndrome and in a
consistent set of sporadic parathyroid carcinomas. This finding highlighted the role of
the Wnt/beta-catenin pathway in parathyroid carcinogenesis. Nonetheless, detailed
understanding of parathyroid oncogenesis would facilitate addressing scientific and
clinical challenging. MicroRNAs (miRNAs) are a new class of small, noncoding RNAs
implicated in development and cancer. A deregulated miRNA can orchestrate the
aberrant expression of several target genes.
The aim of the present study was to identify deregulated miRNAs in parathyroid
cancers compared to normal parathyroid tissues. We performed a low-density array-based
profiling of 4 parathyroid cancers and two normal parathyroid biopsies. All carcinomas
showed a mutation in HPRT2 gene and were negative for parafibromin immunostaining.
Out of 362 human miRNAs assayed, 279 (77%) were expressed above background levels in
all samples. Hierarchical clustering based on the expression of these miRNAs correctly
classified the normal specimens from the tumors. For all expressed miRNAs, we calculated
Fold Change ratios (FC) between normal and tumoral parathyroid specimens on median
normalized RQs. As threshold for significant different expression, we set FC=5 or 0.2, for
over or down-expression, respectively.
At the indicated cut-off, 15 miRNAs were significantly down-expressed, while just 3
miRNAs displayed a statistically significant overexpression in all parathyroid cancer
specimens. SAM analysis setting the minimum fold change for log-transformed data at 2.5
and maximum q-value at 49.1%, identified hsa-miR-296 and 139 being negatively related
with tumor presence and hsa-miR-503 and 222 being up-regulated in parathyroid
carcinomas. In particular, miR-296 was able to discriminate between parathyroid cancers
and normal glands (p=0.0012) with a null misclassification rate at the cross-validation
procedure. To further investigate the expression of hsa-miRNA-296, we analyzed its
expression profile in 13 parathyroid sporadic adenomas, 4 atypical adenomas and 2
metastasis. Hsa-miRNA-296 expression levels were definitely low in parathyroid cancers
and metastasis as well as in atypical adenomas, while in sporadic adenomas they were
reduced but not significantly different from normal samples. In conclusion, we identified a
37
set of 4 miRNAs differently expressed in parathyroid carcinomas versus normal
parathyroids. In particular, the down-regulated has-miRNA-296 was shown to distinguish
unequivocally between parathyroid carcinomas and adenomas. Further studies are needed
to define the target genes of has-miRNA-296 in parathyroid tissue and its regulation.
38
P. ORPHAN DRUGS: GENERAL DEFINITION
AND RELEVANCE FOR THE DERMATOLOGIST
Orphan drugs are defined as those products not distributed by the pharmaceutical industry
because they are not commercially viable even if they meet a general public health need.
However, a substance used in the treatment of a frequent disease may also have an as yet
undeveloped use as orphan product.
In real terms, orphan drugs fall under the following categories: i) products aimed at the
treatment of rare diseases; ii) products taken off the market for commercial or therapeutic
reasons; iii) products that have not been developed. At present, the issue of orphan drugs is
under consideration in the case of rare diseases.
In Europe, a rare disease is one which affects no more than 5 on 10,000 individuals.
The WHO has so far classified 5,000 rare pathologies for the most part caused by genetic
anomalies. In these pathologies, diagnosis is the first problem that has to be faced but a
second problem is what approach to adopt in terms of therapy. One of the greatest obstacles in
ensuring suitable treatment for these patients is the pharmaceutical industry's unwillingness to
develop drugs at normal marketing conditions because, in the absence of incentives, the costs
of the process would not be recovered from sales.
The development of drugs for rare diseases has been concentrated in certain areas
(particularly cancer and metabolic diseases) whereas no or few drugs have been approved for
other areas including those of interest for dermatologist. This is unfortunate because rare
diseases are present in dermatology and so this issue is of importance to the practitioner.
39
GENOTYPE-PHENOTYPE CORRELATIONS
IN THE CMT NEUROPATHIES:
DEFINITION OF A CLINICAL AND GENETIC
DIAGNOSTIC FLOW-CHART
Silvia Coviello (a), Alessio Colombo (b), Sara Benedetti (b), Ivana Spiga (b), Federica
Cerri (c), Marina Scarlato (c), Raffaella Fazio (c), Giancarlo Comi (c), Maurizio Ferrari (b,d),
Stefano Previtali (c), Alessandra Bolino (a), Angelo Quattrini (c)
(a) Istituto Dulbecco Telethon, Roma
(b) Laboratorio di Biologia Molecolare Clinica, Diagnostica e Ricerca, Fondazione San
Raffaele del Monte Tabor, IRCCS, Milano
(c) Dipartimento di Neurologia, Fondazione San Raffaele del Monte Tabor, IRCCS, Milano
(d) Unità per la Diagnosi Genomica delle Malattie Umane, Fondazione San Raffaele del
Monte Tabor, IRCCS, Milano
40
52% of demyelinating cases (79% with positive family history), 38% of axonal (71% in
familial cases) and 19% in intermediate CMTs (17% in familial cases). We also identified
five new mutations in the following genes: MPZ (D224Y), EGR2 (D383H), MFN2
(A738V), GDAP1 (P59fsX61), HSP27 (S135C).
41
IDENTIFICATION OF miRNA/TARGET GENE PAIRS
INVOLVED IN HEREDITARY BREAST CANCER
Elisabetta Crippa (a,b), Lara Lusa (a,b), Loris De Cecco (a,b), James F. Reid (a,b),
Siranoush Manoukian (a), Paolo Radice (a,b), Carlo M. Croce (c), Marco A. Pierotti (a,b),
Manuela Gariboldi (a,b)
(a) Fondazione IRCCS, Istituto Nazionale dei Tumori, Milano
(b) Fondazione Istituto di Oncologia Molecolare, IFOM, Fondazione Italiana per la
Ricerca sul Cancro, FIRC, Milano
(c) Comprehensive Cancer Centre, Ohio State University, Columbus, OH, USA
We performed a transcriptome analysis of coding and non coding RNAs (miRNA) from
a group of BRCA1, BRCA2, BRCAX (familial cases with no mutations in BRCA1 or
BRCA2 genes) and sporadic breast cancers using the microarray technology for identifying
possible miRNA dependent mechanisms involved in this we tumor type.
We identified 106 genes (P<0.005) and 100 miRNAs (P<0.05) that were differentially
expressed between the groups of familial and sporadic breast cancers included in our study.
In particular gene expression analysis confirmed the strong difference between BRCA1
group and the other cases, while miRNA analysis highlighted the prevalent expression of
these molecules in the sporadic cases. Cluster analysis of the samples showed that the
BRCAX group consisted of two sub-groups, one similar to sporadic tumors, the other with
characteristics similar to the group of patients with BRCA1 mutations. These results were
observed both for coding and non coding transcripts, thus supporting the genuine existence
of the two sub-groups.
To identify miRNA-target gene pairs deregulated in breast cancer we integrated the two
analyses. First we searched the public databases for the putative miRNA regulators
(predicted to bind complementary sequences) of the genes we found differentially
expressed among our breast cancer groups. We then confirmed their presence in the
miRNA lists we generated from our expression profiling. We identified 24 miRNA
inversely correlated with 76 genes. We focused on one pair differentially expressed
between Estrogen Receptor (ER)-positive and ER-negative cases and involving a gene
whose expression is known to be inversely correlated to that of ER.
This gene has also been proposed as a negative regulator of BRCA1 and its possible
regulatory miRNA was highly expressed in the BRCAX sub-group that exhibited the
characteristics of BRCA1-mutant cases. QRT-PCR analysis on a panel of breast cancer cell
lines and on 293T cells confirmed the inverse expression of this putative pair. We
functionally validated the interaction observed by cloning the 3' UTR sequence of the gene
containing the predicted miRNA binding site in a luciferase reporter construct in 293T cell
line. We are testing the role of this miRNA in breast cancer by transfecting it in breast
cancer cell lines and analyzing changes in expression of the endogenous target gene, as
well as of BRCA1 and ER.
42
INNOVATIVE BURKITT'S LYMPHOMA THERAPY
Giovanna Cutrona (a), Serena Matis (a), Maria Rita Mariani (a), Michele Cilli (b), Federica
Piccardi (b), Antonio Daga (c), Gianluca Damonte (d), Enrico Millo (d), Michele Moroni (f),
Silvio Roncella (f), Franco Fedeli (f), Lidia C. Boffa (a), Manlio Ferrarini (a,e)
(a) Oncologia Medica C, Istituto Nazionale per la Ricerca sul Cancro, IST, Genova
(b) Servizio di Sperimentazione su Modelli Animali, Istituto Nazionale per la Ricerca sul
Cancro, IST, Genova
(c) Servizio di Oncologia Sperimentale F, Istituto Nazionale per la Ricerca sul Cancro,
IST, Genova
(d) DIMES, Sezione di Biochimica e Centro di Eccellenza per la Ricerca in Biochimica,
Università degli Studi, Genova
(e) Dipartimento di Oncologia, Biologia e Genetica, DOBiG, Università degli Studi,
Genova
(f) Unità Operativa di Anatomia ed Istologia Patologica, ASL5, La Spezia
Burkitt's Lymphoma (BL), one of the most aggressive human cancers, is a very rare
malignancy in the Western world (sporadic form), while is frequent among children from
areas like Central Africa (endemic form). Systemic chemotherapy, the present treatment of
choice for BL at all stages, has high toxicity and has an overall survival rate correlated to
the stage of the disease at diagnosis and concomitant pathologies (e.g. HIV-seropositivity).
Most BL are characterized by t(8;14, 2 or 22) chromosomal translocations juxtaposing
the c-myc oncogene to the Ig loci.
Consequently c-myc becomes up regulated by the now proximal Eµ enhancer, at the
5'of the Ig locus, promoting cell hyper proliferation. We previously demonstrated that, in
BL cells with the t(8;14) translocation, a Peptide Nucleic Acid (PNA) complementary to
the intronic Eµ sequence (PNAEµ) specifically inhibited expression of the translocated c-
myc and caused in vitro cell growth arrest.
We recently completed a series of test required to enter PNAEµ in phase I/II in patients,
like -definition of pharmacokinetics (including the persistence of the therapeutically active
portion of PNAEµ) and lack -of toxicity in an in vivo model system, -of immunogenicity in
immunocompetent mice, -of mutagenicity or clastogenicity (as detectable by standard assays).
We initially studied a BL model of SCID mice inoculated s.c. with BRG-BL cells.
This model presented the advantage of developing easily detectable and measurable
tumors. We demonstrated that chronic administration of PNAEµ to these mice, already
inoculated with BL cells, caused: increased latency of tumor appearance, relevant decrease
of final tumor size and necrosis.
However the efficacy of PNAEµ needed to be tested in a model more similar to the
human adult sporadic form of BL. BRG-BL cells were transfected with the firefly
luciferase gene and inoculated i.v. into SCID mice giving origin to disseminated
lymphomas. BL cells growth was detected in mice upon i.p. injection with D-Luciferin with
an IVIS Xenogen imaging system. Bioluminescent signals from BRG-BL-Luc cells, as
captured by the camera system, were recorded, integrated, digitalized, displayed, and
quantified (in photons/second) using the Living Image program.
43
With this type of analysis we determined that treatment with PNAEµ specifically
caused significant inhibition of BL cell expansion as confirmed by inspection at necropsy.
In particular a reduced invasion was apparent at the main sites of BL cell growth (similar to
the human BL): peritoneal fat, brain and rachis. Altogether, the data support the potential
therapeutic value of PNAEµ in Burkitt's Lymphoma.
44
NOVEL EXPERIMENTAL APPROACHES
FOR INVESTIGATION ON NEW THERAPIES
AGAINST RARE HUMAN BONE TUMORS
Angelo De Milito (a), Francesco Lozupone (a), Rossella Canese (b), Maria Marino (a),
Franca Podo (b), Stefano Fais (a)
(a) Dipartimento del Farmaco, Istituto Superiore di Sanità, Roma
(b) Dipartimento di Biologia Cellulare e Neuroscienze, Istituto Superiore di Sanità, Roma
Human bone malignancies including Osteosarcoma (OS) and Ewing's Sarcoma (ES),
are rare tumors in both adults and children, characterized by a high biologic aggressiveness.
The strategy of treatment is based on a combined modality of surgery and
chemotherapy. Chemotherapy (a combination of 4 drugs), is delivered before and after
surgical removal of the tumor (neoadjuvant chemotherapy).
However, the most recent improvements in the cure rate of patients with localized
disease have been achieved by dose-intensification, in turn paying the price of acute severe
toxicity and secondary malignancies. Moreover, 35% of patients show tumor resistance to
systemic therapies and treatments for high-risk patients are still completely inadequate and
no new drugs have reported to be really active and useful in sarcomas.
Thus, innovative treatment modalities are indeed very welcome and needed. In this project
we proposed some in vitro and in vivo models, to evaluate potential new therapeutic strategies
aimed at inhibiting the growth and metastatic behaviour of human bone tumors. The first
issue of the project was to investigate the significance of ezrin in bone malignancies.
Moreover, we investigated expression and function of V-ATPases in osteosarcoma and
Ewing's sarcoma cell lines. We also performed experiments aimed at analyzing molecular
composition of microvesicles released from bone-marrow malignancy cells. Virtually
conclusive data have shown that ezrin is involved in many activities of bone marrow
malignancies, including multidrug resistance and microvesicle release. The data definitively
show that ezrin is instrumental for a full function of Pgp-1 in Osteosarcoma (OS) MDR cells.
In fact, ezrin was linked to Pgp-1 exclusively in MDR cells, as compared to parental sensible
cells. In turn this linkage is related to the membrane localization of Pgp-1.
Through the use of a deletion mutant of ezrin we transfected the MDR OS cells, showing
that overexpression of a small inefficient ezrin leads to loss of function of MDR cells, that
become sensible to chemotherapeutics and loose Pgp-1 membrane expression. As far as Pgp-
1 is concerned we found this protein expressed on MDR OS released microvesicles.
Moreover, also V-ATPases have shown to participate to the malignant behaviour of rare
bone tumors and some V-ATPases inhibitors have proven to interfere with the metastatic
potential of these tumors. MRI-guided MRS approaches have shown that bone marrow
malignancies are clearly acidic and that inhibition of V-ATPases activity, through Proton
Pump Inhibitors (PPI) increase the pH of these tumors. Consistent with PPI effect on tumor
acidity we also found both increased sensibility of OS tumors to in vivo treatment with PPI
in terms of both chemosensibilization and a direct antineoplastic effect. Lastly, treatment of
an extensive panel of osteosarcoma and Ewing's sarcoma cell lines bone-tumors derived
45
cells with small molecule inhibitors against IGF-IR or c-src, recently identified as specific
tyrosin kinase inhibitors, have shown to be effective in inhibiting the tumor cell growth.
Altogether these preliminary results suggest that ezrin and proton pumps may represent
newly-identified molecular targets for new therapeutic strategies against rare bone
malignancies.
46
GENOTYPE/PHENOTYPE ANALYSIS
OF NEURODEGENERATIVE AND AGING-PRONE
SYNDROMES CAUSED BY MUTATIONS
IN THE DNA DAMAGE RESPONSE/REPAIR PATHWAY
Domenico Delia (a), Annapaola Franchitto (b), Pietro Pichierri (b), Margherita Bignami (b),
Luciana Chessa (c)
(a) Fondazione IRCCS, Istituto Nazionale dei Tumori, Milano
(b) Dipartimento di Ambiente e Connessa Prevenzione Primaria, Istituto Superiore di
Sanità, Roma
(c) Università degli Studi La Sapienza, Roma
47
employing to immunoprecipitate endogenous SETX complexes for mass spectrometry
analysis and identification of SETX-interacting proteins.
As for A-T, in a collaborative study, we have set up an immunofluorescence analysis
ATM phosphorylation that coupled with flow cytometry allows quick diagnose of A-T
patients and A-T heterozygotes directly from resting peripheral blood lymphocytes.
48
INNOVATIVE MANAGEMENT OF PATIENTS
WITH DIFFUSE MALIGNANT PERITONEAL
MESOTHELIOMA: CLINICAL-DIAGNOSTIC
PATHWAY AND NEW THERAPEUTIC TARGETS.
PRELIMINARY RESULTS
Marcello Deraco (a), Nadia Zaffaroni (c), Federica Perrone (b), Dario Baratti (a), Raffaella
Villa (a), Shigeki Kusamura (a), Genny Jocollé (b), Antonello D. Cabras (b), Silvana Pilotti (b)
(a) Dipartimento di Chirurgia, Fondazione IRCCS, Istituto Nazionale dei Tumori, Milano
(b) Dipartimento di Patologia, Fondazione IRCCS, Istituto Nazionale dei Tumori, Milano
(c) Dipartimento di Oncologia Sperimentale, Fondazione IRCCS, Istituto Nazionale dei
Tumori, Milano
49
No PI3KCA mutations were found, while all DMPMs showed expression of PTEN and
expression/activation of AKT, ERK, mTOR and S6.
Conclusions. CRS+HIPEC is associated to encouraging survival results. Both telomere
maintenance mechanisms, telomerase activity and ALT are present in DMPM and
differentially affect prognosis. EGFR, PDGFRA and PDGFRB are promising molecular
targets for tailored treatments.
50
P. CHARACTERIZATION OF Wnt/β-CATENIN
PATHWAY, IGF-2 METHYLATION STATUS,
MIR PROFILES AND CELL SIGNALLING
IN HEPATOCARCINOMA AND HEPATOBLASTOMA
CELL LINES
Alessandra Di Masi (a), Sara Nicolai (a), Marco Salvatore (b), Mara Viganotti (b), Fabrizio
Tosto (b), Stefano Lorenzetti (c), Francesca Maranghi (c), Roberta Tassinari (c), Gianluca
Azzalin (d), Armando Magrelli (d), Alberto Mantovani (c), Domenica Taruscio (b),
Giuseppe Macino (d), Caterina Tanzarella (a), Antonio Antoccia (a)
(a) Università degli Studi Roma Tre, Roma
(b) Centro Nazionale Malattie Rare, Istituto Superiore di Sanità, Roma
(c) Dipartimento di Sanità Pubblica Veterinaria e Sicurezza Alimentare, Istituto Superiore
di Sanità, Roma
(d) Sezione di Genetica Molecolare, Dipartimento di Biotecnologie Cellulari ed
Ematologia, Policlinico Umberto I, Roma
Hepatocellular Carcinoma (HCC) and Hepatoblastoma (HB) are two hepatic cancers
characteristic of the adulthood and childhood, respectively. The high mortality
associated with these diseases is mainly attributed to the inability to diagnose HCC and
HB at early stages.
Several signalling pathways, such as Wnt/β-catenin and Insulin-like Growth Factors
(IGFs), have been associated with the pathogenesis and prognosis of several tumours.
Wnt/β-catenin signalling pathway controls cell proliferation and body patterning
throughout development; IGF-2 gene expression is crucial for normal development, being
highly expressed in foetal liver, and its concentration declining after birth. Alterations in
the Wnt signalling pathway and/or mutations in β-catenin encoding gene, are involved in a
high percentage of human HCC and HB. Furthermore, dysregulation of normal IGF-2 gene
promoters usage, also due to DNA methylation status, has been observed in several cancers,
including HB.
The aim of this study was to identify new molecular markers for HCC and HB, by
investigating the gene, protein and microRNA expression profiles in HCC (Hep3B, HepG2,
HLE), and in HB (HUH6) human cell lines, in comparison to human primary hepatocytes.
Furthermore, IGF-2 methylation status of its different promoters was examined.
To this end, the expression of 113 genes involved in the Wnt/β-catenin pathway was
analysed by microarray. As a common pattern of the hepatic cancerogenesis, a significant
modulation in the expression of 8 genes was observed in all tested tumour cell lines
analysed, as compared to normal hepatocytes. In particular, 4 genes were up-regulated
(FZD7, NLK, RHOU, SOX17) and 4 were down-regulated (TCF7L2, TLE1, SLC9A3R1 e
WNT10A), as also confirmed by qRT-PCR.
The microRNA profiles are markedly altered in cancers and some of them have a causal
role in tumorigenesis. Among them we focused on the expression of microRNA-21
51
oncogene, finding that it was overexpressed in the cell lines compared to normal
hepatocytes, while the liver-specific microRNA-122 was downregulated. Downregulation
of microRNA-122 is associated with hepatocarcinogenesis as described elsewhere.
Surprisingly, we found that microRNA-483, located in chromosome 11p15 in one of the
IGF2 gene intron, was finely regulated.
To assess the role of IGF2 gene and microRna 483 the methylation status of the four
different IGF2 promoters, was analysed by Methylation Specific PCR (MSP): in particular
we focused on promoters 2, 3 and 4. Overall promoter-specific levels of IGF2 transcription
has been evaluated by qRT-PCR. Dysregulation of pleiotropic anti-apoptotic proteins,
growth factors, receptors and their downstream components represent a central pro-
tumorigenic principle in human hepatocarcinogenesis. In order to perform a global
molecular characterization of the four HCC and HB cell lines, the expression of 224
proteins that covers biological pathways such as apoptosis, cell cycle, and signal
transduction was analysed using a protein array system. The protein expression profiles
were significantly different among the four cell lines analysed. The commonly modulated
ones were 8 proteins: 4 proteins belong to the cell cycle category (c-Abl, Cdc25, Cdk4, and
Ciclin D3), 2 to the cytoskeleton category (Cytokeratin 4 and 13), 1 to apoptosis (DAPK
pS308), and 1 to signal trasduction (GRB-2). Protein modulation was confirmed by Western
blot analysis.
