Starving the Addiction: New Opportunities for Durable Suppression of AR Signaling in Prostate Cancer

被引:242
作者
Knudsen, Karen E. [1 ,2 ,3 ]
Scher, Howard I. [4 ,5 ]
机构
[1] Thomas Jefferson Univ, Kimmel Canc Ctr, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Dept Canc Biol, Philadelphia, PA 19107 USA
[3] Thomas Jefferson Univ, Dept Urol, Philadelphia, PA 19107 USA
[4] Mem Sloan Kettering Canc Ctr, Genitourinary Oncol Serv, Dept Med, Sidney Kimmel Ctr Prostate & Urol Cancers, New York, NY 10021 USA
[5] Cornell Univ, Joan & Sanford E Weill Coll Med, Dept Med, New York, NY 10021 USA
关键词
INITIAL HORMONAL MANAGEMENT; ANDROGEN-RECEPTOR; ABIRATERONE ACETATE; THERAPY RESISTANCE; AMERICAN-SOCIETY; NUCLEAR RECEPTOR; GNRH ANTAGONISTS; CASTRATION; PROGRESSION; MECHANISMS;
D O I
10.1158/1078-0432.CCR-08-2660
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Clinical data and models of human disease indicate that androgen receptor (AR) activity is essential for prostate cancer development, growth, and progression. The dependence of prostatic adenocarcinoma on AR signaling at all stages of disease has thereby been exploited in the treatment of disseminated tumors, for which ablation of AR function is the goal of first-line therapy. Although these strategies are initially effective, recurrent tumors arise with restored AR activity, and no durable treatment has yet been identified to combat this stage of disease. New insights into AR regulation and the mechanisms underlying resurgent AR activity have provided fertile ground for the development of novel strategies to more effectively inhibit receptor activity and prolong the transition to therapeutic failure.
引用
收藏
页码:4792 / 4798
页数:7
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