Androgen receptor corepressors: An overview

被引:87
作者
Wang, L
Hsu, CL
Chang, CS [1 ]
机构
[1] Univ Rochester, Med Ctr, George H Whipple Lab Canc Res, Dept Pathol, Rochester, NY 14642 USA
[2] Univ Rochester, Med Ctr, George H Whipple Lab Canc Res, Dept Urol, Rochester, NY 14642 USA
[3] Univ Rochester, Med Ctr, George H Whipple Lab Canc Res, Dept Radiat Oncol, Rochester, NY 14642 USA
[4] Chang Gung Mem Hosp, Dept Internal Med, Div Hematol Oncol, Taipei 10591, Taiwan
关键词
D O I
10.1002/pros.20170
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Androgens play pivotal roles in sex differentiation and development, in reproductive functions, and sexual behavior. The actions of androgens are mediated through the intracellular androgen receptor (AR), a member of the nuclear receptor (NR) superfamily, which regulates a wide range of target gene expression. Recent studies indicate that the proper transcriptional activity of AR is modulated by AR coregulators, including coactivators that can enhance AR transactivation and corepressors that can suppress AR transactivation. Here, we summarize the recent discoveries relating to AR corepressor function with the following different mechanisms: (1) corepressors that inhibit the DNA binding or nuclear translocation of AR; (2) corepressors that recruit histone deacetylases; (3) corepressors that interrupt the interaction between AR and its coactivators; (4) corepressors that interrupt the interaction between the N-terminus and C-terminus of AR; (5) corepressors that function as scaffolds for other AR coregulators; (6) corepressors that target the basal transcriptional machinery; (7) other mechanisms. The potential impact and future directions of AR corepressors are also discussed. (c) 2004 Wiley-Liss, Inc.
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页码:117 / 130
页数:14
相关论文
共 128 条
[1]   Repressors of androgen and progesterone receptor action [J].
Agoulnik, IU ;
Krause, WC ;
Bingman, WE ;
Rahman, HT ;
Amrikachi, M ;
Ayala, GE ;
Weigel, NL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (33) :31136-31148
[2]  
[Anonymous], 1995, Lancet, V346, P265
[3]   A novel homeobox protein which recognizes a TGT core and functionally interferes with a retinoid-responsive motif [J].
Bertolino, E ;
Reimund, B ;
WildtPerinic, D ;
Clerc, RG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (52) :31178-31188
[4]   Tip60 is a nuclear hormone receptor coactivator [J].
Brady, ME ;
Ozanne, DM ;
Gaughan, L ;
Waite, I ;
Cook, S ;
Neal, DE ;
Robson, CN .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (25) :17599-17604
[5]   MODULATION OF GENE-EXPRESSION BY CALRETICULIN BINDING TO THE GLUCOCORTICOID RECEPTOR [J].
BURNS, K ;
DUGGAN, B ;
ATKINSON, EA ;
FAMULSKI, KS ;
NEMER, M ;
BLEACKLEY, RC ;
MICHALAK, M .
NATURE, 1994, 367 (6462) :476-480
[6]  
Burris TP, 1996, RECENT PROG HORM RES, V51, P241
[7]  
Cairns P, 1997, CANCER RES, V57, P4997
[8]   New insights into tumor suppression: PTEN suppresses tumor formation by restraining the phosphoinositide 3-kinase AKT pathway [J].
Cantley, LC ;
Neel, BG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (08) :4240-4245
[9]   MOLECULAR-CLONING OF NEW HUMAN TR2 RECEPTORS - A CLASS OF STEROID-RECEPTOR WITH MULTIPLE LIGAND-BINDING DOMAINS [J].
CHANG, C ;
KOKONTIS, J ;
ACAKPOSATCHIVI, L ;
LIAO, S ;
TAKEDA, H ;
CHANG, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 165 (02) :735-741
[10]   STRUCTURAL-ANALYSIS OF COMPLEMENTARY-DNA AND AMINO-ACID SEQUENCES OF HUMAN AND RAT ANDROGEN RECEPTORS [J].
CHANG, CS ;
KOKONTIS, J ;
LIAO, SS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (19) :7211-7215