4.7 Article

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

Journal

CLINICAL CANCER RESEARCH
Volume 15, Issue 15, Pages 4792-4798

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1078-0432.CCR-08-2660

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Funding

  1. NCI NIH HHS [R01 CA116777-04, R01 CA099996, R01 CA099996-07A2, R01 CA116777] Funding Source: Medline
  2. NIEHS NIH HHS [R01 ES016675, R01 ES016675-10] Funding Source: Medline

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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.

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