En principe inoffensifs, certains bryozoaires, marins ou dulcicoles, peuvent néanmoins créer des nuisances, par exemple, en provoquant des allergies, en colonisant des coques de navires, en obstruant des conduites ou des prises d'eau ou... more
En principe inoffensifs, certains bryozoaires, marins ou dulcicoles, peuvent néanmoins
créer des nuisances, par exemple, en provoquant des allergies, en colonisant des coques de navires, en obstruant des conduites ou des prises d'eau ou en servant d'hôte intermédiaire à des parasites de poissons d'eau douce. D'autres, bien utiles, contiennent des substances aux potentialités thérapeutiques prometteuses.
The serine/threonine protein kinase C (PKC) family was first identified as intracellular receptor(s) for the tumor promoting agents phorbol esters. Thirty years after the discovery of PKC, the role of specific PKC isoforms has been... more
The serine/threonine protein kinase C (PKC) family was first identified as intracellular receptor(s) for the tumor promoting agents phorbol esters. Thirty years after the discovery of PKC, the role of specific PKC isoforms has been described in relationship with an altered pattern of expression in different types of cancer and a good number of small molecule inhibitors (inhibitory peptides, antisense oligonucleotides or natural compounds) targeting PKC are now available. Despite all these achievements and a huge amount of basic research studies on the biochemical regulation of PKC, there has been a delay in clinical trials with drugs targeting PKC function. This delay is easily explained taking into account the extreme biological complexity of the PKC family of isoforms and the incomplete understanding of the specific role of each PKC isozyme in different types of cancers. Some of the difficulties in developing pharmacological compounds selectively tuning the different PKCs have started to be overcome. In this review, the growing evidences of the role of the PKC isoforms α, βII, δ, , ζ and ι is in promoting or counteracting tumor progression will be discussed in relationship with promising therapeutic perspectives.