In conclusion, by gene, protein and microRNA expression profiling, several possible
molecular markers for HCC and HB have been identified. In particular, the increased GRB-
2 expression observed in the cell lines analysed seems to be particularly interesting due to
its possible role in the genesis of other types of tumours.
This work is performed within the frame of the project "Tackling rare diseases yet lacking
diagnosis and/or prognosis: a pilot project integrating data collection and experimental studies"
supported by a NIH-ISS 2007-2009 grant.
52
AUTOIMMUNE PEMPHIGUS (AP): DYNAMICS
OF AUTOREACTIVE B CELLS AND QUALITY
OF LIFE EVALUATION
Biagio Didona, Giovanni Di Zenzo, Stefano Tabolli, Giuseppe Cianchini, Damiano Abeni,
Giovanna Zambruno, Antonio Lanzavecchia
IDI, Istituto Dermopatico dell'Immacolata, IRCCS, Roma
AP is a rare but life-threatening bullous disease of the skin and mucous membranes. AP
is mediated by autoantibodies against keratinocyte cell surface antigens, desmoglein 1 and
3 (Dsg1 and Dsg3). To study the repertoire of autoreactive memory B cells in AP patients
at various disease stages (untreated, corticosteroid-treated, in remission) and following
rituximab treatment for severe disease, we have applied a previously developed method for
the efficient immortalization of human B cells. Several human Monoclonal Antibodies
(MAbs) reactive for various epithelial antigens were cloned: 19 anti-Dsg3 and/or Dsg1
MAbs and 16 MAbs recognizing different keratinocyte antigens.
The MAbs have been characterized by: i) ELISAs based on Dsg1 and Dsg3 ectodomain;
ii) staining of different epithelial tissues and cell substrates; iii) immunoblotting and
immunoprecipitation analysis using keratinocyte extracts.
Seven of the anti-Dsg Mabs were IgG4 and 12 used kappa light chain, 14 stained live
HaCaT with an intercellular pattern and 10 stained at least one of the analyzed tissues.
Preliminary data indicate periplakin and a ≅100 kDa protein as possible targets of MAbs
recognizing epithelial antigens other than Dsg1/3. The pathA recognising Dsg1/3 as well as
other epithelial antigens could represent valuable tools for disease diagnosis and for
investigating mechanisms of blister formation in AP.
In parallel we have focused on the analysis of AP natural history and of the effects of
disease and therapy burden on Quality of Life (QoL) and psychological status. a set of
instruments for qol evaluation has been routinely used for all ap cases followed in our
institute (220 patients enrolled). Hospitalized patients received the sf-36, skindex-29 and
GHQ-12 questionnaires and reported on the perceived severity of disease. In parallel,
disease severity was assessed using the Physician Global Assessment (PGA) and the ikeda
scoring system. A preliminary analysis of the first 139 patients showed strong impact of ap
on health status especially in women, older subjects and patients with mucocutaneous
lesions. A significant correlation between disease severity and lower sf-36 values was also
noted. AP patients presented a markedly impaired overall QoL compared with healthy
controls on all three skindex-29 scales (p<0.001). Disease severity was also significantly
associated with all three skindex-29 scale scores, for both pga and ikeda values (p<0.05). A
high percentage of patients presented psychiatric non psychotic symptoms. overall, the
introduction in daily clinical activities of QoL evaluation instruments has been helpful,
adding more information for clinical reporting and patient management.
53
P. THE ITALIAN EXTERNAL QUALITY ASSESSMENT
(EQA) IN GENETIC TESTS: THE VI EQA SCHEME
Vincenzo Falbo, Giovanna Floridia, Marco Salvatore, Manuela Marra, Fabrizio Tosto,
Federica Censi, Domenica Taruscio
Centro Nazionale Malattie Rare, Istituto Superiore di Sanità, Roma
The Italian External Quality Control (EQC) started in 2001 at the Istituto Superiore di
Sanità. The following four EQC disease schemes are offered: Cystic Fibrosis (CFTR gene),
Beta-Thalassemia (Hbb gene), Fragile-X syndrome (FMR1 gene), the Adenomatous
Polyposis Coli (APC gene); the cytogenetics scheme covers prenatal, postnatal and
oncological diagnosis.
82 Public laboratories have been enrolled on a voluntary basis, distributed on the
National territory. Five trials have been performed and concluded. Results showed that
there has been an improvement in the use and the interpretation of molecular genetic tests.
The average genotyping error rate observed over the five years was 0.6%, 0.3%, 5% and
4.7% in the Cystic Fibrosis, Beta-Thalassemia, Fragile-X syndrome and Adenomatous
Polyposis Coli scheme respectively.
The percentage of complete reports in cytogenetics increased over the period. However,
lack of information or inadequacy in reporting are still observed. On the other hand, as has
been indicated in other international surveys for quality assessment, it will be only after
several years of testing experience and participation in quality assessment schemes that a
significant reduction in laboratory errors will be possible.
On the basis of the experience acquired until now and in order to harmonize the activity
of our schemes with existing European ones, we have developed a web-based system that
has been used for the VI trial. A total of 96 Public laboratories have been enrolled by
website through an account, with an increase of about 17% compared to V trial. In
particular: i) 30 laboratories out of 96 were registered for cytogenetics; ii) 36 for molecular
genetics; iii) 30 for cytogenetics and molecular genetics.
The number of respondents was: 46/49 (94%) for Cystic Fibrosis; 22/23 (96%) for Beta-
Thalassemia; 17/21 (81%) for Fragile-X syndrome; 6/6 (100%) for Adenomatous Polyposis
Coli; 28/33 (85%) for oncological cytogenetics; 37/43 (86%) for prenatal diagnosis; 48/55
(87.3%) for postnatal diagnosis.
The section of the web-based system restricted to the Steering Committee and assessors
is in progress in order to develop a more clear marking system, either in molecular genetics
and in cytogenetics, to better identify the performance of laboratories.
This work has been funded in the frame of the Projects "Genetic testing for rare diseases:
additional development in the Italian External Quality Assessment Programme", "Programma di
collaborazione ISS-NIH, Area Malattie Rare" Fasc. 7LR1, Cap. 526.
54
RESEARCH PROJECT "INFANT BOTULISM":
THE FIRST TWELVE MONTHS
Lucia Fenicia (a), Fabrizio Anniballi (a), Dario De Medici (a), Elisabetta Delibato (a),
Davide Lonati (b), Carlo Locatelli (b)
(a) Centro Nazionale di Riferimento per il Botulismo, Dipartimento di Sanità Pubblica
Veterinaria e Sicurezza Alimentare, Istituto Superiore di Sanità, Roma
(b) Centro di Controllo Veleni e Centro Nazionale di Informazione sulla Tossicologia,
Unità di Tossicologia, Fondazione Salvatore Maugeri, IRCSS, Università degli Studi,
Pavia
In the frame on the bilateral Italy (ISS)-USA (NHI, Office for Rare Diseases) agreement
on joint research and development of public health actions on rare diseases, "Infant
Botulism" project was developed. Infant Botulism (IB) is an orphan (rare) disease that
affect infants aged less than one year. From 1976 to 2007 less than 3,500 cases were
worldwide recognized. Despite Italy reported the largest number of cases in Europe, the
disease is little known and diagnoses are made mainly by clinicians who have a familiarity
with the illness. The main objectives of this project are to improve knowledge of the
disease in Italy by training physicians to the suspicious and improving public awareness,
standardization of a therapeutic protocol, inclusion of the illness in the Italian National
Register of Rare Diseases. The project started on 1st May 2007, is structured in three work
packages: WP1-Educational program; WP2-Diagnostic methods; WP3-National Reference
Center for Botulism (NRCB), Website on Infant Botulism.
During the first year of work, WP1 developed educational courses to evaluate the
medical knowledge of IB. Sixteen Scientific Societies were involved. Written and web-
version questionnaire were submitted to physicians. Typical case with a clinical syndrome
of IB was described and the specific answers regarding clinical management and
differential diagnosis were posed. Preliminary results showed that only 6% of physicians
consider IB as first diagnosis. An entire session dedicated to botulism particularly in
infants, was also included in "Antidotes in Depth 2008 and Chemical Emergencies Clinical
and Public Health Issues", International Continuing Education Course in Clinical
Toxicology (Pavia, October 14-18). Medical information will be distributed with two
different types of brochures addressed to medical staff, public and parents.
About diagnostic methods (WP2), the use of molecular methodologies were
investigated in order to have a rapid diagnosis of the cases. Extraction and purification of
DNA from Botulinum Neurotoxin (BoNT) producing Clostridia strains were optimized.
Multiplex gel-based PCR and SYBR Green Real Time PCR were successful utilized to
detect respectively bont/A, bont/B, bont/E, bont/F genes and bont/A gene. In order to
develop a Multiplex probe-based Real Time PCR, all bont sequences reported in GeneBank
were submitted to in silico analysis to detect best primers and probes. Since the genoma of
BoNT-producing Clostridia containing a low percentage of C/G, MGB and LNA probe
were chose.
About WP3, the procedure to obtain BabyBIG in Italy and link between the Infant
Botulism Treatment and Prevention Program (IBTPP) and NRCB websites were defined.
55
MYH9: POSSIBILITIES FOR A NUCLEAR ROLE
56
MOLECULAR MODELING OF NIPBL MISSENSE
MUTATIONS: AN ADJUNCT TOOL
FOR THE COMPREHENSION
OF GENOTYPE-PHENOTYPE CORRELATIONS
Serena Ferraiuolo (a), Maura Masciadri (a), Cristina Gervasini (b), Paola Castronovo (b),
Angelo Selicorni (c), Donatella Milani (c), Lidia Larizza (a,b), Silvia Russo (a)
(a) Laboratorio di Citogenetica e Genetica Molecolare Umana, IRCCS Istituto Auxologico
Italiano, Milano
(b) Divisione di Genetica Medica, Azienda Ospedaliera San Paolo, Polo Universitario,
Università degli Studi, Milano
(c) Dipartimento di Pediatria, Fondazione IRCCS, Ospedale Maggiore Policlinico
Mangiagalli e Regina Elena, Milano
57
CHARACTERIZATION OF GENETIC
AND CYTOGENETIC ALTERATIONS
IN SALIVARY GLAND TUMORS
Giovanna Floridia (a), Federica Censi (a), Manuela Marra (a), Stella Lanni (a), Maria Pia
Foschini (b), Vincenzo Falbo (a), Domenica Taruscio (a)
(a) Dipartimento di Biologia cellulare e Neuroscienze, Istituto Superiore di Sanità, Roma
(b) Sezione di Patologia, Ospedale Bellaria, Università degli Studi, Bologna
This work has been funded in the frame of the Project "Salivary gland tumors: different
approaches to identify genetic and prognostic markers" Fasc 7GR1, Programma di collaborazione
ISS-NIH, Area Malattie Rare.
58
A GENOME WIDE NON-SYNONYMOUS SNP SCAN
OF AMYOTROPHIC LATERAL SCLEROSIS (ALS)
Isabella Fogh (a), Antonia Ratti (b), Cinzia Gellera (c), Ferdinando Squittieri (d), John
Powell (a), Vincenzo Silani (b)
(a) Institute of Psychiatry, Department of Neuroscience, MRC Center Neurodegeneration
Research, London, UK
(b) Dipartimento di Scienze Neurologiche, IRCCS Istituto Auxologico Italiano, Università
degli Studi, Milano
(c) Fondazione IRCCS, Istituto Neurologico Carlo Besta, Milano
(d) Centro Malattie Rare, Dipartimento di Neurogenetica, Neuromed, IRCCS, Istituto
Neurologico Mediterraneo, Pozzilli, Isernia
Background. Only 15% ALS patients have a family history, the remaining cases
occurring sporadically in the human population. While familial ALS is well characterized
with several causative genes identified to date, the genetics of sporadic ALS is poorly
understood. In the past year three independent Genome-Wide Association (GWA) studies
found no single gene strongly associated with susceptibility to ALS suggesting a complex
interaction between environmental factors and many susceptibility genes of small effect
best describes this disease. One such susceptibility gene of small effect recently nominated
by a GWA study from different populations of European origin is Dipeptidyl-Peptidase 6
(DPP6) which slightly increases the risk of developing ALS (OR 1.3).
Aims. To confirm the association of DPP6 with ALS phenotype we tested the candidate
polymorphism rs10260404 in an Italian population.
Methods. The Italian cohort included 907 cases and 1019 healthy controls collected by
the first "Italian ALS Consortium" created by the collaboration of several Neurological
Centres located in North Italy. All the DNA samples have been gathered at the Italian
Auxologico Institute in 96-well bar-coded plates and quantified with PicoGreen fluorescent
reagent (Invitrogen). Clinical information about ALS patients has been placed in a shared
database according to the International form already used for the US and UK GWA studies
so that genotype-phenotype correlations will be easily inferred from this database. All ALS
cases had any recorded family history were previously screened for Zn/Cu superoxide
dismutase1, alsin, angiogenin and TAR DNA binding protein genes.
Results. Assuming an OR of 1.3 with a causative allele frequency of 0.44, as described
by the authors, we have >99% power to detect an association with a p value of 0.05.
Our preliminary data show no evidence of association of rs10260404 SNP with
susceptibility to ALS (Fisher's exact chi-square test p=0.8). Moreover, genotype scores
were tested for Association with Age at Onset (AAO), available for 743 cases (457 males,
286 females). AAO ranged from 15 to 84 years with mean 55.22 and median 57 years (sd
13.5). Kaplan-Meier survival analysis showed no significant association (Log Rank chi-
squared 3.72, p 0.155, 2df) between variant rs10260404 genotypes and AAO and no
differences for genders were detected.
Conclusion. Polymorphism rs10260404 in DPP6 gene, as other variants reported to be
associated with sporadic ALS, has failed to be replicated in a different population. These
59
results highlight the genetic heterogeneity of sporadic ALS even within European
populations. The same conclusions have been drawn for many complex diseases and
emphasize the importance of large sample sizes and international collaborations for a meta-
analysis of different studies.
60
NEUROLOGICAL IMPAIRMENT IN NIEMANN-PICK C
DISEASE: A STUDY ON THE ROLE OF EXCITATORY
NEUROTRASMITTER RECEPTORS
AND IDENTIFICATION OF PERIPHERAL
CELLULAR BIOMARKERS
Claudio Frank (a), Daniele Grossi (c), Giovanna De Chiara (b), Mauro Racaniello (b),
Giuseppe Biagini (e), Virginia Tancredi (c), Stefano Rufini (d), Daniela Merlo (b),
Giovanna D'Arcangelo (c)
(a) Dipartimento del Farmaco, Istituto Superiore di Sanità, Roma
(b) Dipartimento di Biologia Cellulare e Neuroscienze, Istituto Superiore di Sanità, Roma
(c) Dipartimento di Neuroscienze, Università degli Studi Tor Vergata, Roma
(d) Dipartimento di Biologia, Università degli Studi Tor Vergata, Roma
(e) Dipartimento di Scienze Biomediche, Università degli Studi di Modena e Reggio Emilia,
Modena
Changes in the functioning of neuronal plasma membranes are good candidates in the
research of Niemann-Pick Disease type C (NPDc) pathophysiogenetic mechanisms. The
loss of a correct dynamic of cholesterol-sphingolipids-enriched microdomains in the
neuronal and glial plasma membrane, caused by an imbalance in the lipid trafficking due to
NPDc gene mutation, might have a key role in neuronal dysfunction and the consequent
clinical pathologies. Our previous results suggest that changes in the plasma membrane
cholesterol content are particularly important in affecting lipid rafts, regulators of glutamate
receptor functioning. We therefore evaluated through several experimental approaches
whether the physiological properties and the neurotransmission of NPC neurons show
differences from what observed in the Wild Type (WT).
To this aim acute brain slices, primary neuronal cell cultures and synaptosomal
preparation from WT and NPC mice, a well-established mouse model for the Niemann-
Pick type C disease, were used; in some experiments the Methyl-beta-Cyclodextrin
(MbetaCD), a molecule that dissolves the hydrophobic core of lipid rafts, was perfused.
The electrophysiological data suggest an impairment of the excitatory neurotransmitter
receptors, since a different response to kainic acid perfusion was observed: in fact in
hippocampal slices from NPC mice the excitotoxic effect properly described for the WT
slices was lacking.
These data are in agreement with the results of WT MbetaCD-treated slices which
respond to kainic acid application that partially resembles the NPC slices trend, confirming
that lipid rafts manipulation counteracts kainate effect. Moreover the induction and
maintenance of NMDA-dependent LTP in the CA1 region of NPC hippocampal slices were
significantly reduced. The electrophysiological results are supported by data outcoming
from cell culture experiments on excitatory aminoacid-induced intracellular calcium
increase. Indeed, application of both NMDA and kainic acid in WT cell culture treated with
MbetaCD significantly reduced calcium influx. Moreover, results from Western Blot
analysis on synaptosomal membrane fractions revealed that levels of GluR6/7 kainate
61
receptor subunits were about 30% reduced in synaptosomes from NPC slices as compared
to wild-type.
In order to develop a method for a rapid and suitable diagnosis, we used some fibroblast
cell lines obtained from patients. Cell lines have been maintained in culture and the lipid
composition was determined with standard procedures. Finally, we used different strategies
to correlate sphingolipid/cholesterol membrane content with the pathological status of the
fibroblast donor, based on the ability of some toxins to bind cell lipids. The results obtained
encourage more detailed studies.
62
GENETIC, MOLECULAR AND FUNCTIONAL
CHARACTERIZATION OF COCKAYNE SYNDROME,
A RARE TRANSCRIPTION/REPAIR DEFECTIVE
HEREDITARY DISEASE
Guido Frosina (a), Eugenia Dogliotti (b), Elena Botta (c), Angelo Calcagnile (b), Gianluigi
Casartelli (a), Paolo Degan (a), Mariarosaria D'Errico (b), Mara Foresta (a), Tiziana Lemma (b),
Laura Narciso (b), Tiziana Nardo (c), Roberta Oneda (c), Donata Orioli (c), Ilaria Pettinati (a),
Monica Ropolo (a), Miria Stefanini (c)
(a) Unità di Mutagenesi Molecolare e Riparazione del Danno al DNA, Istituto Nazionale
per la Ricerca sul Cancro, IST, Genova
(b) Dipartimento di Ambiente e Connessa Prevenzione Primaria, Istituto Superiore di
Sanità, Roma
(c) Istituto di Genetica Molecolare, Consiglio Nazionale delle Ricerche, Pavia
63
range, being able to repair AP sites, 8-oxopurines and fapy purines. Expression of FPG
totally reversed the 8-oxoguanine repair defect in CS cells. hence fpg may be a suitable
candidate for relieving the 8-oxopurine repair defect in cs patients. similar studies are under
way with the E. coli endonuclease III (NTH) protein that efficiently repairs oxidized
pyrimidines. these complementation studies may shed light on lesions relevant for the CS
phenotype and offer new therapeutic options.
64
A DOUBLE-BLIND PLACEBO-CONTROLLED
CLINICAL TRIAL ADDRESSING THE INHIBITION
OF PDGFR PHOSPHORYLATION
AS A CANDIDATE PATHOGENETIC TREATMENT
OF SYSTEMIC SCLEROSIS
Armando Gabrielli (a), Giovanni Pomponio (a), Paolo Fraticelli (a), Michele Luchetti (a),
Silvia Svegliati (a), Gianluca Moroncini (a), Roberto Giacomelli (b), Paola Cipriani (b),
Alessandra Marrelli (b), Vasiliki Liakouli (b), Elisa Pingiotti (b), Vincenza Dolo (b),
Danilo Millimaggi (b), Sandra D'Ascenzo (b), Ilaria Giusti (b), Serena Guiducci (c), Marco
Matucci-Cerinic (c), Sergio Generini (c), Gianfranco Ferraccioli (d), Barbara Tolusso (d),
Maria De Sanctis (d), Walter Malorni (e), Anna Maria Giammarioli (e), Elisabetta Straface (e),
Marina Pierdominici (e), Angela Maselli (e), Laura Somma (e), Serena Vettori (f),
Giuseppina Abignano (f), Gabriele Valentini (f), Patrizia Rovere-Querini (f), Stefano
Franchini (g), Angelo Andrea Manfredi (g), Maria Grazia Sabbadini (g)
(a) Università degli Studi, Ancona
(b) Università degli Studi, L'Aquila
(c) Università degli Studi, Firenze
(d) Università Cattolica del Sacro Cuore, Roma
(e) Dipartimento del Farmaco, Istituto Superiore di Sanità, Roma
(f) Università degli Studi Napoli 2, Napoli
(g) Università Vita-Salute San Raffaele, Fondazione San Raffaele del Monte Tabor, IRCCS,
Milano
65
for 6 months (+6 months of follow-up) in addition to the conventional treatment. The
preliminary authorization for the study has been recently obtained by the Ethical.
Committee of the San Raffaele Scientific Institute, the coordinating center, and other
authorization requests are pending. Primary outcome measures include the evaluation of: i)
the safety of Imatimib administered in low dose in SSc patients; ii) the efficacy of imatinib
to improve sclerodema skin disease by assessment of skin thickness evaluated by the
modified Rodnan skin score, which reflects skin fibrosis; iii) the amelioration of the quality
of life and the patient physical and emotional well being, evaluated by HAQ (Italian
version) and SF-36 score. Secondary outcomes will be: i) the capacity of the drug to revert
in vitro the functional alterations of the SSc fibroblasts (Ros generation, collagen
production, PDGFr phosphorylation) appraised on skin biopsies obtained prior to treatment,
at the end of treatment and after 3 and 6 months of follow-up; ii) the efficacy of imatinib on
pulmonary interstitial disease, assessed by pulmonary function test, Diffusing Lung Carbon
Oxide, six minute walk test, and high-resolution CT scan.
