Antiandrogens: selective androgen receptor modulators

被引:58
作者
Berrevoets, CA [1 ]
Umar, A [1 ]
Brinkmann, AO [1 ]
机构
[1] Erasmus Univ, Med Ctr Rotterdam, Dept Reprod & Dev, NL-3000 DR Rotterdam, Netherlands
关键词
androgens; antiandrogens; androgen receptor; N-CoR;
D O I
10.1016/S0303-7207(02)00373-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Antiandrogens can efficiently block androgen receptor (AR) mediated gene expression, and are therefore useful tools in the treatment of androgen dependent prostate cancer. Antiandrogens are either complete or partial inhibitors of AR activity, depending on the nature of the compound. As compared to androgens, antiandrogens induce a different AR conformation, thereby influencing the recruitment of co-regulators (coactivators and corepressors). This ligand-selective modulation of AR activty is affected by an AR mutation (Thr877Ala substitution) found in prostate cancer. In contrast to the wild-type AR, the mutant AR conformation induced by cyproterone acetate (CPA) and hydroxyflutamide (OHF) is comparable to that induced by androgens. As a consequence, this might affect recruitment of co-regulators, thereby allowing CPA and OHF to act as strong agonists on the mutant AR. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:97 / 103
页数:7
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