BRCA2 cooperates with histone acetyltransferases in androgen receptor-mediated transcription.

Abstract:

:Germ-line mutations of the BRCA2 tumor suppressor gene greatly increase the risk of developing breast and ovarian cancers. Here, we show that wild-type BRCA2, but not a tumor-specific truncated mutant BRCA2, synergizes with the nuclear receptor coactivator p160 GRIP1 to enhance transcriptional activation by androgen receptor (AR). BRCA2 not only associates with AR and GRIP1 but also cooperates with both the histone acetyltransferase P/CAF and BRCA1 to enhance AR- and GRIP1-mediated transactivation. As such, BRCA2 can exert its tumor suppressor function, in part, by modulating androgen signaling, which has been shown to be antiproliferative in a subset of breast cancer cells and particularly implicated in male breast tumors.

authors

Shin S,Verma IM

doi

10.1073/pnas.1132020100

keywords:

subject

Has Abstract

pub_date

2003-06-10 00:00:00

pages

7201-6

issue

12

eissn

0027-8424

issn

1091-6490

pii

1132020100

journal_volume

100

pub_type

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