66
FOR A DEFINITION AND A LIST OF RARE CANCERS
IN EUROPE
Gemma Gatta (a), Laura Ciccolallo (a), Stefano Ferretti (b), Lisa Licitra (a), Paolo Casali (a),
Paolo Angelo Dei Tos (c), Riccardo Capocaccia (d)
(a) Fondazione IRCCS, Istituto Nazionale dei Tumori, Milano
(b) Registro Tumori di Ferrara, Università degli Studi, Ferrara
(c) Ospedale di Treviso, ASL 2 Veneto, Treviso
(d) Centro Nazionale di Epidemiologia, Sorveglianza e Promozione della Salute, Istituto
Superiore di Sanità, Roma
The burden of rare tumours is not known, both in Europe and in Italy. For this reason,
two projects have been funded to estimate the basic epidemiologic indicators of frequency
(incidence, prevalence and mortality) and outcome (survival) for rare cancers in Europe and
Italy. The first step of both projects is to provide a definition of rare malignancies and an
exhaustive list of them.
Our contribution will describe the methodology followed to reach an international
agreement on a definition and list of rare cancers that will permit to identify the rare entities
for which the indicators will be calculated.
The International Classification of for Oncology (ICD-O) is the tool utilised for the
definition of the tumour entities. Population-based cancer registries are the basis for both
the calculation of the indicators and the definition of the threshold. An international group
of experts was formed in order to reach an agreement for an operative definition and a
definitive list of rare malignant tumours. Three important elements were discussed within
the experts: the indicator of frequency, the entity and the threshold.
With respect of indicator of frequency, the group of experts, mainly clinicians from
the ESMO Faculty, agreed that incidence is the most appropriate indicators for rare
cancers. Tumour entities were defined by combinations between morphology and
topography. The provisionally identified threshold is 3/100,000/year range under which
a tumor might be reasonably considered as rare. Incidence was calculated as crude rate
from pooled European data.
Other criteria such as age, sex, clinical presentation and biological features were not
considered for the definition of the rare entities. The final definition and list will circulate
during the summer among the experts and all the partners of the projects in order to reach a
final agreement.
67
ADIPOSE TISSUE-DERIVED STEM CELLS
FOR THE TREATMENT OF MUSCULAR DYSTROPHY
Ilaria Gatto (a), Antonietta Gentile (a), Gabriele Toietta (a), Maurizio C. Capogrossi (a,b),
Giuliana Di Rocco (b)
(a) Laboratorio di Patologia Vascolare, IDI, Istituto Dermopatico dell'Immacolata,
IRCCS, Roma
(b) Laboratorio di Biologia Vascolare e Terapia Genica, Centro Cardiologico Monzino,
IRCCS, Milano
68
Pitx2 CONTROLS BETA-CATENIN mRNA STABILITY
69
PATHOGENETIC ROLE OF ISOLATED
HUMAN TSC2 SMOOTH MUSCLE CELLS
AND ITS PHARMACOLOGICAL CONTROL.
NOVEL PERSPECTIVES IN TSC AND LAM
Alfredo Gorio, Elena Lesma, Silvano Bosari, Stephana Carelli, Anna Maria Di Giulio
Dipartimento di Medicina, Chirurgia e Odontoiatria, Facoltà di Medicina, Università degli
Studi, Sezione di Farmacologia Clinica, Istituto Clinico Humanitas, IRCCS, Rozzano,
Milano
70
MESENCHYMAL STEM CELLS FOR THE TREATMENT
OF TIBIAL CONGENITAL PSEUDARTHROSIS
ASSOCIATED WITH TYPE I NEUROFIBROMATOSIS
Donatella Granchi (a), Valentina DeVescovi (a), Elisa Leonardi (a), Serena R. Baglio (a),
Onofrio Donzelli (b), Marina Magnani (b), Armando Giunti (a), Nicola Baldini (a)
(a) Laboratorio per la Patofisiologia dell'Impianto Ortopedico, Istituti Ortopedici Rizzoli,
IRCCS, Bologna
(b) Dipartimento di Ortopedia Pediatrica, Istituti Ortopedici Rizzoli, IRCCS, Bologna
Type 1 Neurofibromatosis (NF1), the most common single gene disorder found in
humans, is the main cause of Tibial Congenital Pseudarthrosis (TCP). The treatment of
TCP consists on repeated surgical procedures which often fail with the inevitable outcome
of severe disability. The use of autologous bone Marrow Stromal Cells (MSC) has been
recently proposed, because the MSC pool contains osteogenic precursors, that in turn may
enhance bone repair. In the 1st year of the project our preliminary results showed that the
osteogenic potential of MSCs was higher in Iliac Crest (IC-MSC) than in the Pseudarthrosis
site (P-MSC), suggesting that the autologous MSC transplantation may be a promising
strategy for improving bone consolidation where traditional techniques fail. In the 2nd year
we planned to complete the sample collection, and to test whether bone microenvironment
may affect the osteogenic potential of IC-MSC. Bone fragments from pseudarthrosis lesion
were collected from each patient in order to obtain primary osteoblast culture (HOB). HOB
and MSC from the same individual were used in a co-culture system in order to mimic the
interaction between microenvironment (HOB) and osteoprogenitors (MSC). We enrolled 5
patients affected by NF1 and TCP (TCP-NF1+; 4M/1F, age 0.7-16 yrs), 6 patients affected
by TCP without NF1 (TCP-NF1-; 5M/1F, age 2.6-18 yrs), and 2 healthy male donors (5
and 7.5 yrs). Both IC-MSC and P-MSC were cultured in osteogenic medium containing α-
MEM, 10% fetal bovine serum (FBS) or 10% autologous serum (AUT), 10-8M
dexamethasone, and 50 μg/mL ascorbic acid. The ability to generate bone-forming cells
was tested by measuring cell proliferation, alkaline phosphatase activity, mineral nodule
formation, and gene expression, and it was higher in IC-MSC than in P-MSC cultures, even
though significant differences were observed only in TCP-NF1+. In these patients, the in
vitro mineralization of IC-MSC was reduced by AUT serum, since the number of mineral
nodules was similar to that observed in P-MSC. Generally, the osteogenic potential of IC-
MSC was lower in patients than in healthy donors. The co-cultures were performed in 7/11
patients, and the preliminary results suggested that the osteogenic differentiation of IC-
MSC was affected by HOBs derived from pseudarthrosis, but the proliferation seemed to be
inhibited only in TCP-NF1+. These findings imply that bone microenvironment could
influence negatively the success of the autologous MSC transplantation, and further studies
have to be performed to better understand the mechanism by which that occurs.
The study was performed with the collaboration and contribution of Istituto Superiore di Sanità
(Programma Italia-USA "Malattie Rare") and "Io ci sono" Association.
71
P. NEURAL TUBE DEFECTS AND FOLIC ACID:
AN INTEGRATED, EVIDENCE-BASED APPROACH
TO PRIMARY PREVENTION IN THE ITALIAN CONTEXT
Michele Grandolfo (a), Domenica Taruscio (b), Alberto Mantovani (c), Sonia Brescianini (a),
Pietro Carbone (b), Marco Salvatore (b)
(a) Centro Nazionale di Epidemiologia, Sorveglianza e Promozione della Salute, Istituto
Superiore di Sanità, Roma
(b) Centro Nazionale Malattie Rare, Istituto Superiore di Sanità, Roma
(c) Dipartimento di Sanità Pubblica Veterinaria e Sicurezza Alimentare, Istituto Superiore
di Sanità, Roma
72
are reachable in populations in which general food fortifications is being performed, a
precautionary approach is recommended toward such procedure, at least in anticipation of
further studies. On the other hand, in order to prevent neural tube defects it is advisable to
effectively support strategies such as the promotion of a more proper nutrition and the
periconceptional supplementation.
Our effort for the future will be based on the implementation of strategy for the promotion
of FA supplementation (including targeted actions towards potentially vulnerable groups) thus
estimating whether their influence on NTDs trend prevalence. Furthermore, the strength of
association between the FA supplementation and multiple pregnancy will be estimated.
73
TGFBR1 AND TGFBR2 GENE MUTATIONS
IN LOEYS-DIETZ AND THORACIS AORTIC
ANEURYSM DISSECTION SYNDROMES
Maurizia Grasso (a), Nicola Marziliano (a), Eliana Disabella (a), Alessandra Serio (a),
Michele Pasotti (a), Fabiana Gambarin (a), Andrea Pilotto (a), Elena Serafini (a), Marta
Diegoli (b), Emanuele Porcu (a), Marilena Tagliani (a), Monica Concardi (a), Manuela
Agozzino (a), Pamela Cassini (a), Berabra Di Giorgio (a), Eloisa Arbustini (a)
(a) Centro Malattie Genetiche Cardiovascolari, Fondazione IRCCS Policlinico San
Matteo, Pavia
(b) Università degli Studi, Pavia
Mutations in the TGFBR1 and TGFBR2 genes cause the autosomal dominant Loeys-
Dietz Syndromes (LDS). Based on the presence or absence of cranio-facial traits the
syndromes are classified as LDS 1 and LDS 2, respectively.
We performed clinical and molecular characterisation of 92 members of 29 families
whose probands were addressed to our attention with the suspected diagnosis of Marfan
Syndrome (n=25) and familial Thoracic Aortic Aneurysm and Dissection (TAAD) (n=4).
Probands and realtives underwent genetic counselling, multidisciplinary clinical and
imaging evaluations and molecular analysis of the FBN1 (n=25) TGBFR1 and TGRBR2
genes (n=29).
We found 31 TGFBR1&2 mutations in 29 probands; two carried a double
heterozygosity, one inherited and one de novo. 23 relatives carried the corresponding
proband's mutation. Based on phenotypical ground 29/52 mutations carriers were diagnosed
with LDS1 and 23 with LDS2.
The two syndromes shared aortic aneurysm (93% and 91%), high rate of dissection
(27% and 38%), arterial tortuosity (100%) and, at a minor rate, aneurysms of other vessels
(45% and 29%) and skin/integumental traits. The disease was de novo in 53% of the
probands with LDS1 and 4% of probands with LDS2. The mean age at first diagnosis was
18.44±17.14 (<1-46) and 40.78±15.56 (14-68), at first surgery 24.53±14.17 (1-46) and
44.61±14.55 (18-69), with 42 interventions in 28 patients. Congenital heart defects and
cranio-facial, skeletal, ocular, and nervous system traits typically recurred in LDS1.
The LDS1 and LDS2 severely affect the cardiovascular system, with arterial tortuosity
as common maker shared by the two syndromes.
74
THE SIGNIFICANCE OF SURGICAL TECHNIQUES
EVOLUTION IN THE TREATMENT OF DEFORMITIES
ASSOCIATED TO RARE DISEASES:
SCOLIOSIS IN PRADER-WILLI SYNDROME
75
MOLECULAR ANALYSIS OF ARSA AND PSAP
GENES IN TWENTY-ONE ITALIAN PATIENTS
WITH METACHROMATIC LEUKODYSTROPHY.
IDENTIFICATION AND FUNCTIONAL
CHARACTERIZATION OF 11 NOVEL ARSA ALLELES
Serena Grossi (a), Stefano Regis (a), Camillo Rosano (b), Alessandra Biffi (c), Fabio
Corsolini (a), Maria Sessa (c,d), Mirella Filocamo (a)
(a) Laboratorio Diagnosi Pre-Postnatale Malattie Metaboliche, Istituto Giannina Gaslini,
Ospedale Pediatrico IRCCS, Genova
(b) Unità di Bioinformatica e Proteomica Strutturale, Istituto Nazionale per la Ricerca sul
Cancro, IST, Genova
(c) Istituto Telethon per la Ricerca sul Gene, Milano
(d) Unità di Neurologia, Fondazione San Raffaele del Monte Tabor, Milano
76
folding of the protein, whereas the replacement of Y376N is expected to leave a solvent-
accessible surface area in proximity of a cluster of hydrophobic residues with consequent
destabilization and/or incorrect folding of the protein.
The present study is aimed at providing a broader picture of the molecular basis of
MLD Italian population. Our findings demonstrate and confirm the necessity of a
comprehensive evaluation, based on a range of diagnostic procedures including
neuroradiological, neurophysiological, biochemical and molecular tests, to shed light on the
underlying pathological causes of MLD.
77
FAMILY BASED TRANSMISSION ANALYSIS
OF GENETIC MARKERS IN CLASS I
AND CLASS III HLA REGION IN SARDINIAN
CHILDREN WITH AUTISTIC SPECTRUM DISORDERS
Franca R. Guerini (a), Elisabetta Bolognesi (a), Sonia Usai (b), Salvatorica Manca (b),
Mario Clerici (a,c)
(a) Laboratorio di Medicina e Biotecnologie Molecolari, Fondazione Don C. Gnocchi
Onlus, Centro IRCCS S. Maria Nascente, Milano
(b) Istituto di Neuropsichiatria Infantile, Università degli Studi, Sassari
(c) Dipartimento di Scienze Biomediche e Biotecnologiche, Università degli Studi, Milano
78
SOX7 AND -17 FUNCTION AS MODIFIERS
OF THE LYMPHANGIOGENIC ROLE OF SOX18.
NEW INSIGHTS IN THE PATHOGENESIS
OF THE HUMAN SYNDROME HYPOTRICHOSIS-
LYMPHEDEMA-TELANGIECTASIA
Brett Hosking (a), Mathias François (a), Andrea Caprini (b), Fabrizio Orsenigo (b),
Francesco Bertolini (d), Elisabetta Dejana (b,c), Peter Koopman (a)
(a) Institute for Molecular Bioscience, The University of Queensland, Brisbane, Australia
(b) Fondazione Istituto di Oncologia Molecolare, IFOM, Fondazione Italiana per la
Ricerca sul Cancro, FIRC, Milano
(c) Dipartimento di Scienze Biomolecolari e Biotecnologiche, Scuola di Scienza, Università
degli Studi, Milano
(d) Fondazione IEO, Istituto Europeo di Oncologia, Milano
In the previous work within this program, we found that the transcription factor SOX18
is required for activating endothelial transcription of Prox1, thus initiating the lymphatic
endothelial program of development from blood vascular precursors.
Mutations in SOX18 result in lymphatic dysgenesis in the human syndrome
Hypotrichosis-Lymphedema-Telangiectasia (HLT). However, the phenotype of Sox18-null
mutant mice produced by gene targeting varies dramatically depending on the background
strain. In the following work we found that two closely related Group F SOX factors,
SOX7 and SOX17, are upregulated in the absence of SOX18 during the genesis of the
lymphatic vasculature, on a mixed genetic background but not on a C57BL/6 background.
Like SOX18, SOX7 and -17 are also able to activate Prox1 transcription in vitro, in
cultured cells and in transgenic mice. Our results indicate that SOX7 and -17 act as strain-
specific modifiers of the lymphangiogenic role of SOX18. These data may explain the
variability of clinical manifestations of the rare human syndrome HLT.
79
NEW FINDINGS FROM MECP2-308 AND KFL7 MICE
AS MODELS OF MENTAL RETARDATION
Giovanni Laviola (a), Laura Ricceri (a), Bianca De Filippis (a), Carla Perrone-Capano (b),
Maria Giuseppina Miano (b)
(a) Dipartimento di Biologia Cellulare e Neuroscienze, Istituto Superiore di Sanità, Roma
(b) Istituto di Genetica e Biofisica, Consiglio Nazionale delle Ricerche, Napoli
Supported by Italy-USA Program on Rare Disease "X-linked or autosomal rare mental retardation
syndromes: phenotypic analysis in transgenic mouse models" and by ERARE-EuroRETT Network.
80
MEASUREMENT OF NAD(P)H AUTOFLUORESCENCE
BY VIDEO-MICROSCOPY IN EX-VIVO AND IN VITRO
MODELS OF AMYOTROPHIC LATERAL SCLEROSIS
(ALS) AND DISEASES CONNECTED
WITH MITOCHONDRIAL CONDITIONS
Stefano Loizzo (a), Andrea Fortuna (a), Rosalba Carozzo (b), Sergio Visentin (c), Cecilia
Prata (d), Alberto Loizzo (a)
(a) Dipartimento del Farmaco, Istituto Superiore di Sanità, Roma
(b) Ospedale Pediatrico Bambino Gesù, IRCCS, Roma
(c) Dipartimento di Biologia Cellulare e Neuroscienze, Istituto Superiore di Sanità, Roma
(d) Istituto di Biochimica G Moruzzi, Università degli Studi, Bologna
This project was financed in part by ISS-NIH Joint Research Project on Rare Diseases.
81
P. PROPOSAL FOR AN INTEGRATED
APPROACH TO RARE DISEASES:
A STUDY BETWEEN BASIC LABORATORY MODELS
AND CLINICAL EPIDEMIOLOGY
IN AMYOTROPHIC LATERAL SCLEROSIS (ALS)
Stefano Loizzo (a), Alberto Loizzo (a), Maria Masocco (b), Lorenza Nisticò (b), Paolo
Salerno (c), Domenica Taruscio (c), Nicola Vanacore (b), Monica Vichi (b)
(a) Dipartimento del Farmaco, Istituto Superiore di Sanità, Roma
(b) Centro Nazionale di Epidemiologia, Sorveglianza e Promozione della Salute, Istituto
Superiore di Sanità, Roma
(c) Centro Nazionale Malattie Rare, Istituto Superiore di Sanità, Roma
82
Possible twins are being identified linking the Italian Twin Registry to ALS patients
lists provided by 3 ALS regional Registries and 14 diagnosis Reference Centres. So far,
among 4,982 patients (60% males), diagnosed with "definite", "probable" or "possible"
ALS since 1990, we ascertained 29 twins (none of them belong to the same pair) plus 18
patients whose twin status is under ascertainment.
Twenty-two ALS twins (15 males) are from same sex pairs and 7 (6 male) belong to
unlike sex pairs. As regards living status, in 1 pair both twins (ALS twin and co-twin) are
deceased, while in 15 pairs 14 ALS twins and 1 co-twin are deceased. Health status or
cause of death of co-twins will be ascertained by a neurologist. Life exposure to putative
ALS risk factors will be investigated through a co-twin control study. Collection of
biological material from ALS and unaffected twins is also envisaged.
WP4: NAD(P)H transient technique in ex-vivo and in vitro models for the studies of
Amyotrophic Lateral Sclerosis (ALS) and diseases connected with mitochondrial
conditions. Farmacologia della salute della donna e del bambino, Dipartimento del
Farmaco, Istituto Superiore di Sanità.
We evidenced a consistent alteration of NAD(P)H autofluorescence levels in G93A
brain slices, and also in recycling pattern following ultraviolet stimuli in cellular models.
These results indicate a new investigation procedure, in that our investigation equipment
can be applied not only to ex-vivo brain slices, but also to peripheral, non-neuronal cells,
and can give interesting information for the studies of metabolic conditions connected with
mitochondrial diseases.
83
P. NEEDS OF PEOPLE INVOLVED IN RARE DISEASES
Anna Maria Luzi (a), Anna Colucci (a), Barbara De Mei (b), Pietro Gallo (a), Chiara
Cattaneo (b), Rossella Petrigliano (c), Domenica Iacono (c), Antonella Sanseverino (c),
Italian Patient's Associations for Rare Diseases, Domenica Taruscio (c)
(a) Dipartimento di Malattie Infettive, Parassitarie ed Immunomediate, Istituto Superiore
di Sanità, Roma
(b) Centro Nazionale di Epidemiologia, Sorveglianza e Promozione della Salute, Istituto
Superiore di Sanità, Roma
(c) Centro Nazionale Malattie Rare, Istituto Superiore di Sanità, Roma
Rare diseases represent about 10% of known human pathologies and affect a relevant
part of the Italian population. Among the problematic experiences faced by the people
dealing with these kind of pathologies, communication and relationships should draw
particular attention. On this topic the National Centre for Rare Diseases of the "Istituto
Superiore di Sanità" started a pilot project "Effective communication and counselling:
Improving listening in rare diseases". This is a national, multicentric and pilot experience of
cooperation among different subjects. The project of two years duration has the following
goals: i) to identify the planning criteria for the communication process in rare diseases,
and to improve the scientific and technical expertise; ii) to implement more diffused and
comprehensive communicative procedures based on integration and participation models;
iii) to favour a cooperative network exchange among people involved in rare diseases.
The study involves health workers working for the National Health Service and/or
charities and implies four phases.
Phase 1: this phase is about setting up and actualising a qualitative study. This is
achieved by activating focus groups made of health workers, representatives of associations
of patients, patients themselves and their relatives. The objectives was to identify the real
needs and the critical areas of management of rare diseases. Each focus group was made up
of a facilitator, an observer and 10-12 participants had a duration of 90 minutes and was
video-recorded upon explicit and informed consent.
Contents were typed on a computerised system and eventually were analysed in order
to: i) identify areas of strength and critical areas in the communication; ii) identify the
needs of those directly or indirectly involved in the field of rare diseases; iii) identify the
information needed by the people affected by rare diseases.
