Home LiteratureArticle Details
PMID: 11328859 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Cyclin D1 binds the androgen receptor and regulates hormone-dependent signaling in a p300/CBP-associated factor (P/CAF)-dependent manner.

Molecular endocrinology (Baltimore, Md.) ·Vol. 15 ·No. 5 ·2001-05-00 ·Pages 797-811

Reutens AT, Fu M, Wang C, Albanese C, McPhaul MJ, Sun Z, Balk SP, Jänne OA, Palvimo JJ, Pestell RG

Abstract

The androgen receptor (AR) is a ligand-regulated member of the nuclear receptor superfamily. The cyclin D1 gene product, which encodes the regulatory subunit of holoenzymes that phosphorylate the retinoblastoma protein (pRB), promotes cellular proliferation and inhibits cellular differentiation in several different cell types. Herein the cyclin D1 gene product inhibited ligand-induced AR- enhancer function through a pRB-independent mechanism requiring the cyclin D1 carboxyl terminus. The histone acetyltransferase activity of P/CAF (p300/CBP associated factor) rescued cyclin D1-mediated AR trans-repression. Cyclin D1 and the AR both bound to similar domains of P/CAF, and cyclin D1 displaced binding of the AR to P/CAF in vitro. These studies suggest cyclin D1 binding to the AR may repress ligand-dependent AR activity by directly competing for P/CAF binding.

MeSH Terms
Acetyltransferases/antagonists & inhibitors,metabolism,physiology Amino Acid Sequence Androgen Receptor Antagonists Blotting, Western Cell Cycle Proteins/antagonists & inhibitors,metabolism,physiology Cyclin D1/metabolism,physiology Histone Acetyltransferases Humans Ligands Male Molecular Sequence Data Mutation Prostatic Neoplasms/metabolism Receptors, Androgen/metabolism,physiology Sequence Alignment Signal Transduction/physiology Transcription Factors Tumor Cells, Cultured p300-CBP Transcription Factors
Chemicals
Androgen Receptor Antagonists Cell Cycle Proteins Ligands Receptors, Androgen Transcription Factors Cyclin D1 Acetyltransferases Histone Acetyltransferases p300-CBP Transcription Factors p300-CBP-associated factor
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Reutens A T
The Albert Einstein Comprehensive Cancer Center, Division of Hormone-Dependent Tumor Biology, Department of Developmental and Molecular Biology Albert Einstein College of Medicine Bronx, New York 10461, USA.
Fu M
Wang C
Albanese C
McPhaul M J
Sun Z
Balk S P
Jänne O A
Palvimo J J
Pestell R G
Article Info
Journal
Molecular endocrinology (Baltimore, Md.)
Abbr.
Mol Endocrinol
ISSN
0888-8809
Published
2001-05-00
Pages
797-811
Language
English
Region
United States
NLM ID
8801431
Subset
IM
Grants
NCI NIH HHS · R01 CA070297-07 · United States
NCI NIH HHS · R01 CA070297-11A2 · United States
NIDDK NIH HHS · DK-03892 · United States
NIDDK NIH HHS · R01 DK061002-03 · United States
NCI NIH HHS · R01 CA070297 · United States
NCI NIH HHS · R01 CA087767-03 · United States
NCI NIH HHS · R01CA75503 · United States
NIDDK NIH HHS · R01 DK061002-04 · United States
NCI NIH HHS · R01 CA087767-02 · United States
NCI NIH HHS · R01 CA087767-05 · United States
NIDDK NIH HHS · R01 DK061002-05 · United States
NIDDK NIH HHS · R01 DK061002-01A1 · United States
NCI NIH HHS · R01CA70897 · United States
NCI NIH HHS · R01 CA087767-01A2 · United States
NCI NIH HHS · R01 CA087767 · United States
NIDDK NIH HHS · R01 DK061002 · United States
NCI NIH HHS · R01 CA087767-04 · United States
NCI NIH HHS · CA-70297 · United States
NCI NIH HHS · R01 CA070297-08 · United States
NCI NIH HHS · R01 CA070297-12 · United States
NIDDK NIH HHS · R01 DK061002-02 · United States
NCI NIH HHS · R01 CA070297-09 · United States
NCI NIH HHS · R01 CA070297-10 · United States
NCI NIH HHS · R01 CA070297-06A1 · United States
NCI NIH HHS · 5-P30-CA13330-26 · United States
Corrections
ErratumIn
-
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]