The androgen receptor mRNA

被引:57
作者
Yeap, BB
Wilce, JA
Leedman, PJ
机构
[1] Univ Western Australia, Sch Med & Pharmacol, Nedlands, WA 6009, Australia
[2] Royal Perth Hosp, Perth, WA, Australia
[3] Univ Western Australia, Sch Biomed & Chem Sci, Nedlands, WA 6009, Australia
[4] Univ Western Australia, Lab Canc Med, Med Res Ctr, Nedlands, WA 6009, Australia
[5] Western Australian Inst Med Res, Perth, WA, Australia
关键词
D O I
10.1002/bies.20051
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Androgens (testosterone), acting via the androgen receptor (AR) a nuclear transcription factor, regulate male sexual development and body composition. In addition, AR expression plays an important role in the proliferation of human prostate cancer and confers a better prognosis in breast cancer. AR mRNA stability is central to the regulation of AR expression in prostate and breast cancer cells, and recent studies have demonstrated binding by members of the ELAV/Hu and poly(C) RNA-binding protein families to a highly conserved UC-rich element in the X-untranslated region of AR mRNA, with functional impact on AR protein expression. Remarkably, a CAG trinucleotide repeat in exon 1 of the AR, the length of which has been linked to prostate cancer survival, is also a target for multiple RNA-binding proteins from a variety of human and murine tissues. In this review, we will detail the current knowledge of the mechanisms involved in regulating AR mRNA stability, the nature, potential role and structural biology of several novel AR mRNA-protein interactions, and the implications for novel therapeutics in human prostate cancer. (C) 2004 Wiley Periodicals, Inc.
引用
收藏
页码:672 / 682
页数:11
相关论文
共 97 条
[61]   Cleavage, aggregation and toxicity of the expanded androgen receptor in spinal and bulbar muscular atrophy [J].
Merry, DE ;
Kobayashi, Y ;
Bailey, CK ;
Taye, AA ;
Fischbeck, KH .
HUMAN MOLECULAR GENETICS, 1998, 7 (04) :693-701
[62]   REDUCED TRANSCRIPTIONAL REGULATORY COMPETENCE OF THE ANDROGEN RECEPTOR IN X-LINKED SPINAL AND BULBAR MUSCULAR-ATROPHY [J].
MHATRE, AN ;
TRIFIRO, MA ;
KAUFMAN, M ;
KAZEMIESFARJANI, P ;
FIGLEWICZ, D ;
ROULEAU, G ;
PINSKY, L .
NATURE GENETICS, 1993, 5 (02) :184-188
[63]   The CAG trinucleotide repeat length in the androgen receptor does not predict the early onset of prostate cancer [J].
Mir, K ;
Edwards, J ;
Paterson, PJ ;
Hehir, M ;
Underwood, MA ;
Bartlett, JMS .
BJU INTERNATIONAL, 2002, 90 (06) :573-578
[64]   Androgen receptors frequently are expressed in breast carcinomas - Potential relevance to new therapeutic strategies [J].
Moinfar, F ;
Okcu, M ;
Tsybrovskyy, O ;
Regitnig, P ;
Lax, SF ;
Weybora, W ;
Ratschek, M ;
Tavassoli, FA ;
Denk, H .
CANCER, 2003, 98 (04) :703-711
[65]   Autoregulation of androgen receptor protein and messenger RNA in rat ventral prostate is protein synthesis dependent [J].
Mora, GR ;
Prins, GS ;
Mahesh, VB .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1996, 58 (5-6) :539-549
[66]   Poly(rC) binding proteins mediate poliovirus mRNA stability [J].
Murray, KE ;
Roberts, AW ;
Barton, DJ .
RNA, 2001, 7 (08) :1126-1141
[67]   Identification of HuR as a protein implicated in AUUUA-mediated mRNA decay [J].
Myer, VE ;
Fan, XHC ;
Steitz, JA .
EMBO JOURNAL, 1997, 16 (08) :2130-2139
[68]   FAMILIAL BULBO-SPINAL MUSCULAR-ATROPHY ASSOCIATED WITH TESTICULAR ATROPHY AND SENSORY NEUROPATHY (KENNEDY-ALTER-SUNG SYNDROME) - AUTOPSY CASE-REPORT OF 2 BROTHERS [J].
NAGASHIMA, T ;
SEKO, K ;
HIROSE, K ;
MANNEN, T ;
YOSHIMURA, S ;
ARIMA, R ;
NAGASHIMA, K ;
MORIMATSU, Y .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1988, 87 (2-3) :141-152
[69]   mRNA silencing in erythroid differentiation: hnRNP K and hnRNP E1 regulate 15-lipoxygenase translation from the 3' end [J].
Ostareck, DH ;
OstareckLederer, A ;
Wilm, M ;
Thiele, BJ ;
Mann, M ;
Hentze, MW .
CELL, 1997, 89 (04) :597-606
[70]   Regulation of tyrosine hydroxylase mRNA stability by protein-binding, pyrimidine-rich sequence in the 3′-untranslated region [J].
Paulding, WR ;
Czyzyk-Krzeska, MF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (04) :2532-2538