Select forms of communication through which it was possible to supply useful
information to patients, their families and to health workers. It has emerged by analysing
the contents of the focus groups that the needs mostly expressed by the patients and their
families are: i) to make their rights acknowledged by those involved in the subject; ii) to be
heard by health workers and to get information in a comprehensible languafe; iii) to have a
health coordinator who should be able to coordinate the work of different specialists and
workers involved in the care and management of the patient. For the health workers the
main needs are:
– continuous education;
– the possibility to be part of a network with the involvement of general practitioner;
84
– to share experiences and knowledge with professionals belonging to different areas;
– the availability of protocols and guidelines.
Furthermore, the compared analysis of different focus groups has shown some point of
concordance about the need of making the communication between different subjects more
effective with a greater listening attitude.
Phase 2: the indication obtained from the focus groups have allowed the elaboration of
two different questionnaires: one for health workers and one for charities. Both had the goal
of eliciting the needs for continuous education in the fields of rare diseases.
This investigation will obtain useful indicators for the setting up of a process of
continuous education for both health workers and people involved in the work of the
charities. Teaching strategies able to develop communication and relational abilities and
update the technical and scientific knowledge of different subjects will also allow sharing
different experiences for an effective cooperation among colleagues of singles services
(group work) and among workers of different services and charities (working in a network).
Phase 3 and 4: for the following phases we plan the monitoring of the modified aspects
of knowledge and behaviour of those who have taken part in the study through a self
monitoring form. Finally, the data will be collected and analysed. Guidelines will be put in
writing and there will be a proposal of implementation of the project nationwide.
Conclusions. The preliminary results give interesting hints about the needs of people
involved in rare diseases. These elements are necessary in order to achieve all the goals of the
project and could be used for projects about prevention, diagnosis and treatment in a complex
and sensitive area like rare diseases.
85
P. FOLIC ACID EXCESS: HEALTH RISKS EVIDENCE?
Recent concerns for possible adverse effects due to high Folic Acid (FA) intake brought
to a reconsideration of the general FA fortification in food. Such risks, relating to vitamin
B12 metabolism interferences and to cancer promotion, should be characterized from a
qualitative and quantitative point of view. Herewith we discuss the preliminary results of a
work presented to the European Food Safety Authority; we evaluated the available
evidences on the correlation between biomarkers of folate status (folate levels in serum,
plasma or red blood cells) and adverse effects of FA in populations in which generalized
FA flour fortification has been performed. The following indications emerge:
– internal exposure data, beyond being limited, are not easily comparable because
different biomarkers are used as well as units of measurement (eg., ng/ml or nmol/l);
– a narrow population fraction (<5%) over 60 shows a correlation between vitamin
B12 low levels and high folates levels;
– for colorectal cancer there is mainly an indirect evidence of protective effect of low
folate levels;
– a recent study suggests a correlation between folate high levels and an increased risk
for mammary cancer (mainly postmenopausal);
– prostate cancer studies show a risk associated with high vitamin B12 levels, but not
with folates;
– there no indications of a protective role towards colorectal, breast or prostate
tumours by folate high levels (i.e., the higher quintile or quartile of the selected
biomarkers);
– in general, data shows how FA effects should be considered also in relation with
B12, and possibly other micronutrients as well.
Folate levels in serum or in plasma associated with an initial increment of adverse
effects in vulnerable subjects (middle aged or elderly) are in the ≥25 nmol/l range. Since
such levels are reachable in populations in which general food fortifications is being
performed, a precautionary approach is recommended toward such procedure, at least in
anticipation of further studies. On the other hand, in order to prevent neural tube defects it
is advisable to effectively support strategies such as the promotion of a more proper
nutrition and the periconceptional supplementation.
The present paper is performed within the ISS-NIH Project "Neural tube defects and folic acid"-
Working Unit "Risk-to-Benefit Analysis".
86
P. TOWARD THE ESTABLISHMENT
OF A CHEMICALLY-INDUCED MOUSE MODEL
OF HEPATOBLASTOMA
Francesca Maranghi (a), Stefano Lorenzetti (a), Antonella D'Ambrosio (a), Vincenzo
Lagatta (a), Daniele Marcoccia (a), Gabriele Moracci (a), Roberta Tassinari (a), Marco
Salvatore (b), Mara Viganotti (b), Fabrizio Tosto (b), Antonella Romeo (c), Alessandra Di
Masi (d), Antonio Antoccia (d), Sara Nicolai (d), Armando Magrelli (a), Gianluca Azzalin (e),
Rita Devito (f), Agostino Eusepi (g), Antonio Di Virgilio (g), Domenica Taruscio (b),
Giuseppe Macino (e), Caterina Tanzarella (d), Alberto Mantovani (a)
(a) Dipartimento di Sanità Pubblica Veterinaria e Sicurezza Alimentare, Istituto Superiore
di Sanità, Roma
(b) Centro Nazionale Malattie Rare, Istituto Superiore di Sanità, Roma
(c) Dipartimento del Farmaco, Istituto Superiore di Sanità, Roma
(d) Università degli Studi Roma Tre, Roma
(e) Dipartimento di Biotecnologie Cellulari ed Ematologia, Sezione di Genetica
Molecolare, Policlinico Umberto I, Roma
(f) Ospedale Pediatrico Bambino Gesù, IRCCS, Roma
(g) Servizio Biologico e per la Gestione della Sperimentazione Animale, Istituto Superiore
di Sanità, Roma
Hepatoblastoma (HB), the major primary liver malignancy affecting children, especially
below 2 years of age, is a very rare, sporadic cancer that is associated to some risk factors
such as: low birth weight (and the currently increased survival of pre-term neonates), male
gender, and some rare genetic diseases affecting the cell pathways regulating
proliferation/differentiation (Beckwith-Wiedemann syndrome, Familial Adenomatous
Polyposis, Glucose-Storage Diseases).
Exposure to di(2-ethylhexyl)phthalate (DEHP) has been recently suggested as a factor
that may promote HB pathogenesis. DEHP, a plasticizer used to soften PVC, may interact
with several nuclear receptors (PPARs, PXR); besides being a widespread pollutant,
significant exposure to DEHP may occur through medical devices used in maternal
intensive care units, mainly for parenteral nutrition of pre-term neonates.
The main HB molecular marker appear to be the mislocalization of β-catenin, an event
occurring in almost all HB cases and leading to uncontrolled cell proliferation within
hepatocytes. Despite this, genetic mutations within the β-catenin gene has been shown only
in about 40% HB cases.
HB may occur, albeit at low incidence, in mice: mouse HB is especially observed in
aged (≥1 year) animals upon chronic exposure in early adulthood to certain chemicals (i.e.
benzofuran/BF), thus increasing HB incidence.
As in humans, chemically-induced HB shows a higher incidence in male mice.
However, at present, no data do exist on the induction of HB-like alterations in rodents at
early life stages and/or upon intrauterine exposure.
87
The preliminary results of a chemically-induced HB mouse model based on the
exposure to DEHP are shown. A comparison with BF exposure has been also performed.
CD1 mice have been treated with DEHP (25 and 100 mg/kg body weight per day,
corresponding to rodent LOEL of endocrine and liver effects, respectively) and BF (120
mg/kg body weight per day) during pregnancy and up to weaning. The treatment period
covered the full critical window for liver development and differentiation on mice, starting
at Gestational Day (GD) 12 and completed at birth (GD21). Animals were sampled at
weaning (post-natal day/PND 21) and pre-pubertal (PND35) stages.
Preliminary findings indicate that DEHP and BF have similar effects on liver upon
developmental exposure, although DEHP-induced effects are more pronounced. Such effects
include altered fatty acid and glucose metabolism as evidenced by hepatosteatosis and
reduced glycogen storage, as well as by a trend toward intracellular dislocation of β-catenin.
Interestingly, DEHP-exposed mice showed overall signs of intrauterine growth retardation.
This work is performed within the frame of the project "Tackling rare diseases yet lacking
diagnosis and/or prognosis: a pilot project integrating data collection and experimental studies"
supported by a NIH-ISS 2007-2009 grant.
88
CALLOSAL AGENESIS: A BRAIN MALFORMATION
WITH POLYGENIC ORIGIN. IDENTIFICATION
OF CANDIDATE GENES AND LOCI THROUGH
A MULTIDISCIPLINARY APPROACH OF CLINICAL,
CYTOGENETIC AND MOLECULAR STUDIES
OF A LARGE SET OF PATIENT
WITH CORPUS CALLOSUM ANOMALIES
Susan Marelli, Rita Grasso, Clara Bonaglia, Roberto Giorda, Maria Teresa Bassi, Renato
Borgatti
IRCCS Eugenio Medea, Associazione La Nostra Famiglia, Bosisio Parini, Lecco
89
No mutation has been detected in the following genes, until now: AKT3, NRP1, Netrin1
(performed in 25 subjects), ARX (20 subjects), HESX1 (1 subject) and EMX1 (3 subjects).
Conclusions. On the basis of our and other authors' studies we can reasonably conclude
that AKT3 gene is not involved in callosal agenesis. Other investigation are needed to
understand the role of Netrin1, NRP1, HESX1 and EMX1.
90
PROGNOSTIC AND PREDICTIVE MARKERS
IN THYMIC EPITHELIAL TUMOURS (TET):
A TISSUE MICROARRAY (TMA) -
BASED MULTICENTER STUDY
Mirella Marino (a), Libero Lauriola (b), Robert Martucci (a), Amelia Evoli (c), Giorgio
Palestro (d), Roberto Chiarle (d), Daniele Remotti (e), Roberto Pisa (e), Massimo Martelli (f),
Stefano Ascani (g), Francesco Puma (h), Luigi Ruco (i), Erino Rendina (j), Mauro Truini (k),
Gianni Tunesi (l), Antonella Barreca (d), Stefano Sioletic (b), Ilaria Bravi (g), Francesco
Facciolo (m), Sandro Carlini (m), Rossano Lattanzio (n), Marcella Mottolese (a),
Giovannella Palmieri (o), Pierluigi Granone (p), Mauro Antimi (q), Maurizio Lalle (q),
Anna Ceribelli (r), Massimo Rinaldi (s), Giuseppina Chichierchia (a), Salvatore Conti (a),
Enzo Gallo (a), Gerardina Merola (o), Raffaele Perrone Donnorso (a), Mauro Piantelli (n)
(a) Dipartimento di Patologia, IFO, Istituti Fisioterapici Ospitalieri, Istituto Nazionale
Tumori Regina Elena, IRCCS, Roma
(b) Dipartimento di Patologia, Università Cattolica del Sacro Cuore, Roma
(c) Dipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, Roma
(d) Dipartimento di Scienze Biomediche e Oncologia Umana, Università degli Studi,
Torino
(e) Dipartimento di Patologia, Azienda Ospedaliera S. Camillo-Forlanini, Roma
(f) Unità di chirurgia Toracica, Azienda Ospedaliera S. Camillo-Forlanini, Roma
(g) Dipartimento di Patologia, Università degli Studi, Perugia
(h) Unità di chirurgia Toracica, Università degli Studi, Perugia
(i) Dipartimento di Patologia, II Facoltà di Medicina, Ospedale S. Andrea, Università
degli Studi La Sapienza, Roma
(j) Unità di Chirurgia Toracica, II Facoltà di Medicina, Ospedale S. Andrea, Università
degli Studi La Sapienza, Roma
(k) Dipartimento di Patologia, Istituto Nazionale per la Ricerca sul Cancro, IST, Genova
(l) Dipartimento di Patologia, Ospedale Civile di Pampierdarena, Villa Scassi, Genova
(m) Unità di Chirurgia Toracica, IFO, Istituti Fisioterapici Ospitalieri, Istituto Nazionale
Tumori Regina Elena, IRCCS, Roma
(n) Dipartimento di Oncologia e Neuroscienze, Università degli Studi G. D'Annunzio,
Chieti
(o) Dipartimento di Endocrinologia e Oncologia Molecolare e Clinica, Università degli
Studi, Federico II, Napoli
(p) Unità di Chirurgia Toracica, Università Cattolica del Sacro Cuore, Roma
(q) Medicina Oncologica, Ospedale S. Eugenio, Roma
(r) Medicina Oncologica A, IFO, Istituti Fisioterapici Ospitalieri, Istituto Nazionale
Tumori Regina Elena, IRCCS, Roma
(s) Medicina Oncologica B, IFO, Istituti Fisioterapici Ospitalieri, Istituto Nazionale
Tumori Regina Elena, IRCCS, Roma
91
Background. Thymic Epithelial Tumors (TET) constitute both a diagnostic and a
therapeutical challenge, as the traditional clinical staging criteria and the recently developed
diagnostic pathological criteria although relevant do not disclose the biological tumor
potential. Usually benign, some TET behave as malignant tumors, and relapse several times
and/or develop multiple intrathoracic metastases. The rarity of TET prevented from
establishing an effective therapy for malignant cases. The identification at the diagnosis of
tissue-based statistically significant prognostic and predictive factors could allow to set new
therapeutical strategies.
Material and Methods. 210 TET cases occurring between 1996 and 2008 were collected
in different Institutions from the North, Center and South of Italy, based on a long-lasting
collaboration among Pathologists and Clinicians. Paraffin-embedded duplicate sample
cylinders of the tumors, 2 mm in diameter, were punched and included in a multitumor Tissue
Micro Array (TMA). Normal tissues (normal thymus, hyperplastic thymuses and thymi
adjacent to tumors) were also arrayed in TMAs. ErbB family of thyrosine kinase receptors,
cell cycle regulatory protein (p16/p21/p27/Cyclin D1), apoptotic and antiapoptotic factors
(bax, p53/bcl2), marker of proliferation such as KI67, angiogenic factor such as Vascular
Endothelial Growth Factor (VEGF), VEGF receptors (R1, R2, R3), adhesion/signalling
molecules such as E-Cadherin, b-Catenin, Trop-1/Ep-CAM expression was investigated by
immunohistochemistry and related to the available clinical and follow-up data.
Results. The 2004 WHO TET tumor classification was applied; TMA staining data
analysis is in progress. Among the first results obtained, we found that in the ErbB family
receptor, HER2/neu was very rarely and heterogeneously expressed in thymoma/thymic
carcinoma, in cytoplasmic or membranous localization. Along the entire spectrum of TET,
EGFR expression was seen, its hyperexpression being positively correlated with the
increased epithelial cell density occurring along the B1<B2<B3 sequence. VEGF-R2 was
variably expressed in the thymi examined. In most tumors VEGF-R2 was found to be
variably and heterogeneously cytoplasmically-located, the membranous expression being
observed only in a tumor subset. Trop-1/Ep-CAM staining was observed cytoplasmically
located along the entire spectrum of TET, and strongly expressed on the cell membrane in
some cases.
Conclusions. From these very preliminary data, in addition to EGF-R, we have
identified two possible targets of therapeutic interventions: Trop-1/Ep-CAM (humanized
antibodies) and VEGF-R2 (small TK-inhibitors). The TMA-based approach could
constitute a useful tool to identify in TET "a molecular signature" with significant
prognostic/predictive value.
92
A MULTIDISCIPLINARY APPROACH
FOR THE INVESTIGATION
OF HYPERPARATHYROIDISM-JAW
TUMOUR SYNDROME
Giulia Masi (a), Luisa Barzon (a), Maurizio Iacobone (b), Giovanni Viel (b), Andrea
Porzionato (c), Veronica Macchi (c), Raffaele De Caro (b), Gennaro Favia (b), Giorgio Palù (a)
(a) Dipartimento di Istologia, Microbiologia e Biotecnologie Mediche, Università degli
Studi, Padova
(b) Dipartimento di Scienze Chirurgiche e Gastroenterologiche, Università degli Studi,
Padova
(c) Dipartimento di Anatomia e Fisiologia Umana, Università degli Studi, Padova
HRPT2 germline mutations are responsible for more than half of cases of
Hyperparathyroidism-Jaw Tumor syndrome (HPT-JT) and for a subset of Familial
Isolated Hyperparathyroidism (FIHP). In addition, HRPT2 mutations have been
identified also in sporadic parathyroid carcinomas (67-100%) and, very rarely, in
adenomas (0-4%). The protein encoded by HRPT2 is named parafibromin, and its
expression is impaired in parathyroid tumors from subjects affected by HPT-JT and in
sporadic parathyroid carcinomas.
The first part of our project focused on a clinical, genetic, and histopathologic
study in three unrelated Italian kindreds with HPT-JT and FIHP. HPT-JT and FIHP
patients had similar laboratory, clinical, and demographic features and shared
primary hyperparathyroidism and other neoplasms, the most common of which was
uterine polyposis.
The kindreds had also the same genetic background, characterized by the occurrence of
inactivating mutations of the HRPT2 gene: in fact, we identified, by direct sequencing of
the entire coding region and the intron-exon boundaries of the HRPT2 gene, germline
mutations in the probands and in all affected patients of the three kindreds.
Genetic analysis of tumor samples demonstrated a second somatic HRPT2 mutation
only in a parathyroid adenoma and no cases with loss of the wild-type allele or methylation
of the HRPT2 promoter, even though immunohistochemical analysis demonstrated loss of
nuclear parafibromin expression in all tumors, including a uterine polyp.
Our study also demonstrated hyperparathyroidism in FIHP patients with HRPT2
mutations is often characterized by single-gland involvement, and in most cases a limited
parathyroidectomy achieved a long-term cure.
Moreover, we are also collecting a large series of sporadic parathyroid tumors,
comprising to date 45 adenomas and 3 carcinomas. We performed direct DNA sequencing
of the complete HRPT2 coding region in the three carcinomas and we detected a somatic
heterozygous nonsense mutations only in a case of parathyroid carcinoma occurring in a
young woman that previously underwent surgery for the excision of a jaw tumor. We also
demonstrated the absence of nuclear anti-parafibromin immunoreactivity in the parathyroid
tumor, but intense immunostaining was present in the jaw tumor.
93
Finally, we are currently analyzing parafibromin expression by western blotting in our
series of sporadic parathyroid tumors; our preliminary results indicate that there are no
substantial differences in parafibromin expression among different parathyroid adenomas; a
correlation with HRPT2 mRNA expression and parafibomin immunohistochemistry is in
progress.
94
USEFULNESS OF MLPA IN THE MOLECULAR
DIAGNOSIS OF LISSENCEPHAY AND NEURONAL
MIGRATION DISORDERS
Davide Mei, Elena Parrini, Simone Gana, Carla Marini, Renzo Guerrini
Sezione e Laboratorio di Neurologia e Neurogenetica Pediatrica, Ospedale Pediatrico A.
Meyer, Università degli Studi, Firenze
95
DIAGNOSTIC AND THERAPEUTIC TARGET
OF SYSTEMIC AMYLOIDOSIS:
VALIDATION OF NEW DIAGNOSTIC TOOLS
AND DEVELOPMENT OF NEW DISEASE MODELS
Giampaolo Merlini (a,b), Laura Obici (a), Giovanni Palladini (a), Francesca Lavatelli (a),
Mario Nuvolone (a), Simona Donadei (a), Sofia Giorgetti (b), Palma Mangione (b), Sara
Raimondi (b), Monica Stoppini (b), Vittorio Bellotti (a,b)
(a) Centro per lo Studio e la Cura delle Amiloidosi Sistemiche, Fondazione IRCCS
Policlinico San Matteo, Pavia
(b) Dipartimento di Biochimica, Università degli Studi, Pavia
New diagnostic and therapeutic strategies for systemic amyloidoses can be based on
detailed information on composition of natural fibrils and structural/functional
characterisation of tissue-specific molecular interactors locally active on amyloid
deposition. We have developed a proteomic approach in order to identify the pathogenic
protein in the biopsy of the abdominal fat, which is the tissue of choice for the diagnosis of
systemic amyloidosis. This represents a novel powerful diagnostic tool for assessing
unequivocally the type of amyloidosis.
We are also investigating the physiologic proteomic pattern of subcutaneous adipose
tissue. The definition of proteins expressed in non-pathological tissue allows identifying
enzymes and proteins that play key roles in metabolic pathways potentially affected by the
amyloid deposition.
Results provided by the proteomic approach have been exploited in the assessment of
new methods of fibrillogenesis of globular proteins that mimic the natural environment. In
particular through the combination of collagen, collagen plus heparin and minimal amount
of truncated β2-microglobulin we can now grow amyloid fibrils at neutral pH.
In particular, we have demonstrated that homogenous heparin at concentration of 1-3
μg/ml, consistent with concentration occurring in vivo during haemodialysis, strongly
favours amyloid formation.
Our data suggest that heparin would favour fibrillogenesis by catalyzing the generation
of soluble oligomers correctly oriented in a cross-beta structure.
The mechanism of early aggregation is under extensive investigation and we have
discovered that certain strands of β2-microglobulin have a prominent role in the early
phases of oligomerization.
The multiple methods of fibrillogenesis, whose dynamics can be now monitored at the
molecular level, allow investigating the properties of new and old drugs able to prevent
protein fibrillogenesis.
Extremely promising results have been obtained through a collaborative work with
Mario Negri Institute in Milan which is providing new analogues of tetracyclines and other
heterocyclic small molecules that in vitro display significant anti-amyloidogenic property.
Furthermore, we have investigated the development of amyloid deposits, constituted by the
lipoprotein ApoA-II, in the aging CD1 mouse strain.
96
We have found that the amyloid is deposited in spleen and liver, but also in the heart, an
organ that is rarely involved in other amyloid mice models. The amyloid deposition in the
heart is now under extensive investigation in order to correlate the molecular abnormalities
and the histo-pathological features with the echocardiographic and MRI patterns.
