Progression of prostate cancer: Multiple pathways to androgen independence

被引:107
作者
Devlin, Hong-Lin
Mudryj, Maria [1 ]
机构
[1] Univ Calif Davis, Sch Med, Dept Med Microbiol & Immunol, Davis, CA 95616 USA
关键词
Prostate cancer; Androgen receptor; Androgen independence; Calpain; Signaling; HORMONE-RECEPTOR COACTIVATOR; TUMOR-CELL LINES; CAG REPEAT; GENE-EXPRESSION; DEPRIVATION THERAPY; STEROID-BINDING; HINGE REGION; DNA-BINDING; GROWTH; ACTIVATION;
D O I
10.1016/j.canlet.2008.06.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Prostate cancer remains one of the most commonly diagnosed cancers and a leading cause of cancer death in men. Initially, prostate tumors respond to hormonal therapies. but androgen-independent tumors refractory to these therapies emerge. Identifying the mechanisms responsible for the emergence of androgen independence has been the subject of multiple studies. This article reviews the multiple pathways that have been shown to promote androgen independence, including a recently described mechanism that involves androgen receptor proteolysis to a constitutively active ligand-independent isoform. Identifying the underlying mechanisms of androgen independence is crucial in the design of appropriate therapies for hormonally refractive neoplasms. (C) 2009 Published by Elsevier Ireland Ltd.
引用
收藏
页码:177 / 186
页数:10
相关论文
共 99 条
[1]
Neuroendocrine cells in prostate cancer [J].
Amorino, GP ;
Parsons, SJ .
CRITICAL REVIEWS IN EUKARYOTIC GENE EXPRESSION, 2004, 14 (04) :287-300
[2]
AIB1, a steroid receptor coactivator amplified in breast and ovarian cancer [J].
Anzick, SL ;
Kononen, J ;
Walker, RL ;
Azorsa, DO ;
Tanner, MM ;
Guan, XY ;
Sauter, G ;
Kallioniemi, OP ;
Trent, JM ;
Meltzer, PS .
SCIENCE, 1997, 277 (5328) :965-968
[3]
Antiandrogens: selective androgen receptor modulators [J].
Berrevoets, CA ;
Umar, A ;
Brinkmann, AO .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2002, 198 (1-2) :97-103
[4]
BOLOGNA M, 1989, CANCER-AM CANCER SOC, V63, P1714
[5]
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
[6]
Constitutive activation of the androgen receptor by a point mutation in the hinge region:: A new mechanism for androgen-independent growth in prostate cancer [J].
Céraline, J ;
Cruchant, MD ;
Erdmann, E ;
Erbs, P ;
Kurtz, JE ;
Duclos, B ;
Jacqmin, D ;
Chopin, D ;
Bergerat, JP .
INTERNATIONAL JOURNAL OF CANCER, 2004, 108 (01) :152-157
[7]
Nuclear receptor coactivator ACTR is a novel histone acetyltransferase and forms a multimeric activation complex with P/CAF and CBP/p300 [J].
Chen, HW ;
Lin, RJ ;
Schiltz, RL ;
Chakravarti, D ;
Nash, A ;
Nagy, L ;
Privalsky, ML ;
Nakatani, Y ;
Evans, RM .
CELL, 1997, 90 (03) :569-580
[8]
Cerenkov line-like radiation and origin of iron Kα line in GRBs [J].
Chen, L ;
Liu, DB ;
Xu, YD ;
You, JH .
NEW ASTRONOMY, 2004, 10 (01) :39-52
[9]
Androgen receptor coregulators and their involvement in the development and progression of prostate cancer [J].
Chmelar, Renee ;
Buchanan, Grant ;
Need, Eleanor F. ;
Tilley, Wayne ;
Greenberg, Norman M. .
INTERNATIONAL JOURNAL OF CANCER, 2007, 120 (04) :719-733
[10]
NUCLEAR-LOCALIZATION OF ANDROGEN RECEPTOR IN HETEROGENEOUS SAMPLES OF NORMAL, HYPERPLASTIC AND NEOPLASTIC HUMAN PROSTATE [J].
CHODAK, GW ;
KRANC, DM ;
PUY, LA ;
TAKEDA, H ;
JOHNSON, K ;
CHANG, C .
JOURNAL OF UROLOGY, 1992, 147 (03) :798-803