Knudsen Karen E, Scher Howard I
Departments of Cancer Biology, Urology, and Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Clin Cancer Res. 2009 Aug 1;15(15):4792-8. doi: 10.1158/1078-0432.CCR-08-2660. Epub 2009 Jul 28.
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.
临床数据和人类疾病模型表明,雄激素受体(AR)活性对于前列腺癌的发生、生长和进展至关重要。因此,前列腺腺癌在疾病各个阶段对AR信号传导的依赖性已被用于播散性肿瘤的治疗,其中AR功能的消除是一线治疗的目标。尽管这些策略最初是有效的,但复发性肿瘤会随着AR活性的恢复而出现,并且尚未找到持久的治疗方法来对抗疾病的这一阶段。对AR调节以及AR活性复苏背后机制的新见解为开发更有效抑制受体活性并延长至治疗失败过渡期的新策略提供了肥沃的土壤。