97
GENETIC ABNORMALITIES OF COMPLEMENT
MOLECULES IN HEMOLYTIC UREMIC SYNDROME
Chiara Mossali (a), Gaia Pianetti (a), Federica Castelletti (a), Jessica Caprioli (a), Elena
Bresin (a), Giuseppe Remuzzi (a,b), Marina Noris (a)
(a) Centro di Ricerca sui Trapianti Chiara Cucchi de Alessandri e Gilberto Crespi, Istituto
di Ricerche Farmacologiche Mario Negri, Bergamo
(b) Dipartimento di Nefrologia e Dialisi, Ospedali Riuniti, Bergamo
98
P. EVALUATION OF GENETIC AND ENVIRONMENTAL
FACTORS IN A COHORT OF TWINS
WITH AMYOTROPHIC LATERAL SCLEROSIS (ALS)
Lorenza Nisticò (a), Rodolfo Cotichini (a), Maria Rosaria Monsurrò (b), Leandro
Provinciali (c), Antonino Uncini (d), Dario Benincasa (e), Francesco Pontieri (e), Giovanni
Lagalla (c), Margherita Capasso (d), Ettore Beghi (f), Francesca Trojsi (b), Letizia Mazzini (g),
Adriano Chiò (h), Elena Giacomelli (i), Stefano Zoccolella (j), Vittorio Govoni (k),
Rossella Spataro (l), Vincenzo La Bella (l), Giovanni Antonini (e), Ilaria Casetta (k),
Maurizio Inghilleri (i), Jessica Mandrioli (m), Elisabetta Bucci (e), Gianni Sorarù (n),
Andrea Millul (f), Paolo Bongioanni (o), Valentina Cima (n), Giancarlo Logroscino(j),
Patrizia Sola (m), Nicola Nasuelli (g), Bruno Rossi (o), Nicola Vanacore (a), Virgilia
Toccaceli (a), Maurizio Leone (g)
(a) Centro Nazionale di Epidemiologia, Sorveglianza e Promozione della Salute, Istituto
Superiore di Sanità, Roma
(b) II Divisione Neurologia, Seconda Università degli Studi, Napoli
(c) Clinica Neurologica, AO Universitaria Ospedali Riuniti, Ancona
(d) Clinica Neurologica, Università degli Studi G. d'Annunzio, Chieti
(e) Dipartimento di Neuroscienze, Ospedale S. Andrea, Università degli Studi La Sapienza,
Roma
(f) Dipartimento di Neuroscienze, Istituto di Ricerche Farmacologiche Mario Negri,
Milano
(g) Reparto di Neurologia, AO Universitaria Maggiore della Carità, Novara
(h) Dipartimento Neuroscienze, Università degli Studi, Torino
(i) Dipartimento di Scienze Neurologiche, Policlinico Umberto I, Università degli Studi La
Sapienza, Roma
(j) Dipartimento di Scienze Neurologiche e Psichiatriche, Policlinico Università degli
Studi, Bari
(k) Clinica Neurologica, Azienda Ospedaliera, Università degli Studi, Palermo
(l) Clinica Neurologica, Nuovo Ospedale Civile S. Agostino Estense, Modena
(m) Dipartimento di Neuroscienze, Università degli Studi, Padova
(n) Dipartimento di Neuroscienze, Università degli Studi, Pisa
99
Twenty-two ALS twins (15 males) are from same sex pairs and 7 (6 male) belong to
unlike sex pairs. As regards living status, in 1 pair both twins (ALS twin and co-twin) are
deceased, while in 15 pairs 14 ALS twins and 1 co-twin are deceased. Health status or
cause of death of co-twins will be ascertained by a neurologist.
Life exposure to putative ALS risk factors will be investigated through a co-twin control
study. Collection of biological material from ALS and unaffected twins is also envisaged.
100
CHARACTERIZATION OF THE MOLECULAR
AND CELLULAR MECHANISMS
UNDERLYING THE LIVER PATHOGENESIS
IN HEMOPHAGOCYTIC SYNDROMES (HS)
Luigi Notarangelo (a), Angela Santoni (b), Silvano Sozzani (c), Antonio Sica (d)
(a) Dipartimento di Pediatria, Spedali Civili, Università degli Studi, Brescia
(b) Dipartimento di Medicina Sperimentale, Università degli Studi La Sapienza, Roma
(c) Sezione di Patologia Generale ed Immunologia, Dipartimento di Scienze Biomediche e
Biotecnologiche, Università degli Studi, Brescia
(d) Humanitas Mirasole SpA, Istituto Clinico Humanitas, IRCCS, Rozzano, Milano
Hemophagocytic Syndrome (HS) is a severe and often fatal syndrome resulting from
potent and uncontrolled activation and proliferation of T lymphocytes, leading to excessive
macrophage activation and multiple deleterious effects. This project is devoted to a better
characterization of the mechanisms underlying the liver pathology of the HS. Our preliminary
results indicate at least two new mechanisms potentially involved in HS progression.
We have characterized the role of chemerin, the ligand of the chemotactic receptor
ChemR23, in inducing the recruitment and co-localization of Myeloid Dendritic Cells (M-
DC), Plasmacytoid DC (P-DC) and NK cells. The three cell types express high levels of
functional ChemR23 and chemerin is highly expressed in the liver. Chemerin expression
was not found in these leukocyte populations in none of the conditions investigated. To
gain insight in the cell type responsible for chemerin production in the liver we decided to
use in situ hybridisation. To this goal a specific probe was cloned in pBSKS+ vector and
sections from human liver and lymph nodes, these experiments are still ongoing. Finally,
chemerin did not stimulate NK cell in vitro, cytokine production, NK cell degranulation
and killing of K562 cells. We propose that chemerin, in addition to certain chemokines
known to be produced by activated Kupffer cells, such as CCL20, may induce the
colocalization of innate immunity effector cells in pathological conditions, such as HS.
9 patients with clinical manifestations resembling HLH were classified according to
current diagnostic criteria of Hystiocyte Societ. Patients presented the following clinical
manifestations were as follows: fever was observed in 100% of patients, splenomegaly
100% of subjects, single lineage cytopenia (anemia, thrombocytopenia or neutropenia)
88%, hemophagocytosis (78%), Impaired NK cell cytotoxicity (100%).
Genetic analysis of PRF1 and UNC13D was performed in all subjects. Three of them
displayed mutations of PRF1, while another one carried UNC13D mutation. We have
analyzed NK and NK-T cells in two patients affected by Hermansky-Pudlak type 2.
Preliminary data suggest abnormal distribution of NK cell subset and complete absence of
NK-T cells. In these subjects, analysis of CD63 expression on cell surface has shown
increased levels on cell surface. Moreover, CD63 expression is not regulated after
activation, suggesting that CD63 transport to plasmamembrane is altered in these subjects.
101
P. ALTERNATIVE SPLICING, CAN BE A MARKER
OF UVEAL MELANOMA
Paola Orecchia (a), Romana Conte (a), Valentina Rea (a), Claudia Manzini (b), Ulrich
Pfeffer (a), Gabriella Pietra (a,b), M. Cristina Mingari (a,b), Barbara Carnemolla (a)
(a) Istituto Nazionale per la Ricerca sul Cancro, IST, Genova
(b) Dipartimento di Medicina Sperimentale, Università degli Studi, Genova
Cancer cells can alter their adjacent stroma to form a permissive and supportive
environment for tumor progression and produce a range of growth factors and proteases
that modify their stromal environment. These factors disrupt normal tissue homeostasis and
act in a paracrine manner to induce angiogenesis, inflammation, as well as activation of
surrounding stromal cell types.
The induction of inflammation in the tumour stroma also results in production of a
range of factors including Extra Cellular Matrix (ECM) components that promote tumour
progression. Periostin is a secretory omodimeric protein of the ECM with an apparent
molecular mass of 180 kDa, involved in cell adhesion and tumor formation that is produced
in the stromal environment.
Recently, it has been reported that the periostin expression levels increase in primary
and metastatic melanoma due to both stromal and tumoral cells production. Although
splicing variants of periostin have been described in bladder cancer tissues, to date nothing
is known on periostin isoforms expression in melanoma.
To study periostin isoforms as new potential tumoral markers, we analyzed the
alternative splicing of the human periostin transcript in tumoral cells and fibroblasts
isolated from cutaneous metastatic melanoma tissues. Preliminary results indicate that both
types of tumor-derived cells produce periostin mRNA, but only melanoma cells express
exon 17 in 50% of cases (3/6).
On the contrary, all (4/4) the uveal melanoma tissues analyzed so far express isoforms
of periostin containing the exon 17, thus suggesting that exon 17 of human periostin can be
a potential marker of this tumor.
102
QUALITY OF LIFE AND DISABILITY
IN FABRY DISEASE
Costanza Pazzaglia (a), Pietro Caliandro (a,b), Matteo Russo (c), Andrea Frustaci (d),
Claudio Feliciani (e), Luca Padua (a,b)
(a) Istituto di Neurologia, Università Cattolica del Sacro Cuore, Roma
(b) Centro S. Maria della Pace, Fondazione Don C. Gnocchi Onlus, Roma
(c) Dipartimento di Medicina e Patologia Sperimentale, Università degli Studi La
Sapienza, Roma
(d) Dipartimento di Cardiologia e Chirurgia Vascolare, Università degli Studi La
Sapienza, Roma
(e) Dipartimento di Dermatologia, Università Cattolica del Sacro Cuore, Roma
103
TARGETING THE PROGNOSTIC AND METASTASIS-
PREDICTING SURFACE PROTEOGLYCAN
FOR IMMUNOTHERAPEUTIC TREATMENT
OF SELECTED SARCOMAS
Roberto Perris (a,b), Sabrina Cattaruzza (b), Pier Andre Nicolosi (b), Maria Teresa
Mucignat (b), Katia Lacrima (a), Nicoletta Bertani (a), Laura Pazzaglia (c), Maria Serena
Benassi (c), Lucia Sigalotti (d), M. Guidoboni (d), Michele Maio (d), W.B. Stallcup (e),
Piero Picci (c)
(a) Dipartimento di Genetica e Microbiologia Antropologica, Università degli Studi,
Parma
(b) Divisione Sperimentale Oncologica 2, Centro di Riferimento Oncologico, IRCCS,
Aviano, Pordenone
(c) Istituti Ortopedici Rizzoli, Bologna
(d) Dipartimento di Oncologia, Università degli Studi, Siena
(e) The Burnham Institute for Molecular Biology, La Jolla CA, USA
A recent analysis of the transcriptional and protein expression profile in primite and
metastatic lesions of more than 70 soft-tissue sarcoma patients reveals an unprecedented
role for the cell surface proteoglycan NG2 in predicting with more than 50% probability
future, post-operative metastatic disease.
This finding, taken together with the lower survival rates of patients with enhanced
NG2 expression, assigns to the proteoglycan a value as independent prognostic factor and
has incited a multicenter extension of the investigations, with particular emphasis on
relapsing frequences and therapeutic responses. In parallel efforts, by employing more than
30 sarcoma lines established from surgical specimens, in vitro growth, adhesion and cell
migration assays and transplantation into wild type and transgenic mice, we have resolved
some of the cellular and molecular mechanisms underlying the modes through NG2 may
promote tumour growth and metastasis formation. DNA microarray-based gene profiling
and combined proteomic and phosho-proteomic profiling was employed to delineate the
gene and signalling networks associated with the NG2 pro-tumorigenic role. The
acquisition of this background information has provided a significant support for the
immunotherapeutic targeting of the proteoglycan in soft-tissue sarcoma patients, based upo
the exploitation of anti-NG2 anti-idiotypic approaches (and agents) recently proven to be
effective on advanced melanoma patients.
To this end we have specifcally examined some of the immunological traits of antibody
MK23-3 found to be able to induce T cell responses cross-reacting with NG2 and
discovered to behave as an "heteroclitic vaccine". Combined bioinformatic analyses and in
vitro assays on T lymphocytes suggest that this ability of anti-idiotypic antibody to induce
the observed immune responses may be explained, at least in part, by the homology of
variable heavy chain of this antibody with short 10-17 amino acid stretches of NG2.
104
These elaborations have set the ground for also identify particularly immunogenic
peptide sequences that could be used in conjunction with anti-idiotypic antibodies, also in
non-responders.
In a separate experimental series aimed at generating immunological therapeutic
reagents to be trasfereed to clinical settings on soft-tissue sarcoma patients we have
produced a panel of 63 anti-NG2 monoclonal antibodies. A first characterization of these
antibodies have yielded unexpected variations in the ability of the antibodies to recognize
the antigen on diverse soft-tissue sarcoma cells suggesting a structural-functional diversity
of the proteoglycan.
Functional analyses are in progress to address the tumorigenic significance of these
variations and potential utility of these reagents as tumour abrogating agents in vivo.
105
P. EVIDENCES FOR ASSOCIATION
OF THE CASP8-652 6N DEL PROMOTER
POLYMORPHISM WITH AGE AT DIAGNOSIS
IN FAMILIAL BREAST CANCER CASES
Paolo Peterlongo (a,b), Giovanna De Vecchi (a,b), Paolo Verderio (c), Sara Pizzamiglio (c),
Siranoush Manoukian (d), Monica Barile (e), Stefano Fortuzzi (f), Fernando Ravagnani (g),
Marco A. Pierotti (h), Paolo Radice (a,b)
(a) Fondazione Istituto di Oncologia Molecolare, IFOM, Fondazione Italiana per la
Ricerca sul Cancro, FIRC, Milano
(b) Unità di Suscettibilità Genetica al Tumore, Dipartimento di Oncologia Sperimentale,
Fondazione IRCCS, Istituto Nazionale dei Tumori, Milano
(c) Unità di Statistica e Biometria Medica, Fondazione IRCCS, Istituto Nazionale dei
Tumori, Milano
(d) Unità di Genetica Medica, Dipartimento di Oncologia Sperimentale, Fondazione
IRCCS, Istituto Nazionale dei Tumori, Milano
(e) Divisione di Prevenzione dei Tumori e Genetica, Istituto Europeo di Oncologia, IEO,
Milano
(f) Consortium for Genomic Technologies, Cogentech, Milano
(g) Servizio di Medicina Immunoematologica e Trasfusionale, Fondazione IRCCS, Istituto
Nazionale dei Tumori, Milano
(h) Fondazione IRCCS, Istituto Nazionale dei Tumori, Milano
106
analyses and investigated the association between the polymorphism and age at BC
diagnosis in cases. The three genotypes were collapsed into two: (del/del), and (nor/-) by
aggregating common homozygous and heterozygous cases; the age at diagnosis was
categorized into four classes according to the pertinent age centiles (25th: 35; 50th: 43; 75th:
50). We assessed the associations between each age class and genotype by the logistic
regression model and observed a statistically significant association between these two
variables. In particular, our results suggested an increasing trend of the del/del genotype
with later age at BC diagnosis (trend test p-value=0.01).
Conclusion. We observed that the -652 6N del polymorphism of CASP8 was associated
with age at diagnosis in familial BC cases. Thus, we suggest that this polymorphism may
have an effect in postponing the BC onset in predisposed individuals.
107
ROLE OF THE DYSTROPHIN-ASSOCIATED
GLYCOPROTEIN COMPLEX IN LIMB-GIRDLE
AND CONGENITAL MUSCULAR DYSTROPHIES:
FROM MOLECULAR PATHOPHYSIOLOGY
TO POTENTIAL THERAPY (7DR1)
Tamara C. Petrucci (a), Enzo Ricci (b), Andrea Brancaccio (c), Pompeo Macioce (a),
Marina Ceccarini (a)
(a) Dipartimento di Biologia Cellulare e Neuroscienze, Istituto Superiore di Sanità, Roma
(b) Istituto di Neurologia, Università Cattolica del Sacro Cuore, Roma
(c) Istituto di Biochimica e Biochimica Clinica, Consiglio Nazionale delle Ricerche;
Università Cattolica del Sacro Cuore, Roma
The aim of our project, which involves four groups, is to improve our understanding of
the underlying mechanisms that produce a dystrophic phenotype, focusing our studies on
the components of the Dystrophin-associated Glycoprotein Complex (DGC), that is
dystrophin, the dystroglycans (α and β), the sarcoglycans (α, β, γ and δ), sarcospan, the
syntrophins (α1, β1and β2) and α-dystrobrevin. We focused our studies on: i) the analysis
of muscle tissue gene expression profile in cases of Congenital Muscular Dystrophies
(CMD) due to merosin deficiency or associated with α-DG hypoglycosylation; ii) the role
of dystroglycan in cell adhesion and cell signalling; iii) the emerging functions of
dystrobrevin as motor adaptor and signalling scaffold protein.
We (UO2, Ricci-Brancaccio) have analyzed the dystroglycan α/β interface, in order to
better characterise the reciprocal intersubunit binding sites. We have identified four amino
acids that are crucial for the interaction between the two subunits and found that their
substitution with Ala residues in transfected Ebna-293 cells altered the DG processing,
preventing the cleavage that separates α-DG and β-DG. A group of patients affected by
different types of muscular dystrophies have been analysed in order to assess the possible
contribution of the DG α/β interface to the pathology of skeletal muscle. In addition,
characterization of muscle biopsies of patients with a known diagnosis of CMD has been
performed using oligonucleotide microarrays technology, genetic analysis and
immunohistochemistry Cognitive impairment and mental retardation are often associated
with muscle atrophy in some congenital forms of muscular dystrophies, as the laminin α2-
deficient CMDs.
We (UO1, Petrucci) used the C57BL dy2J/dy2J mouse, an animal model of α2-deficient
CMD, and littermate controls, to analyse by western blot and immunohistochemistry the level
of DGC components both in skeletal muscle and brain extracts. We found that dystroglycan
processing was altered in both tissues, and syntrophin was upregulated in skeletal muscle of
dy2J/dy2J compared to control mice. The cytoplamic components of the DGC, syntrophin and
dystrobrevin are known to be involved in signal transduction and DGC stabilization. We
(UO4, Ceccarini) have characterized the interaction between β-dystrobrevin and the
molecular motor kinesin, and hypothesized that this interaction could be functional to the
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intracellular transport of dystrobrevin and its binding partners, including PKA regulatory
subunits and dysbindin, a component of the Biogenesis of Lysosome-related Organelles
Complex 1 (BLOC-1) that regulates synthesis and trafficking of lysosome-related organelle.
We found that both PKA-dependent phosphorylation of dystrobrevin and the presence of Ca++
can significantly lower the binding affinity of dystrobrevin-kinesin interaction, whereas
dystrobrevin-dysbindin interaction was unaffected.
Among the new dystrobrevin interacting protein we have identified (UO3, Macioce)
iBRAF/HMG20a, a member of the HMG-proteins that modulate chromatin structure. We
have characterized β-dystrobrevin interaction with iBRAF by in vitro and in vivo assays,
and obtained results that suggest β-dystrobrevin, through its association with iBRAF, may
be involved in regulating chromatin dynamics and consequently play a role in the activation
of neuronal specific genes.
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ESTABLISHMENT OF A EUROPEAN NETWORK
OF RARE BLEEDING DISORDERS (RBDS)
Flora Peyvandi (a), Marta Spreafico (b), Marzia Menegatti (c), Roberta Palla (a), Angiola
Rocino (b), Alfonso Iorio (b), Pier Mannuccio Mannucci (a,b)
(a) Dipartimento di Medicina e Specialità Mediche, Fondazione IRCCS, Ospedale
Maggiore Policlinico Mangiagalli e Regina Elena, Milano
(b) Associazione Italiana Centri Emofilia, AICE, Milano
The aim of the project is to set up a network of Italian and other European Centres
dealing with patients affected by RBDs in order to implement the already existing RBDD
database (www.rbdd.org).
The main partner, at present the only Italian participating centre, involved other
European Centres in the testing phase of the database meant to optimize its on-line
functions, verifying the proper setting of the help, controls on guided choices, clarity of
field-browsing, simplicity of interrogation tools. Partners were able to access the database
through activation of an account and a protected certification. After an initial data input,
partners cited anomalies, logical, browsing and comprehension errors, possible
improvements or modification proposals. The changes considered fundamental for the
correct working of the database will be made, but only after an agreement has been reached
within the network.
Moreover, Associazione Italiana Centri Emofilia (AICE), a reliable association
regarding treatment Centre coordination and patients assistance in the field of hemophilia,
was involved to create an Italian National Registry on RBDs, similar to that created by us at
European level. This collaboration was aimed to link the information on RBDs patients
inserted in the Emocard, the AICE computer-based clinical data collection system, with
those inserted in the European and RBDD databases. To understand whether the two
databases could communicate and collect data homogenously, a comparison of the
respective fields was carried out, showing that the two databases are similar, because the
majority of information requested by RBDD are already contained in Emocard. However,
few important fields (e.g. parents' consanguinity, antigen level, bleeding score) present in
the RBDD questionnaire are not foreseen in Emocard. To uniform the two data collection
forms, additional pages will be added to the Emocard questionnaire. Emocard information
on RBDs patients will be periodically extracted and sent to Flora Pevyandi, responsible of
the European project, who will try to improve the harmonization of data collection, analysis
and extraction of those data which will be necessary to draw therapeutic guidelines. This
will lead us to avoid duplication of data insertion.
In conclusion, it is desirable that within next year, all Italian Centres affiliated to AICE
will adhere to this project with the aim of creating a National Registry, not yet available.
Data collected in the Italian cohort will implement the already large European cohort, thus
allowing to draw adequate statistical analysis, useful to clinical practice, by organization of
therapeutic guidelines.
