The androgen receptor in hormone-refractory prostate cancer

被引:12
作者
Mao, Hai-Lei [1 ,2 ]
Zhu, Zhi-Qi [1 ]
Chen, Charlie Degui [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Biochem & Cell Biol, Shanghai Key Lab Androl,State Key Lab Mol Biol, Shanghai 200031, Peoples R China
[2] Nantong Univ, Affiliated Hosp, Nantong 226001, Peoples R China
基金
中国国家自然科学基金;
关键词
prostate cancer; hormone therapy; androgen receptor; hormone-refractory prostate cancer; STEROID BINDING CHARACTERISTICS; GROWTH-FACTOR-I; INCREASED EXPRESSION; CELLS; GENE; AMPLIFICATION; ACTIVATION; CARCINOMA; MUTATION; THERAPY;
D O I
10.1038/aja.2008.14
中图分类号
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
摘要
Advanced prostate cancer is responsive to hormone therapy that interferes with androgen receptor (AR) signalling. However, the effect is short-lived, as nearly all tumours progress to a hormone-refractory (HR) state, a lethal stage of the disease. Intuitively, the AR should not be involved because hormone therapy that blocks or reduces AR activity is not effective in treating HR tumours. However, there is still a consensus that AR plays an essential role in HR prostate cancer (HRPC) because AR signalling is still functional in HR tumours. AR signalling can be activated in HR tumours through several mechanisms. First, activation of intracellular signal transduction pathways can sensitize the AR to castrate levels of androgens. Also, mutations in the AR can change AR ligand specificity, thereby allowing it to be activated by non-steroids or anti-androgens. Finally, overexpression of the wild-type AR sensitizes itself to low concentrations of androgens. Therefore, drugs targeting AR signalling could still be effective in treating HRPC.
引用
收藏
页码:68 / 73
页数:5
相关论文
共 27 条
[21]  
Taplin ME, 1999, CANCER RES, V59, P2511
[22]   MUTATION OF THE ANDROGEN-RECEPTOR GENE IN METASTATIC ANDROGEN-INDEPENDENT PROSTATE-CANCER [J].
TAPLIN, ME ;
BUBLEY, GJ ;
SHUSTER, TD ;
FRANTZ, ME ;
SPOONER, AE ;
OGATA, GK ;
KEER, HN ;
BALK, SP .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (21) :1393-1398
[23]   Testosterone and dihydrotestosterone tissue levels in recurrent prostate cancer [J].
Titus, MA ;
Schell, MJ ;
Lih, FB ;
Tomer, KB ;
Mohler, JL .
CLINICAL CANCER RESEARCH, 2005, 11 (13) :4653-4657
[24]   A MUTATION IN THE LIGAND-BINDING DOMAIN OF THE ANDROGEN RECEPTOR OF HUMAN LNCAP CELLS AFFECTS STEROID BINDING CHARACTERISTICS AND RESPONSE TO ANTI-ANDROGENS [J].
VELDSCHOLTE, J ;
RISSTALPERS, C ;
KUIPER, GGJM ;
JENSTER, G ;
BERREVOETS, C ;
CLAASSEN, E ;
VANROOIJ, HCJ ;
TRAPMAN, J ;
BRINKMANN, AO ;
MULDER, E .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 173 (02) :534-540
[25]   THE ANDROGEN RECEPTOR IN LNCAP CELLS CONTAINS A MUTATION IN THE LIGAND-BINDING DOMAIN WHICH AFFECTS STEROID BINDING CHARACTERISTICS AND RESPONSE TO ANTIANDROGENS [J].
VELDSCHOLTE, J ;
BERREVOETS, CA ;
RISSTALPERS, C ;
KUIPER, GGJM ;
JENSTER, G ;
TRAPMAN, J ;
BRINKMANN, AO ;
MULDER, E .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1992, 41 (3-8) :665-669
[26]   IN-VIVO AMPLIFICATION OF THE ANDROGEN RECEPTOR GENE AND PROGRESSION OF HUMAN PROSTATE-CANCER [J].
VISAKORPI, T ;
HYYTINEN, E ;
KOIVISTO, P ;
TANNER, M ;
KEINANEN, R ;
PALMBERG, C ;
PALOTIE, A ;
TAMMELA, T ;
ISOLA, J ;
KALLIONIEMI, OP .
NATURE GENETICS, 1995, 9 (04) :401-406
[27]   Glucocorticoids can promote androgen-independent growth of prostate cancer cells through a mutated androgen receptor [J].
Zhao, XY ;
Malloy, PJ ;
Krishnan, AV ;
Swami, S ;
Navone, NM ;
Peehl, DM ;
Feldman, D .
NATURE MEDICINE, 2000, 6 (06) :703-706