Molecular regulation of androgen action in prostate cancer

被引:238
作者
Dehm, Scott M.
Tindall, Donald J.
机构
[1] Mayo Clin, Coll Med, Dept Urol, Rochester, MN 55905 USA
[2] Mayo Clin, Coll Med, Dept Biochem & Mol Biol, Rochester, MN 55905 USA
关键词
androgen receptor; prostate cancer; gene expression; transcription;
D O I
10.1002/jcb.20794
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 are critical regulators of prostate differentiation and function, as well as prostate cancer growth and survival. Therefore, androgen ablation is the preferred systemic treatment for disseminated prostate cancer. Androgen action is exerted in target tissues via binding the androgen receptor (AR), a nuclear receptor transcription factor. Historically, the gene expression program mediated by the AR has been poorly understood. However, recent gene expression profiling and more traditional single-gene characterization studies have revealed many androgen-regulated genes that are important mediators of androgen action in both normal and malignant prostate tissue. This review will focus on the androgen-regulated gene expression program, and examine how recently identified androgen-regulated genes are likely to contribute to the development and progression of prostate cancer. We will also summarize several recent studies that have attempted to unravel how these genes are deregulated in androgen depletion independent prostate cancer.
引用
收藏
页码:333 / 344
页数:12
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