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BIOCHEMICAL AND CELLULAR
REAL-TIME BIOMARKERS OF DIAGNOSTIC
AND PROGNOSTIC VALUE IN THE MANAGEMENT
OF KAWASAKI'S DISEASE
Donatella Pietraforte (a), Elisabetta Straface (b), Alessio Metere (a), Lucrezia Gambardella (b),
Luciana Giordani (b), Elisabetta Cortis (c), Alberto Villani (c), Domenico Del Principe (d),
Marina Viora (b), Maurizio Minetti (a), Walter Malorni (b)
(a) Dipartimento di Biologia Cellulare e Neuroscienze, Istituto Superiore di Sanità, Roma
(b) Dipartimento del Farmaco, Istituto Superiore di Sanità, Roma
(c) Ospedale Pediatrico Bambino Gesù, IRCCS, Roma
(d) Università degli Studi Tor Vergata, Roma
Two different points have been analyzed as valuable biomarkers of diagnosis and
progression in blood samples from patients with Kawasaki Disease (KD): oxidative stress
and blood cell integrity and function.
Background. Persistent arterial dysfunction in patients with a history of KD and an
integral role of oxidative stress in the development of cardiovascular disease are
increasingly recognized. We sought to test the hypothesis that oxidative stress is increased
in KD patients by evaluating different possible plasmatic and cellular biomarkers. In
addition, platelets are increased in their number in KD and their alterations have been
suggested to exert a pathogenetic role.
Methods. We measured by Electron Paramagnetic Resonance spin trapping with 1-
hydroxy-3-carboxy-2,2,5,5-tetramethylpirrolydine (CPH) the production of free radicals in
whole blood of KD patients compared to control health subjects.
As concerns blood cells, erythrocytes and platelets were analyzed by static and flow
cytometry. Regarding erythrocytes, redox imbalance and expression of proteins
(glycophorin A and CD47) involved in cell aging and death were evaluated. Regarding
platelets, in order to mimic the clinical situation, an immunologic stimulus has been used
(opsonized zymosan) and their aggregation and adhesion features as well as their death
susceptibility have been analyzed.
Results. Compared with controls, patients with KD had significantly higher rate of free
radical production as demonstrated by the increase (+86% p<0.001) of the rate of CP•
radical formation. The rate of CP• formation further increased about 4-5 times after
addition of the transition-metal chelator EDTA, leading to the hypothesis that the increased
radical formation may be mediated by catalytically active Iron. After therapy (aspirin
2mg/Kg/die) the rate of CP• formation was decreased, but still significantly higher than
controls (+30% p<0.001). As concerns erythrocytes, a decreased expression of glycophorin
A and CD47 has been detected in KD patients with respect to healthy donors.
For platelets, main finding deals with their increased aggregability and, more
importantly, the increased Phosphatydilserine (PS) externalization without further sign of
cell death (e.g. no caspase activation).
111
Conclusions. Our findings suggest: i) oxidative stress is increased in KD patients at the
onset of the disease. We suggest the presence of an inflammatory condition perhaps
mediated by Iron overload and/or decompartmentalization; ii) the increased platelet counts
in these patients could be due to a defective death pathway whereas PS externalization
could be associated with an increased vascular risk. Altogether these findings suggest that
further studies should be performed in KD blood samples in order to better assess these
hypotheses that could help in the clinical management of this disease.
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IMPAIRED CORTICOSTRIATAL LTD
AND SYNAPTIC DEPOTENTIATION IN A MODEL
OF DYT1 DYSTONIA DEPENDS ON DYSREGULATED
CHOLINERGIC SIGNALING
Antonio Pisani (a), Giuseppe Sciamanna (a), Paola Bonsi (a), Giuseppina Martella (a),
Dario Cuomo (a), Paola Platania (a), A. Tassone (a), Patrizia Popoli (b), Giorgio Bernardi (a)
(a) Fondazione Santa Lucia, IRCCS; Dipartimento di Neuroscienze, Università degli Studi
Tor Vergata, Roma
(b) Dipartimento del Farmaco, Istituto Superiore di Sanità, Roma
Clinically unaffected DYT1 gene carriers exhibit subtle abnormalities in motor behavior
with impaired sequence learning. Corticostriatal synaptic plasticity is believed to play a
central role in motor learning. We investigated possible changes in synaptic plasticity in
transgenic mice expressing either the human Wild-type TorsinA (hWT) or Mutant TorsinA
(hMT). High-Frequency Stimulation (HFS) induced Long-Term Depression (LTD) in
MSNs recorded from control and hWT mice, but failed to cause LTD in hMT littermates.
Pretreatment with D1 or D2 dopamine receptor agonists was unable to restore LTD,
whereas combined application of both agonists partially rescued LTD. Because a
paradoxical, excitatory D2-dependent effect has been shown in cholinergic interneurons
from hMT mice, we tested the possibility that an excess in Acetylcholine (ACh) striatal
levels could impair LTD.
Pre-incubation with either hemicholinium, which depletes endogenous ACh, or with the
M1-preferring ACh-muscarinic receptor antagonists, pirenzepine and trihexyphenidyl,
restored LTD. In the absence of magnesium, HFS was able to induce a Long-Term
Potentiation (LTP) in MSNs recorded from either controls or hWT mice. In hMT mice the
magnitude of LTP was significantly higher than in hWT and controls. Once obtained a
stable LTP, a Low-Frequency Stimulation (LFS) protocol was able to induce a Synaptic
Depotentiation (SD) both in controls and hWT mice.
However, LFS failed to determine SD in hMT mice. Similarly to what observed for
LTD, both hemicholinium and pirenzepine rescued SD when applied after LTP induction.
Likewise, in mice deficient for the muscarinic autoreceptor M4, we did not observe SD.
Together, these results suggest that a dysregulation in the dopaminergic control over
cholinergic signaling impairs synaptic plasticity in the striatum of DYT1 transgenic mice.
These functional alterations might represent the cellular bases for the motor abnormalities
observed in non-manifesting DYT1 carriers.
113
RELIABILITY AND EFFICACY OF THE CURRENT
DIAGNOSTIC APPROACH IN NARCOLEPSY
AND SEARCH FOR NEW GENETIC MARKERS
Giuseppe Plazzi (a), Christian Franceschini (a), Filomena I.I. Cosentino (b), Paolo Bosco (c),
Luigi Ferini Strambi (d), Sara Marelli (d), Oliviero Bruni (e), Raffaele Ferri (b)
(a) Dipartimento di Scienze Neurologiche, Università degli Studi, Bologna
(b) Centro di Medicina del Sonno, Dipartimento di Neurologia, Troina, Enna
(c) Laboratorio di Citogenetica, IRCCS Associazione Oasi di Maria SS., Troina, Enna
(d) Centro di Medicina del Sonno, Dipartimento di Neurologia, Università Vita-Salute San
Raffaele, Fondazione San Raffaele del Monte Tabor, IRCCS, Milano
(e) Centro di Medicina del Sonno, Dipartimento di Neurologia e Psichiatria dello Sviluppo,
Università degli Studi La Sapienza, Roma
114
characterizing narcolepsy was the occurrence of a REM sleep period at sleep onset
(SOREMP). Moreover, the night sleep was characterized by reduced sleep efficiency
(84.5±32.44%) - due to fragmented sleep for repeated nocturnal awakenings - and by the
presence of PLMS (PLM index 14.9±22.5). All patients showed, on average, a significant
increase of BMI (28.0±4.69).
Discussion. Our study confirms that narcolepsy is a complex sleep disorder characterized
by several clinical daytime symptoms and nocturnal sleep disorders. It also suggests that the
sleep/wake cycle dysregulation may be linked to an alteration of the hypothalamic
hypocretin's system.
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INCIDENCE OF "CHROMOSOMAL PHENOTYPE"
IN MENTALLY RETARDED CARRIERS
OF PATHOGENIC COPY NUMBER
VARIATIONS (CNVS)
Corrado Romano (a), Francesco Calì (b), Santina Reitano (a), Donatella Greco (a), Pinella
Failla (a), Valeria Chiavetta (b), Pietro Schinocca (b), Ornella Galesi (c), Daniela Di
Benedetto (c), Lucia Castiglia (c), Roberto Ciccone (d), Orsetta Zuffardi (d), Marco Fichera (c)
(a) Unità Operativa Complessa di Pediatria e Genetica Medica, IRCCS Associazione Oasi
di Maria SS., Troina, Enna
(b) Laboratorio di Genetica Molecolare, IRCCS Associazione Oasi di Maria SS., Troina,
Enna
(c) Laboratorio di Diagnosi Genetica, IRCCS Associazione Oasi di Maria SS., Troina,
Enna
(d) Genetica Medica, Università degli Studi, Pavia
Array CGH assays showed CNVs in patients with mental retardation, resulted normal to
routine cytogenetic analysis, in a percentage of 5-25% depending on techniques used and
selection patients method. Frequently, the candidates to array-CGH analysis are patients
with "chromosomal phenotype".
The aims of our project "Usefulness of 244K array-CGH in the ascertainment of Cryptic
Chromosomal Rearrangements in Mental Retardation and Autism (ASD)" are to know: i)
the percentage of CCRs among MR and ASD samples; ii) the influence of "chromosomal
phenotype" in their ascertainment. Patients with mental retardation were divided in two
groups, made up of 50 patients each, one (group 1) with a "chromosomal phenotype" and
the other (group 2) without dysmorphic features, all affected by MR, diagnosed according
to the DSM-IV-TR criteria.
The patients were included in the appropriate group according to the score reached
following the administration of the clinical checklist published by De Vries, in 2001. Each
subject reached a score between 0 and 10, depending on the presence or absence of some
clinical features such as MR in family history, small birth weight, abnormal postnatal
growth, facial dysmorphisms and congenital abnormalities.
We established a total score of 3 as cut-off, separating group 1 (scoring 3 or above)
from group 2 (scoring 2 or less).
Until now, we analyzed a total of 79 subjects (39 males and 40 females), 49 from group
1and 30 from group 2. A de novo CNVs, validated by MLPA, has been diagnosed in 20 (13
from group 1 and 7 from group 2) out of 79 MR patients.
The preliminary resulting percentages are: a de novo pathogenic CNVs is present in
25.3% (20/79) of MR patients, while in 26.5% (13/49) of group 1, and in 23.3% (7/30)
of group 2.
These preliminary results confirm that CCRs have an overall prevalence of 25.3% in
MR. Incidence of pathogenic CNVs actually was major in patients with a "chromosomal
phenotype". However, it should be noted that the sampling in the first group is almost
116
complete, while further 20 subjects should be tested in the second group, and this could
modify the results. Among 100 enrolled patients with Autism 30 subjects have been
analyzed having also MR and a "chromosomal phenotype". Three of them (10%) showed a
16p11.2 CNV (two deletions and one duplication).
117
INVESTIGATION OF GENETIC AND EPIGENETIC
MECHANISMS UNDERLYING BECKWITH-WIEDEMANN
SYNDROME (BWS) ON A LARGE COHORT
OF ITALIAN PATIENTS
Silvia Russo (a), Flavia Cerrato (b), Serena Ferraiuolo (a), Angela Sparago (b), Maria
Francesca Bedeschi (c), Faustina Lalatta (c), Donatella Milani (d), Angelo Selicorni (d), L.
Fedele (c), Andrea Riccio (b), Lidia Larizza (a)
(a) Laboratorio di Citogenetica e Genetica Molecolare Umana, IRCCS Istituto Auxologico
Italiano, Milano
(b) Dipartimento di Scienze Ambientali, Seconda Università degli Studi, Napoli
(c) Clinica Ostetrico-Ginecologica Università e Fondazione IRCCS, Ospedale Maggiore
Policlinico Mangiagalli e Regina Elena, Milano
(d) Clinica Pediatrica De Marchi, Università e Fondazione IRCCS, Ospedale Maggiore
Policlinico Mangiagalli e Regina Elena, Milano
118
iii) methylation analysis of 11 ICRs within a cohort of 149BWS patients, including 81
with maternal hypomethylation of BWS Imprinting Centre 2. Both partial and complete
hypomethylation has been demonstrated in these cases, at PLAGL1 and GNAS/NESPAS
DMRs suggesting possible postzygotic origin of a mosaic imprinting error.
Lastly prenatal protocol has been approved by WP3, including the following steps: -
recruitment of cases referred by first level, ultrasound unit, foetal imaging, definition of
the complete foetal clinical picture, genetic counselling session, invasive procedures,
foetal karyotype at 400 band resolution, clinical genetics evaluation, clinical pathology
protocol, and follow-up after delivery or termination. Investigation of 10 foetuses with
evidence of omphalocele plus other anomalies in two.led to disclose the molecular
mechanism in three of them, with two showing hypomethylation of KvDMR1 and one
carrying a CDKN1C mutation.
119
P. TWO INTRAGENIC NIPBL DELETIONS
AND ONE CONTIGUOUS GENE SYNDROME
DETECTED BY MLPA IN CDLS PATIENTS
Silvia Russo (a), Cristina Gervasini (b), Maura Masciadri (a), Paola Castronovo (b),
Donatella Milani (c), Anna Cereda (c), Giuseppe Zampino (d), Angelo Selicorni (c), Lidia
Larizza (a,b)
(a) Laboratorio di Citogenetica e Genetica Molecolare Umana, IRCCS Istituto Auxologico
Italiano, Milano
(b) Università degli Studi, Milano
(c) Dipartimento di Pediatria, Fondazione IRCCS, Ospedale Maggiore Policlinico
Mangiagalli e Regina Elena, Milano
(d) Dipartimento di Pediatria, Università Cattolica del Sacro Cuore, Roma
120
INCREASED THROMBIN GENERATION IN SEVERE
HEMOPHILIACS WITH MILD CLINICAL PHENOTYPE
Elena Santagostino (a), Maria Elisa Mancuso (a), Armando Tripodi (a), Veena
Chantarangkul (a), Gianluigi Pasta (b), Simona Maria Siboni (a), Pier Mannuccio Mannucci (a)
(a) Centro Emofilia e Trombosi Angelo Bianchi Bonomi, Fondazione IRCCS, Ospedale
Maggiore Policlinico Mangiagalli e Regina Elena, Università degli Studi, Milano
(b) Dipartimento di Traumatologia, Fondazione IRCCS, Ospedale Maggiore Policlinico
Mangiagalli e Regina Elena, Università degli Studi, Milano
121
AUTOSOMAL RECESSIVE SPASTIC PARAPLEGIA
WITH THINNING OF CORPUS CALLOSUM
AND PERIVENTRICULAR WHITE MATTER
CHNAGES. CLINICAL, MOLECULAR,
AND NEUROIMAGING STUDIES
Filippo M. Santorelli (a), Paola Denora (a,b), Gabriella Silvestri (c), Federico Zara (d),
Francesco G. Garaci (e), Giovanni Stevanin (b)
(a) Medicina Molecolare e Neuroscienze, Ospedale Pediatrico Bambino Gesù, IRCCS,
Roma
(b) Institut National de la Santé et de la Recherche Médicale, INSERM, Paris, France
(c) Istituto di Neurologia, Università Cattolica del Sacro Cuore, Roma
(d) Malattie Neurogenetiche e Neurodegenerative, Istituto Giannina Gaslini, Ospedale
Pediatrico IRCCS, Genova
(e) Unità di Neuroimmagini, Università degli Studi Tor Vergata, Roma
122
TESTING IN VITRO AND IN VIVO TREATMENTS
FOR INCLUSION BODY MYOSITIS
Simona Saredi (a), Claudia Di Blasi (a), Pia Bernasconi (a), Lucia Morandi (a), Renato
Mantegazza (a), Marina Mora (a), Cristina Sancricca (b), Enzo Ricci (b), Pietro Attilio
Tonali (b), Massimiliano Mirabella (b)
(a) Unità Operativa Malattie Neuromuscolari e Neuroimmunologia, Fondazione IRCCS,
Istituto Neurologico Carlo Besta, Milano
(b) Dipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, Roma
Evaluation of Nitric Oxide (NO), using the Griess test, in muscle cell cultures obtained
from 9 sporadic Inclusion Body Myositis (sIBM) and 6 hereditary IBM (hIBM) GNE-
mutated patients, each compared to an age-matched control cell culture, showed that the
amount of NO produced by the sIBM myoblasts was always increased compared to the
control, but with marked individual variability (20%-80% increase relative to the control
cells). In muscle cells from 2 dermatomyositis and 3 polymyositis patients, values between
patient and control in a given test were always similar, while in hIBM myoblasts there was
a constant 20% increase in NO production. Evaluation of expression of HemeOxigenase-1
(HO-1), a ubiquitous enzyme involved in cell detoxification mechanisms and activated by
several factors including NO, showed increased numbers of sIBM cells strongly expressing
HO-1 by immunocytochemistry, and, by RT-PCR, increase in HO-1 mRNA levels in sIBM
but not in hIBM cells. From June 2006 we have enrolled 13 patients affected by sIBM for
simvastatin treatment, and 3 IBM patients are undergoing intravenous immunoglobulin
(IVIG 2g/Kg) treatment every two months. Eight patients have reached the daily dose of 40
mg simvastatin and 5 patients are still gradually increasing the dosage. According to the
protocol established by the International Myositis Outcome Assessment Collaborative
Study (IMACS), the patients are evaluated every two months by manual muscle testing,
self-report questionnaires and blood tests for CK, lipids, liver and renal functions. We are
also currently validating six core set measures (disease activity measures), developed by
IMACS, that capture disease activity and another IMACS core set of "disease damage
measures" for assessment of persistent changes in anatomy, physiology, pathology or
function. None of the patients have reported clinically significantly side effects during
simvastatin treatment. Only one patient has shown a significant CK increase. Three patients
have undergone 4 to 6 infusions of IVIG therapy with no relevant side effects, except for 1
patient who developed high blood pressure values during the treatment, controlled with
adequate therapy. Regarding clinical evolution, in none of the patients on simvastatin we have
observed so far a worsening of the clinical condition, in 3 patients we have observed a slight
improvement of muscular strength, while 2 patients refer a subjective improvement of general
conditions and in managing common daily activities. No significant clinical variations has
been observed in the other patients either on simvastatin or on IVIG every two-months.
123
IDENTIFICATION OF GENETIC FACTORS
RESPONSIBLE FOR RARE DISORDERS
WITH CONGENITAL HEART DEFECTS
Anna Sarkozy (a), Francesca Lepri (a,b), Alessandro De Luca (a), Maria Cristina Digilio (c),
Marco Tartaglia (d), Bruno Dallapiccola (a,b)
(a) Ospedale Casa Sollievo della Sofferenza, IRCCS, San Giovanni Rotondo, Foggia, e
Istituto Casa Sollievo della Sofferenza Mendel, Roma; Università degli Studi Sapienza,
Roma
(b) Dipartimento di Medicina Sperimentale e Patologia, Università degli Studi La
Sapienza, Roma
(c) Ospedale Pediatrico Bambino Gesù, IRCCS, Roma
(d) Dipartimento di Biologia Cellulare e Neuroscienze, Istituto Superiore di Sanità, Roma
124
patients, including a novel in-frame insertion in a four year old subject. According with
previous observations, CFC patients were found to be mutated in either BRAF, MEK1 or
MEK2 genes.
Preliminary genotype-phenotype correlation analyses indicate that MEK and BRAF gene
mutations are associated with overlapping clinical features.
125
IMPROVING DIAGOSTIC SKILLS FOR INHERITED
THROMBOCYTOPENIAS
Anna Savoia (a), Daniela De Rocco (a), Mariateresa Di Stazio (a), Federica Melazzini (b),
Alessandro Pecci (b), Patrizia Noris (b), Carlo L. Balduini (b)
(a) Dipartimento di Scienze Riproduttive e dello Sviluppo, Università degli Studi, Trieste
(b) Dipartimento di Medicina Clinica, Fondazione IRCCS, Policlinico San Matteo,
Università degli Studi, Pavia
The results obtained so far are described according to the specific aims of the project
as follows:
Identification and etiologic characterization of inherited thrombocytopenias not yet
described. Two new genes, each responsible for novel forms of autosomal dominant
thrombocytopenias, have been identified through linkage analysis and mutation screening of
the candidate regions (manuscripts in preparation).
Identification of genes responsible for inherited thrombocytopenias that have been
described previously but whose etiology is still unknown. We have identified a family
with a suspected diagnosis of "gray platelet syndrome". The clinical and morphological
platelet features were characterized. A positional cloning strategy is being carried out to
identify the gene.
Characterization of the mutations causing inherited thrombocytopenia in Italy. We
identified mutations of the c-MPL gene and clonal chromosomal anomalies in five families
with Congenital Amegakaryocytic Thrombocytopenia (CAMT). Moreover, we have extended
the database of Italian Registry of MYH9-Related Disease (MYH9RD) to 108 patients. In
order to validate the presence of MYH9 aggregates in neutrophils as a patognomonic feature
of the disease, we are also sequencing the entire MYH9 gene in 30 patients with the clinical
features of MYH9RD but with a normal distribution of the protein. We have also excluded
the presence of mutations of cytochrome C (CYCS) in 70 patients with features similar to
those observed in patients with a detective CYCS.
