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Current perspectives on FOXA1 regulation of androgen receptor signaling and prostate cancer

FOXA1 (also known as hepatocyte nuclear factor 3α, or HNF-3α) is a protein of the FKHD family transcription factors. FOXA1 has been termed as a pioneer transcription factor due to its unique ability of chromatin remodeling in which the chromatin can be de-compacted to allow genomic access by nuclear...

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Detalles Bibliográficos
Autores principales: Yang, Yeqing Angela, Yu, Jindan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chongqing Medical University 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4477823/
https://www.ncbi.nlm.nih.gov/pubmed/26114156
http://dx.doi.org/10.1016/j.gendis.2015.01.003
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author Yang, Yeqing Angela
Yu, Jindan
author_facet Yang, Yeqing Angela
Yu, Jindan
author_sort Yang, Yeqing Angela
collection PubMed
description FOXA1 (also known as hepatocyte nuclear factor 3α, or HNF-3α) is a protein of the FKHD family transcription factors. FOXA1 has been termed as a pioneer transcription factor due to its unique ability of chromatin remodeling in which the chromatin can be de-compacted to allow genomic access by nuclear hormone receptors, including androgen receptor (AR) and estrogen receptor (ER). In this review, we discuss our current understanding of FOXA1 regulation of prostatic and non-prostatic AR-chromatin targeting. We present an updated model wherein FOXA1:AR equilibrium in the nuclei defines prostatic AR binding profile, which is perturbed in prostate cancer with FOXA1 and/or AR de-regulation. Finally, we discuss recent efforts in exploring new horizons of AR-independent functions of FOXA1 in prostate cancer and interesting directions to pursue in future studies.
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spelling pubmed-44778232015-06-23 Current perspectives on FOXA1 regulation of androgen receptor signaling and prostate cancer Yang, Yeqing Angela Yu, Jindan Genes Dis Article FOXA1 (also known as hepatocyte nuclear factor 3α, or HNF-3α) is a protein of the FKHD family transcription factors. FOXA1 has been termed as a pioneer transcription factor due to its unique ability of chromatin remodeling in which the chromatin can be de-compacted to allow genomic access by nuclear hormone receptors, including androgen receptor (AR) and estrogen receptor (ER). In this review, we discuss our current understanding of FOXA1 regulation of prostatic and non-prostatic AR-chromatin targeting. We present an updated model wherein FOXA1:AR equilibrium in the nuclei defines prostatic AR binding profile, which is perturbed in prostate cancer with FOXA1 and/or AR de-regulation. Finally, we discuss recent efforts in exploring new horizons of AR-independent functions of FOXA1 in prostate cancer and interesting directions to pursue in future studies. Chongqing Medical University 2015-02-04 /pmc/articles/PMC4477823/ /pubmed/26114156 http://dx.doi.org/10.1016/j.gendis.2015.01.003 Text en Copyright © 2015, Chongqing Medical University. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Yang, Yeqing Angela
Yu, Jindan
Current perspectives on FOXA1 regulation of androgen receptor signaling and prostate cancer
title Current perspectives on FOXA1 regulation of androgen receptor signaling and prostate cancer
title_full Current perspectives on FOXA1 regulation of androgen receptor signaling and prostate cancer
title_fullStr Current perspectives on FOXA1 regulation of androgen receptor signaling and prostate cancer
title_full_unstemmed Current perspectives on FOXA1 regulation of androgen receptor signaling and prostate cancer
title_short Current perspectives on FOXA1 regulation of androgen receptor signaling and prostate cancer
title_sort current perspectives on foxa1 regulation of androgen receptor signaling and prostate cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4477823/
https://www.ncbi.nlm.nih.gov/pubmed/26114156
http://dx.doi.org/10.1016/j.gendis.2015.01.003
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