FOXP1 is an androgen-responsive transcription factor that negatively regulates androgen receptor signaling in prostate cancer cells (Q24315624)

negative regulation of androgen receptor signaling pathway

GOA release 2020-03-11

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GOA release 2020-03-11

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Yoshihide Hayashizaki

6

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author name string

Kenichi Takayama

1

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Kuniko Horie-Inoue

2

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Kazuhiro Ikeda

3

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Tomohiko Urano

4

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Kayoko Murakami

5

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Yasuyoshi Ouchi

7

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Satoshi Inoue

Biochemical and Biophysical Research Communications

8

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language of work or name

English

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publication date

19 September 2008

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published in

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volume

374

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issue

2

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page(s)

388-93

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cites work

Expression of the forkhead transcription factor FOXP1 is associated both with hypoxia inducible factors (HIFs) and the androgen receptor in prostate cancer but is not directly regulated by androgens or hypoxia

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Chromosome-wide mapping of estrogen receptor binding reveals long-range regulation requiring the forkhead protein FoxA1

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FoxA1 translates epigenetic signatures into enhancer-driven lineage-specific transcription

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Identification of region-specific transcription factor genes in the adult mouse brain by medium-scale real-time RT-PCR.

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Spatial and temporal recruitment of androgen receptor and its coactivators involves chromosomal looping and polymerase tracking

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Molecular determinants of resistance to antiandrogen therapy

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Identification of novel androgen response genes in prostate cancer cells by coupling chromatin immunoprecipitation and genomic microarray analysis

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Mechanisms of androgen-refractory prostate cancer

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Multiple Domains Define the Expression and Regulatory Properties of Foxp1 Forkhead Transcriptional Repressors

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Modulation of androgen receptor transactivation by FoxH1. A newly identified androgen receptor corepressor

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Androgen receptor signaling in androgen-refractory prostate cancer

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Transcriptional and DNA binding activity of the Foxp1/2/4 family is modulated by heterotypic and homotypic protein interactions

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Expression of the forkhead transcription factor FOXP1 is associated with estrogen receptor alpha and improved survival in primary human breast carcinomas

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Potentially oncogenic B-cell activation-induced smaller isoforms of FOXP1 are highly expressed in the activated B cell-like subtype of DLBCL.

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The Role of Hepatocyte Nuclear Factor-3α (Forkhead Box A1) and Androgen Receptor in Transcriptional Regulation of Prostatic Genes

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Coregulator recruitment and histone modifications in transcriptional regulation by the androgen receptor.

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Functional genomics identifies a mechanism for estrogen activation of the retinoic acid receptor alpha1 gene in breast cancer cells

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Identifiers

DOI

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Consolidated OpenCitations Corpus – April 2017

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Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

18640093

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Consolidated OpenCitations Corpus – April 2017