Identification of genotype/phenotype correlations in patients affected by diseases with
known etiology and wide phenotypic variability. In 108 MYH9RD patients we identified a
significant correlation between phenotype and genotype at least for the most four common
mutations affecting 70% of patients. Thus, the risk of developing kidney failure, cataracts,
deafness, and severe bleeding tendency may be predicted. Since some drugs modify the
clinical course of kidney damage, patients recognized at risk of renal failure could undergo
treatments to prevent or postpone the dysfunction. The genotype and phenotype correlation
was also performed in CAMT patients. In this study we did not confirm previous reports and
suggested that hematopoietic stem cell transplantation should not be postponed even in those
patients whose c-MPL mutations may predict residual activity of c-MPL.
126
CHARACTERIZATION OF PRELAMIN A FORMS
ACCUMULATED IN MANDIBULOACRAL DYSPLASIA
AND PROSPECTS FOR THERAPY
Elisa Schena (a), Vittoria Cenni (b), Marta Columbaro (b), Daria Camozzi (a), Cristina
Capanni (b), Stefano Squarzoni (b), Anne Vielle (c), Tiziana Greggi (c), M. Rosaria
D'Apice (d), Giuseppe Novelli (d), Nadir M. Maraldi (a,b), Giovanna Lattanzi (b)
(a) Laboratorio di Biologia Cellulare, Istituto Ortopedico Rizzoli, Bologna
(b) Istituto di Genetica Molecolare, IGM, Consiglio Nazionale delle Ricerche, Sezione di
Bologna c/o Istituti Ortopedici Rizzoli, Bologna
(c) Divisione di Chirurgia Ortopedico-Traumatologica Vertebrale, Istituto Ortopedico
Rizzoli, Bologna
(d) Dipartimento di Biopatologia e Diagnostica per Immagini, Università degli Studi Tor
Vergata, Roma
127
MOLECULAR CHARACTERIZATION OF A LARGE
COHORT OF CORNELIA DE LANGE SYNDROME
ITALIAN PATIENTS AND RELATED PHENOTYPES
Angelo Selicorni (a), Silvia Russo (b), Cristina Gervasini (c), Maura Masciadri (b), Paola
Castronovo (c), Anna Cereda (a), Alice Passarini (a), Donatella Milani (a), Lidia Larizza (b,c)
(a) I Clinica Pediatrica, Fondazione IRCCS, Ospedale Maggiore Policlinico Mangiagalli e
Regina Elena, Milano
(b) Laboratorio di Citogenetica e Genetica Molecolare Umana, IRCCS Istituto Auxologico
Italiano, Milano
(c) Genetica Medica, Azienda Ospedaliera San Paolo, Polo Universitario, Università degli
Studi, Milano
128
IMMUNOBIOLOGIC AND CLINICAL ACTIVITY
OF DNA HYPOMETHYLATING AGENTS
IN HUMAN SARCOMAS
Luca Sigalotti (a), Giulia Parisi (a), Francesca Colizzi (a), Elisabetta Fratta (a,b), Hugues
J.M. Nicolay (a,b), Alessia Covre (a,b), Sandra Coral (a), Vincenzo Canzonieri (c), Michele
Maio (a,b)
(a) Unità di Bioimmunoterapia del Tumore, Dipartimento di Oncologia Medica, Centro di
Riferimento Oncologico, IRCCS, Aviano, Pordenone
(b) Divisione Oncologia Medica e Immunoterapia, Dipartimento di Oncologia, Ospedale,
Istituto Toscano Tumori, Università degli Studi, Siena
(c) Divisione di Patologia, Centro di Riferimento Oncologico, IRCCS, Aviano, Pordenone
129
of HLA class I antigens and up-regulated/induced the expression of ICAM-1 in the panel of
sarcoma cell lines under investigation.
These data, though preliminary, strongly suggest that DHA may represent useful
therapeutic agents to comprehensively increase immunogenicity and immune recognition of
sarcoma cells, providing the rationale for their use in new combined chemo-
immunotherapeutic approaches in the sarcoma clinic.
130
GENETIC ANALYSIS OF ARRHYTHMOGENIC
INHERITED DISEASES
Elena Sommariva (a), Sara Benedetti (b), Francesco Sacco (a), Daniele Zeni (b), Chiara
Redaelli (b), Simone Sala (a), Maurizio Ferrari (b,c,d), Carlo Pappone (a)
(a) Unità di Aritmiologia, Dipartimento di Cardiologia, Fondazione San Raffaele del
Monte Tabor, IRCCS, Milano
(b) Laboratorio di Biologia Clinica e Molecolare, Diagnostica e Ricerca, Fondazione San
Raffaele del Monte Tabor, IRCCS, Milano
(c) Unità per la Diagnosi Genomica delle Malattie Umane, Fondazione San Raffaele del
Monte Tabor, IRCCS, Milano
(d) Università Vita-Salute San Raffaele, Fondazione San Raffaele del Monte Tabor, IRCCS,
Milano
131
EVALUATION AND REHABILITATION
OF SWALLOWING DYSFUNCTION IN PATIENTS
WITH RARE NEUROLOGICAL DISORDERS
AND MOVEMENT DISORDERS
In recent years there has been increasing awareness of the feeding difficulties
experienced by patients with neurological disorders children with neurodevelopmental
disability and adults with movement disorders.
The majority of the studies have been in children with cerebral palsy and in patients
with parkinsonism in particular Progressive Supranuclear Palsy (PSP). Many have been
found to have major problems with eating and swallowing.
Only a few studies have suggested that nutritional problems are also frequent in patients
with inherited neuromuscular disorders. Patients with Duchenne muscular dystrophies,
spinal muscular atrophy, congenital muscular dystrophies and other congenital myopathies
often have feeding difficulties, gastrointestinal dysfunction and excessive or reduced
weight gain but this has not been systematically explored.
Patients with PSP can develop a severe impairment of speech and swallowing. These
problems are linked to neuronal damage within the brainstem and their connection to higher
brain centres, especially the basal ganglia.
The work will be carried on into 2 workpackages, one focusing on the assessment and
rehabilitation of feeding difficulties in the different forms of neuromuscolar disease and the
other relating these aspects to patients with PSP and to the various phenotypes observed in
the different forms of neuromuscular diseases and top other aspects of clinical
management.
The aims of this study are:
– to conduct a survey using a questionnaire on feeding difficulties, gastrointestinal
involvement and weight gain in a large cohort of neuromuscular and PSP patients;
– to assess swallowing problems by use of clinical and instrumental tools;
– to correlate these findings with other variables such as age, level of motor
impairment, use of ventilatory support and other aspects of clinical management
such as scoliosis, heart involvement etc.;
– to evaluate quality of life (qol) and validate in Italian two English language specific
questionnaires (swall qol and swall-care questionnaire);
– to suggest therapeutic options and management guidelines according to the results of
the research.
Today 10 patients with PSP has been evaluated. Clinical evaluation has been done using
the "Progressive Supreanuclear Palsy Rating Scale and Staging System" (Range 0-100;
stage 1-5).
132
Moreover the following instrumentasl evaluations have been carried out: FEES
(Fiberoptic Endoscopic Evaluation of Swallowing), Dysphagie Limit, EMG
(Elettromiografia).
133
PCBS AS POSSIBLE EXOGENOUS RISK FACTORS
IN THE BLADDER EXTROPHY-EPISPADIAS
COMPLEX PATHOGENESIS: THE BLADE PROJECT
Sabrina Tait (a), Cinzia La Rocca (a), Vincenzo Lagatta (a), Michaela Luconi (b), Elaine
M. Faustman (c), Mario Maggi (b), Alberto Mantovani (a)
(a) Dipartimento di Sanità Pubblica Veterinaria e Sicurezza Alimentare, Istituto Superiore
di Sanità, Roma
(b) Dipartimento di Clinica Fisiopatologia, Università degli Studi, Firenze
(c) Institute for Risk Analysis and Risk Communication, Department of Environmental and
Occupational Health Sciences, University of Washington, Seattle, WA, USA
134
Western Blot assays are evaluating possible protein modulation of the Fgfs and
Bmps target proteins. Preliminary results will be presented.
The work is supported by the project The Bladder Extrophy-Epispadias Complex and Exogenous
Risk Factors (BLADE), within the framework of the ISS-NIH Collaborative Programme on Rare
diseases (2007-9).
135
TACKLING RARE DISEASES YET LACKING
DIAGNOSIS AND/OR PROGNOSIS:
A PILOT PROJECT INTEGRATING DATA
COLLECTION AND EXPERIMENTAL STUDIES
Domenica Taruscio (a), Antonio Antoccia (b), Gianluca Azzalin (c), Rita Devito (d),
Alessandra Di Masi (b), Stefano Lorenzetti (e), Giuseppe Macino (c), Armando Magrelli (a),
Alberto Mantovani (e), Francesca Maranghi (e), Gabriele Moracci (e), Sara Nicolai (b),
Caterina Tanzarella (b), Marco Salvatore (a), Roberta Tassinari (e), Fabrizio Tosto (a),
Mara Viganotti (a)
(a) Centro Nazionale Malattie Rare, Istituto Superiore di Sanità, Roma
(b) Università degli Studi Roma Tre, Roma
(c) Sezione di Genetica Molecolare, Dipartimento di Biotecnologie Cellulari ed
Ematologia, Policlinico Umberto I, Roma
(d) Ospedale Pediatrico Bambino Gesù, IRCCS, Roma
(e) Dipartimento di Sanità Pubblica Veterinaria e Sicurezza Alimentare, Istituto Superiore
di Sanità, Roma
Hepatoblastoma (HB) is the most common primary hepatic tumor in children, with most
cases occurring before 2 years of age. Most HB cases are sporadic even though association
with other rare diseases (BWS, FAP) have been studied. Subjects with sporadic HBs have a
high-frequency of mutations of β-catenin gene. Alteration of IGF2, a peptide hormone
crucial for normal development, including enhanced expression and altered promoter-
specific transcriptional patterns, have been found in HB as well as in other tumours.
Our integrated study aims: i) to elucidate signalling pathway(s) and molecular
mechanism(s) of HB induction and progression with special attention to the role of Wnt/β-
catenin and IGF pathways; ii) to characterize possible early markers for HB diagnosis
and/or prognosis; iii) to establish a chemically-induced mouse model of HB. Herewith we
present the preliminary findings of the project.
Analyses were performed on nine liver tissues samples, obtained from HB patients
(aged 8-39 mo) recruited at Bambino Gesù Hospital.
Mutations leading to constitutive activation of β-catenin occur with high frequency in
HB and are mainly characterized by point mutations and deletions on exon 3 and its
flanking regions. β-catenin gene was amplified and sequenced in all HB liver tissues and no
mutations on exon 3 have been detected in tumor tissue. IGF2 gene transcription, is
triggered by four distinct promoters in a tissue- and developmental-specific manner, and is
controlled by DNA methylation and altered promoter-specific transcriptional patterns
frequently occur in cancer. DNA was analysed with Methylation-Specific PCR (MSP)
assays and promoter-specific levels of IGF2 transcription has been evaluated by qPCR.
MicroRNAs are short noncoding RNAs that are believed to serve fundamental roles in
many biological processes through regulation of gene expression. In order to clarify their
role in HB we profiled by an high-throughput method microRNAs expression in HBs and
control tissues. We analysed differentially expressed microRNAs and their putative targets
136
in normal and tumor tissue. Some of these microRNAs, as well as some of their targets,
shows an alteration of their expression levels in the analysed samples. Preliminary data
show an active role of these microRnas in the Wnt/b-catenin and IGF signalling pathways.
An immunoprecipitation assay for β-catenin was carried out in the tumor tissues and in
the normal counterparts from three HB patients. A reduced amount of β-catenin was
detected in 2 out of 3 patients. A similar trend was found for c-Jun and Cyclin D1 proteins,
both trascriptionally regulated by β-catenin. Interestingly, an increased amount of the
growth factor receptor-2 protein (GRB-2), a mitogenic marker, was expressed in HB
tumors compared to the normal tissues. Plag-1 protein, whose overexpression may be
responsible for IGF-2 expression in HB, was down-regulated in the three HB. Finally, we
observed a significant reduction of PDCD4 protein, whose expression is controlled by
microRNA-21.
Finally, a chemically-induced mouse model of HB has been established in order to
investigate if the molecular events evidenced in the previous WPs in human HB liver
tissues, as previously mentioned, occurs also in an animal model exposed to di-2-ethyl-exyl
phthalate (DEHP), a plasticizer which, besides being a widespread pollutant, is contained in
medical devices used for parenteral nutrition of pre-term neonates: indeed, both pre-term
condition and exposure to DEHP have been recently suggested to be environmental risk
factors highly associated to HB. Our DEHP-based mouse model shows features to another
rodent model of intra-uterine growth retardation (IGF2 knockout in Sprague-Dawley rats),
including impaired β-catenin signalling pathways.
This work is performed within the frame of the project "Tackling rare diseases yet lacking
diagnosis and/or prognosis: a pilot project integrating data collection and experimental studies"
supported by a NIH-ISS 2007-2009 grant.
137
P. THE ITALIAN NATIONAL REGISTRY
OF AMYOTROPHIC LATERAL SCLEROSIS
138
THERAPY-ORIENTED LARGE SCALE GENOMIC
AND GENE EXPRESSION ANALYSIS IN THYMOMAS,
MESOTHELIOMAS AND LUNG CARCINOIDS
Francesca Toffalorio (a,b), Elena Belloni (a), Caterina Fumagalli (c), Soheil Javan (a),
Carla Micucci (a), Simone Paolo Minardi (a), Myriam Alcalay (a), Giuliana Pelicci (a),
Giuseppe Pelosi (c), Lorenzo Spaggiari (d), Filippo de Braud (b), Tommaso De Pas (b)
(a) Dipartimento di Medicina Molecolare, Campus IFOM-IEO, Istituto Europeo di
Oncologia, Milano
(b) Dipartimento di Medicina Oncologica, Campus IFOM-IEO, Istituto Europeo di
Oncologia, Milano
(c) Dipartimento di Patofisiologia, Campus IFOM-IEO, Istituto Europeo di Oncologia,
Milano
(d) Dipartimento di Chirurgia Toracica, Campus IFOM-IEO, Istituto Europeo di
Oncologia, Milano
Thymomas, mesotheliomas and lung carcinoids are rare tumors and surgical resection is
to date the only curative option for their treatment. When surgery is not feasible, common
strategies for their cure are missing, since chemotherapy efficacy is often not satisfactory.
Due to the low incidence and prevalence of these tumors, drug efficacy and treatment
strategy cannot be demonstrated by large scale clinical trials, as suggested by the criteria of
"evidence based" medicine.
We proposed a genetic approach in order to identify genes that may play a role in
tumorigenesis and, more importantly, that can become effective "drugable" targets, in these
different tumor types.
In this context, we performed gene expression microarray analysis in order to identify,
within the different tumor types, new categories with specific gene signatures, which are
expected to greatly improve the knowledge of the tumors, mainly in terms of disease
development and progression (aggressiveness). We started our analysis exploring gene
expression profiling among lung carcinoids, since we already had a good collection of
samples.
Using a 54,000 probe set (Affymetrix Human GeneChip U133 2.0), we have analyzed a
first group of lung carcinoids, constituted of:
– 4 typical carcinoids;
– 4 atypical carcinoids;
– 8 corresponding normal counterparts.
Our preliminary results show that:
– typical carcinoids are relative homogenous according to the detected gene
expression profile. On the contrary, atypical carcinoids resulted different from one
to another;
– the expression profile of normal lung tissue is homogenous and different from both
typical and atypical carcinoids.
139
These preliminary results are intriguing, so they prompted us to test a higher number of
samples. in any case, based on these initial data, we expect to identify a typical-carcinoids-
specific signature, evidencing the role of particular pathways that could become new
therapeutic targets. atypical carcinoids appear to be a complete different disease and our
aim is that to, by enlarging the samples size, identify sub-groups with common features. the
experiments are ongoing.
140
PHENOTYPE CORRECTION OF ADAMTS13
DEFICIENCY AND PROTECTION
FROM THE DEVELOPMENT OF THROMBOTIC
THROMBOCYTOPENIC PURPURA
THROUGH INTRAVASCULAR AND SKELETAL
MUSCLE ADAMTS13 GENE DELIVERY IN MICE
Piera Trionfini (a), Susanna Tomasoni (a), Miriam Galbusera (a), Roberta Donadelli (a),
Daniela Corna (a), Lorena Zentilin (b), David Motto (c), Mauro Giacca (b), Giuseppe
Remuzzi (a), Ariela Benigni (a)
(a) Istituto di Ricerche Farmacologiche Mario Negri, Bergamo
(b) Laboratorio di Medicina Molecolare, International Centre for Genetic Engineering and
Biotechnology, ICGEB, Trieste
(c) Department of Internal Medicine, University of Iowa Carver College of Medicine, Iowa
City, IA, USA
141
the ADAMTS13 ability to cleave VWF. The lack of detectable levels of the recombinant
protein could be due to a low infectivity of the AAV vector.
Indeed, one main limitation of rAAV2 is represented by its native packaging capacity
restricted to 4.7 kB, the same size of ADAMTS13 cDNA and this could interfere with the
vector infectivity. A recent report described the possibility to obtain more effective vectors
using different serotype such as rAAV2/5.
This hypothesis will be tested. We are now going to test the efficacy of adenoviral
vectors in producing active ADAMTS13 protein in knockout mice.
142
P. AMYOTROPHIC LATERAL SCLEROSIS
IN ITALY: PREVALENCE AND INCIDENCE BASED
ON ADMINISTRATIVE DATA SOURCES
Monica Vichi (a), Nicola Vanacore (a), Susanna Conti (a), Luisa Frova (b), Lucia Lispi (c),
Paolo Salerno (d), Domenica Taruscio (d), Maria Masocco (a)
(a) Centro Nazionale di Epidemiologia, Sorveglianza e Promozione della Salute, Istituto
Superiore di Sanità, Roma
(b) Direzione Centrale per le Statistiche e le Indagini sulle Istituzioni Sociali, Istituto
Nazionale di Statistica, ISTAT, Roma
(c) Direzione Generale della Programmazione Sanitaria, dei Livelli di Assistenza e dei
Principi Etici di Sistema, Ministero del Lavoro, Salute e Politiche Sociali, Roma
(d) Centro Nazionale Malattie Rare, Istituto Superiore di Sanità, Roma
We combined information from Italian Hospital Discharge Records (HDR) and Death
Certificates in order to estimate motor neuron disease occurrence.
32066 HDR with ICD9-CM 335.2_ code were extrapolated from about 60 million in the
period 2001-2005. The "hospitalisation paths" of the patients (all the diagnosis and
procedures from the first to the last hospitalization) were analysed and a record linkage
with Death Certificates was performed in order to exclude unreliable diagnosis and ALS-
mimic syndromes. After selection, 9274 patients were considered in analysis.
Incidence was estimated as a mean of new hospitalized cases in 2003-2004 (that is a
proxy of incidence in 2002-2003, hypothesizing a 12-months delay from onset to first
hospitalization), while prevalence at 01/01/2003 was estimated by summing patients
hospitalized for the first time during 2003 (incident cases in 2002) and patients hospitalized
before 2003 that were found alive after 31/12/2002 (for a second hospitalization or
undetectable among linked Death Certificates).
For Amyotrophic Lateral Sclerosis we found about 1,360 cases hospitalized for the first
time during 2003 and 1,390 hospitalized for the first time during 2004, corresponding to a
mean incidence rate of 2.4 per 100,000 inhabitants. About 4,000 ALS patients were found
alive at 1/1/2003 corresponding to a prevalence rate of 7.0 per 100,000 inhabitants.
Our findings are consistent with those deriving from ALS-Registries.
143
COMBINED TREATMENT WITH STATINS
AND AMINOBISPHOSPHONATES
IN MANDIBULOACRAL DYSPLASIA FIBROBLASTS
Anne Vielle-Canonge (a), Francesca Gullotta (a), Silvia Salvatori (b), Paolo Molinaro (b),
Francesca Lombardi (a), Silvia Ciacci (b), Anna Maria Nardone (b), Monica D'Adamo (c),
Paolo Sbraccia (c), Maria Rosaria D'Apice (b), Giovanna Lattanzi (d), Nadir M. Maraldi (d),
Giuseppe Novelli (a,b,e)
(a) Dipartimento di Biopatologia e Diagnostica per Immagini, Università degli Studi Tor
Vergata, Roma
(b) Dipartimento di Genetica Medica, Azienda Ospedaliera Universitaria, Policlinico Tor
Vergata, Roma
(c) Dipartimento di Medicina Interna, Università degli Studi Tor Vergata, Roma
(d) Istituto di Genetica Molecolare, IGM, Consiglio Nazionale delle Ricerche, Sezione di
Bologna c/o Istituti Ortopedici Rizzoli, Bologna
(e) University of Arkansas for Medical Sciences, Little Rock, AR, USA
144
THERAPEUTIC POTENTIAL OF STEM CELL FACTOR
IN THE HUMAN BETA-THALASSEMIA TREATMENT:
IN VITRO AND IN VIVO STUDIES
Ann Zeuner (a), Monica Bartucci (a), Ornella Morsilli (a), Nadia Maria Sposi (a), Marta
Baiocchi (a), Paolo Cianciulli (b), Ruggero De Maria Marchiano (a), Marco Gabbianelli (a)
(a) Dipartimento di Ematologia, Oncologia e Medicina Molecolare, Istituto Superiore di
Sanità, Roma
(b) Unità sulla Talassemia, Ospedale Sant'Eugenio, Roma
In the first part of this project we demonstrated that Stem Cell Factor (SCF) markedly
stimulates cell proliferation reactivating fetal hemoglobin (HbF) synthesis in human
thalassemic erythroid precursors; pharmacological doses of Dexamethasone (Dex)
potentiate these stimulatory effects, thus paving the way for a future clinical application of
SCF in beta-thalassemia treatment.
Hence, in order to design a protocol for pre-clinical studies in thalassemic mice, we
have performed in vivo experiments by evaluating the effects of SCF in C57/BL6 mice
treated with high doses of cisplatin, which induces a state of myelosuppression and
consequent anemia. This represents an optimal model for evaluating SCF ability to increase
haematological parameters such as Red Blood Cell (RBC) number and total hemoglobin
content. We observed that, by administering subcutaneous SCF doses of 50 μg/kg 4h before
and after cisplatin injection and every 8h for one week, RBCs increased from 7 to 10
x106/μl and Hb increased from 11 to 14 g/dl in SCF-treated mice, thus reaching normal
values. Moreover, preliminary results obtained by HPLC on normal mice treated with
SCF±Dex showed that this treatment induces a considerable reactivation of the beta-minor
globin chain synthesis. These results will be confirmed on thalassemic mice in the
following part of the project.
In parallel, we performed in vitro studies in which we analyzed the molecular
modifications induced by SCF in normal and thalassemic erythroid precursors grown in
unilineage culture of CD34+ hematopoietic progenitors. Our results obtained by RT-PCR
showed that in normal erythroid precursors SCF activates a set of genes including Notch2,
HES-1, IMPDH2, S100A and HMG (High Mobility Group) family members (HMGI-Y)
that play an essential role in the regulation of cell survival and proliferation.
Preliminary investigations performed on erythroblasts derived from two beta-major
thalassemic patients showed a stronger SCF mediated induction of Notch 2 as compared
with normal control.
The progressive iron overload is the most important complication in beta-thalassemic
patients but the relationship among ineffective erythropoiesis and iron-regulatory genes is
still unknown. In preliminary experiments we have investigated by Western Blot analysis
the protein levels of genes involved in iron metabolism and we found an increase of
Transferrin Receptor-1 (TFR-1) and ferroportin levels in SCF-treated cultures of erythroid
thalassemic progenitors.
145
These studies will be further developed in order to clarify the specific role of SCF-
induced genes in influencing cell survival, proliferation, HbF reactivation and iron
metabolism in beta-thalassemic patients.
146
AUTHORS' INDEX
147
Cammarota, R.; 3 Chiavetta, V.; 116
Camozzi, D.; 127 Chichierchia, G.; 91
Candi, E.; 23 Chiò, A.; 99
Canese, R.; 45 Chiodini, I.; 37
Canzonieri, V.; 129 Ciacci, S.; 144
Capanni, C.; 127 Ciana, G.; 14
Capasso, M.; 99 Cianchini, G.; 53
Capocaccia, R.; 67 Cianciulli, P.; 145
Capogrossi, M.C.; 68 Ciccolallo, L.; 67
Cappariello, A.; 24 Ciccone, R.; 116
Caprini, A.; 79 Cilli, M.; 43
Caprini, E.; 25 Cima, V.; 99
Caprioli, J.; 98 Cioni, A.; 75
Carbonari, M.; 25 Cipollone, R.; 23
Carbone, P.; 72 Cipriani, P.; 65
Cardone, F.; 27 Clerici, M.; 78
Carelli, S.; 70 Codispoti, A.; 23
Carlini, S.; 91 Colizzi, F.; 129
Carlo-Stella, N.; 13 Colombi, M.; 31
Carnemolla, B.; 102 Colombo, A.; 40
Carozzo, R.; 81 Colombo, M.P.; 19
Carta, C.; 29 Colucci, A.; 84
Casali, P.; 67 Columbaro, M.; 127
Casartelli, G.; 63 Comi, G.; 40
Casetta, I.; 99 Comi, G.P.; 21
Cassini, P.; 74 Conca, B.; 35
Castagnoli, L.; 29 Concardi, M.; 74
Castelletti, F.; 98 Confalonieri, M.; 14
Castiglia, D.; 31 Conte, R.; 102
Castiglia, L.; 116 Conti, S.; 91; 143
Castori, M.; 31 Coral, S.; 129
Castronovo, P.; 8; 57; 120; 128 Corbetta, S.; 37
Cattaneo, C.; 84 Cordeddu, V.; 29
Cattaruzza, S.; 104 Corna, D.; 141
Ceccarini, M.; 108 Corsolini, F.; 76
Cenni, V.; 127 Cortis, E.; 111
Censi, F.; 54; 58 Cosentino, F.I.I.; 114
Cereda, A.; 8; 120; 128 Costa, A.; 14
Ceribelli, A.; 91 Cotichini, R.; 99
Cerone, R.; 33 Covaciu, C.; 31
Cerrato, F.; 118 Coviello, S.; 40
Cerri, F.; 40 Covre, A.; 129
Cerutti, M.; 8; 10 Crippa, E.; 42
Chantarangkul, V.; 121 Crippa, M.P.; 56
Chessa, L.; 47 Croce, C.M.; 42
Chiarle, R.; 91 Crugnola, V.; 21
148
Cuomo, D.; 113 Di Rocco, G.; 68
Cutrona, G.; 43 Di Silvestre, M.; 75
D’Adamo, M.; 144 Di Stazio, M.; 126
D’Alessio, M.; 31 Di Virgilio, A.; 87
D’Ambrosio, A.; 87 Di Zenzo, G.; 53
D’Apice, M.R.; 127; 144 Didona, B.; 53
D’Arcangelo, G.; 61 Diegoli, M.; 74
D’Ascenzo, S.; 65 Digilio, M.C.; 29; 124
D’Errico, M.; 63 Disabella, E.; 74
Daga, A.; 43 Dogliotti, E.; 63
Dallapiccola, B.; 16; 29; 124 Dolo, V.; 65
Damonte, G.; 43 Donadei, S.; 96
Danesino, C.; 14 Donadelli, R.; 141
Dardis, A.; 14 Donzelli, O.; 71
de Braud, F.; 139 El-Hachem, M.; 31
De Caro, R.; 93 Eller-Vainicher, C.; 37
De Cecco, L.; 42 Eusepi, A.; 87
De Chiara, G.; 61 Evoli, A.; 91
De Felice, M.; 33 Facciolo, F.; 91
De Filippis, B.; 80 Fadda, P.; 25
De Luca, A.; 124 Failla, P.; 116
De Maria Marchiano, R.; 145 Fais, S.; 45
De Medici, D.; 55 Falbo, V.; 54; 58
De Mei, B.; 84 Fassina, G.; 3
De Milito, A.; 45 Faustman, E.M.; 134
De Pas, T.; 139 Favia, G.; 93
De Rocco, D.; 126 Fazio, R.; 40
De Sanctis, M.; 65 Fedele, L.; 118
De Vecchi, G.; 106 Fedeli, F.; 43
Degan, P.; 63 Feliciani, C.; 103
Dei Tos, P.A.; 67 Fenicia, L.; 55
Dejana, E.; 79 Ferini Strambi, L.; 114
Del Fattore, A.; 24 Fermo, E.; 6
Del Principe, D.; 111 Ferraccioli, G.; 65
Delia, D.; 47 Ferrai, C.; 56
Delibato, E.; 55 Ferraiuolo, S.; 57; 118
Denora, P.; 122 Ferrari, M.; 40; 131
Deraco, M.; 49 Ferrarini, M.; 43
DeVescovi, V.; 71 Ferretti, S.; 67
Devito, R.; 87; 136 Ferri, R.; 114
Di Benedetto, D.; 116 Ferrini, S.; 19
Di Blasi, C.; 123 Fichera, M.; 116
Di Giorgio, B.; 74 Filocamo, M.; 76
Di Giulio, A.M.; 70 Finocchiaro, G.; 17
Di Lauro, R.; 33 Fiorilli, M.; 25
Di Masi, A.; 51; 87; 136 Fiumara, A.; 14
149
Flex, E.; 29 Giorda, R.; 89
Floridia, G.; 54; 58 Giordani, L.; 111
Fodale, V.; 29 Giorgetti, S.; 96
Fogh, I.; 59 Giunti, A.; 71
Foresta, M.; 63 Giusti, I.; 65
Fortuna, A.; 81 Gorio, A.; 70
Fortunato, F.; 21 Govoni, V.; 99
Fortuzzi, S.; 106 Granchi, D.; 71
Foschini, M.P.; 58 Grandolfo, M; 72
Franceschini, C.; 114 Granone, P.; 91
Franchini, S.; 65 Grasso, M.; 74
Franchitto, A.; 47 Grasso, R.; 89
François, M.; 79 Greco, D.; 116
Frank, C.; 61 Greggi, T.; 75; 127
Fraticelli, P.; 65 Grossi, D.; 61
Fratta, E.; 129 Grossi, S.; 76
Frontani, M.; 25 Guarnieri, V.; 37
Frosina, G.; 63 Guerini, F.R.; 78
Frova, L.; 143 Guerrini, R.; 95
Frustaci, A.; 103 Guidoboni, M.; 104
Fumagalli, C.; 139 Guiducci, S.; 65
Gabbianelli, M.; 145 Gullotta, F.; 144
Gabrielli, A.; 65 Guzzetti, S.; 17
Galbusera, M.; 141 Hosking, B.; 79
Galesi, O.; 116 Iacobone, M.; 93
Gallo, E.; 91 Iacono, D.; 84
Gallo, P.; 84 Inghilleri, M.; 99
Gambardella, L.; 111 Iorio, A.; 110
Gambarin, F.; 74 Italian Patient's Associations
Gambaro, C.; 13 for Rare Diseases; 84
Gana, S.; 95 Javan, S.; 139
Garaci, F.G.; 122 Jocollé, G.; 49
Gariboldi, M.; 42 Kilstrup-Nielsen, C.; 35
Gatta, G.; 67 Koopman, P.; 79
Gatto, I.; 68 Kusamura, S.; 49
Gelb, B.D.; 29 La Bella, V.; 99
Gellera, C.; 59 La Rocca, C.; 134
Generini, S.; 65 Lacrima, K.; 104
Gentile, A.; 68 Lagalla, G.; 99
Gervasini, C.; 8; 57; 120; 128 Lagatta, V.; 87; 134
Gherzi, R.; 69 Lalatta, F.; 10; 118
Giacca, M.; 141 Lalle, M.; 91
Giacomelli, E.; 99 Landsberger, N.; 35
Giacomelli, R.; 65 Lanni, S.; 58
Giacomini, S.; 75 Lanzavecchia, A.; 53
Giammarioli, A.M.; 65 Lari, S.; 75
150
Larizza, L.; 8; 57; 118; 120; 128 Mantovani, A.; 51; 72; 86; 87; 134; 136
Lattanzi, G.; 127; 144 Manzini, C.; 102
Lattanzio, R.; 91 Maraldi, N.M.; 127; 144
Lauriola, L.; 91 Maranghi, F.; 51; 87; 136
Lavatelli, F.; 96 Marasini, B.; 13
Laviola, G.; 80 Marcoccia, D.; 87
Lemma, T.; 63 Marelli, S.; 89; 114
Leonardi, E.; 71 Mariani, M.R.; 43
Leone, M.; 99 Marini, C.; 95
Lepri, F.; 29; 124 Marino, M.; 45; 91
Lesma, E.; 70 Marra, M.; 54; 58
Liakouli, V.; 65 Marrelli, A.; 65
Licitra, L.; 67 Martella, G.; 113
Lispi, L.; 143 Martelli, M.; 91
Locatelli, C.; 55 Martikos, K.; 75
Logroscino, G.; 99 Martinelli, S.; 29
Loizzo, A.; 81; 82 Martucci, R.; 91
Loizzo, S.; 81; 82 Marziliano, N.; 74
Lombardi, F.; 144 Masciadri, M.; 57; 120; 128
Lombardo, G.A.; 25 Maselli, A.; 65
Lonati, D.; 55 Masi, G.; 93
Lorenzetti, S.; 51; 87; 136 Masocco, M.; 82; 143
Lozupone, F.; 45 Matis, S.; 43
Lucchini, V.; 21 Matucci-Cerinic, M.; 65
Luchetti, M.; 65 Mazzini, L.; 99
Luconi, M.; 134 Medda, E.; 33
Lusa, L.; 42 Mei, D.; 95
Luzi, A.M.; 84 Melazzini, F.; 126
Macchi, V.; 93 Melino, G.; 23
Macino, G.; 51; 87; 136 Menegatti, M.; 110
Macioce, P.; 108 Menni, F.; 10
Maggi, M.; 134 Mercuri, E.; 132
Magnani, M.; 71 Merlini, G.; 96
Magrelli, A.; 51; 87; 136 Merlo, D.; 61
Maio, M.; 104; 129 Merola, G.; 91
Maitz, S.; 10 Metere, A.; 111
Malesci, A.; 13 Miano, M.G.; 80
Malorni, W.; 65; 111 Micucci, C.; 139
Manca, S.; 78 Milani, D.; 10; 57; 118; 120; 128
Mancuso, M.E.; 121 Millimaggi, D.; 65
Mandrioli, J.; 99 Millo, E.; 43
Manfredi, A.A.; 65 Millul, A.; 12; 99
Mangione, P.; 96 Minardi, S.P.; 139
Mannucci, P.M.; 110; 121 Minetti, M.; 111
Manoukian, S.; 42; 106 Mingari, M.C.; 102
Mantegazza, R.; 123 Minisola, S.; 37
151
Mirabella, M.; 123 Palmieri, G.; 91
Moggio, M.; 21 Palù, G.; 93
Moglia, A.; 14 Pantaleoni, F.; 29
Molinaro, P.; 144 Pappone, C.; 131
Monaco, S.; 27 Parchi, P.; 27
Monsurrò, M.R.; 99 Parini, R.; 14
Mora, M.; 123 Parisi, G.; 129
Moracci, G.; 87; 136 Parisini, P.; 75
Morandi, L.; 123 Parrini, E.; 95
Moretti, F.; 35 Pasotti, M.; 74
Moroncini, G.; 65 Passarini, A.; 8; 128
Moroni, M.; 43 Pasta, G.; 121
Morsilli, O.; 145 Pazzaglia, C.; 103
Mosci, C.; 19 Pazzaglia, L.; 104
Mossali, C.; 98 Pecci, A.; 126
Motto, D.; 141 Pelicci, G.; 139
Mottolese, M.; 91 Pelosi, G.; 139
Mucignat, M.T.; 104 Perris, R.; 104
Narciso, L.; 63 Perrone Donnorso, R.; 91
Nardo, T.; 63 Perrone, F.; 49
Nardone, A.M.; 144 Perrone-Capano, C.; 80
Nasuelli, N.; 99 Persani, L.; 33
Natacci, F.; 17 Peruzzi, B.; 24
Nicolai, S.; 51; 87; 136 Peterlongo, P.; 106
Nicolay, H.J.M.; 129 Petrangeli, V.; 29
Nicolò, M.; 3 Petrigliano, R.; 84
Nicolosi, P.A.; 104 Petrucci, T.C.; 29; 108
Nisticò, L.; 82; 99 Pettinati, I.; 63
Noonan, D.M.; 3 Peviani, M.; 15
Noris, M.; 98 Peyvandi, F.; 110
Noris, P.; 126 Pfeffer, U.; 102
Notarangelo, L.; 101 Pianetti, G.; 98
Novelli, A.; 16 Piantelli, M.; 91
Novelli, G.; 127; 144 Piazza, T.; 19
Nuvolone, M.; 96 Piccardi, F.; 43
Obici, L.; 96 Picci, P.; 104
Olivieri, A.; 33 Pichierri, P.; 47
Oneda, R.; 63 Pierannunzio, D.; 138
Orecchia, P.; 102 Pierdominici, M.; 65
Orioli, D.; 63 Pierotti, M.A.; 42; 106
Orsenigo, F.; 79 Pietra, G.; 102
Orzan, F.; 17 Pietraforte, D.; 111
Padua, L.; 103 Pilotti, S.; 49
Palestro, G.; 91 Pilotto, A.; 74
Palla, R.; 110 Pingiotti, E.; 65
Palladini, G.; 96 Pipitone, E.; 75
152
Pisa, F.E.; 14 Romano, C.; 116
Pisa, R.; 91 Romeo, A.; 87
Pisani, A.; 113 Roncella, S.; 43
Piva, R.; 15 Ropolo, M.; 63
Pizzamiglio, S.; 106 Rosano, C.; 76
Platania, P.; 113 Rossi, B.; 99
Plazzi, G.; 114 Rovere-Querini, P.; 65
Pocchiari, M.; 27 Rubartelli, A.; 19
Podo, F.; 45 Ruco, L.; 91
Pomponio, G.; 65 Rufini, S.; 61
Pontieri, F.; 99 Rusciano, D.; 19
Popoli, P.; 113 Russo, G.; 25
Porcu, E.; 74 Russo, M.; 103
Porzionato, A.; 93 Russo, S.; 8; 57; 118; 120; 128
Powell, J.; 59 Sabbadini, M.G.; 65
Prata, C.; 81 Sacco, F.; 131
Previtali, S.; 40 Sala, S.; 131
Principe, S.; 27 Salerno, P.; 31; 82; 138; 143
Provinciali, L.; 99 Saletti, V.; 17
Puma, F.; 91 Salsano, E.; 17
Pupillo, E.; 12 Salvatore, M.; 51; 54; 72; 87; 136
Quattrini, A.; 40 Salvatori, S.; 144
Queirolo, P.; 19 Sampogna, F.; 25
Quinti, I.; 25 Sancricca, C.; 123
Racaniello, M.; 61 Sangiorgi, L.; 75
Radice, P.; 42; 106 Sanseverino, A.; 84
Raimondi, S.; 96 Santagostino, E.; 121
Rando, G.; 13 Santoni, A.; 101
Ratti, A.; 59 Santorelli, F.M.; 122
Ravaglia, S.; 14 Saredi, S.; 123
Ravagnani, F.; 106 Sarkozy, A.; 29; 124
Rea, V.; 102 Savoia, A.; 126
Redaelli, C.; 131 Sbraccia, P.; 144
Regis, S.; 76 Scarlato, M:; 40
Reid, J.F.; 42 Schena, E.; 127
Reitano, S.; 116 Schinocca, P.; 116
Remotti, D.; 91 Sciamanna, G.; 113
Remuzzi, G.; 98; 141 Scillitani, A.; 37
Rendina, E.; 91 Selicorni, A.; 8; 10; 57; 118; 120; 128
Ricceri, L.; 80 Serafini, E.; 74
Ricci, E.; 108; 123 Serio, A.; 74
Riccio, A.; 118 Sessa, M.; 76
Rigoldi, M.; 14 Siboni, S.M.; 121
Rinaldi, M.; 91 Sica, A.; 101
Riva, D.; 17 Sigalotti, Luca; 129
Rocino, A.; 110 Sigalotti, Lucia; 104
153
Silani, V.; 59 Tomasoni, S.; 141
Silvestri, G.; 122 Tonacchera, M.; 33
Sioletic, S.; 91 Tonali, P.A.; 123
Soddu, S.; 35 Torreri, P.; 29
Sola, P.; 99 Tosetti, F.; 3
Somma, L.; 65 Tosto, F.; 51; 54; 87; 136
Sommariva, E.; 131 Trionfini, P.; 141
Soncini, D.; 5 Tripodi, A.; 121
Sorarù, G.; 99 Trojsi, F.; 99
Sozzani, S.; 101 Truini, T.; 91
Spada, A.; 37 Tufarelli, D.; 132
Spaggiari, L.; 139 Tunesi, G.; 91
Sparago, A.; 118 Ugazio, A.; 24
Spataro, R.; 99 Uncini, A.; 99
Spiga, I.; 40 Uras, C.; 31
Sposi, N.M.; 145 Usai, S.; 78
Spreafico, M.; 110 Vaira, V.; 37
Squarzoni, S.; 127 Valentini, G.; 6; 65
Squittieri, F.; 59 Vanacore, N.; 82; 99; 138; 143
Stallcup, W.B.; 104 Venè, R.; 3
Stefanini, M.; 63 Verderio, P.; 106
Stella, L.; 29 Vettori, S.; 65
Stevanin, G.; 122 Vicentini, M.; 25
Stocchi, F.; 132 Vichi, M.; 82; 143
Stoppini, M.; 96 Viel, G.; 93
Straface, E.; 65; 111 Vielle, A.; 127
Svegliati, S.; 65 Vielle-Canonge, A.; 144
Tabolli, S.; 31; 53 Viganotti, M.; 51; 87; 136
Tagliani, M.; 74 Villa, L.; 8
Tagliavini, F.; 27 Villa, R.; 49
Tait, S.; 134 Villani, A.; 111
Tancredi, V.; 61 Viora, M.; 111
Tanzarella, C.; 51; 87; 136 Visentin, S.; 81
Tartaglia, M.; 29; 124 Vommaro, F.; 75
Taruscio, D.; 25; 31; 33; 51; 54; 58; 72; Zaffaroni, N.; 49
82; 84; 86; 87; 136; 138; 143 Zambruno, G.; 31; 53
Tassinari, R.; 51; 87; 136 Zampino, G.; 29; 120
Tassone, A.; 113 Zanella, A.; 6
Terrinoni, A.; 23 Zanusso, G.; 27
Teti, A.; 24 Zara, F.; 122
Toccaceli, V.; 99 Zeni, D.; 131
Tocco, V.; 25 Zentilin, L.; 141
Toffalorio, F.; 139 Zeuner, A.; 145
Toietta, G.; 68 Zoccolella, S.; 99
Tolusso, B.; 65 Zuffardi, O.; 116
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