AR-Signaling in Human Malignancies: Prostate Cancer and Beyond

被引:43
作者
Schweizer, Michael T. [1 ,2 ]
Yu, Evan Y. [1 ,2 ]
机构
[1] Univ Washington, Dept Med, Div Oncol, Seattle, WA 98109 USA
[2] Fred Hutchinson Canc Res Ctr, Seattle, WA 98109 USA
关键词
prostate cancer; breast cancer; bladder cancer; renal cell carcinoma; pancreatic cancer; ovarian cancer; hepatocellular cancer; endometrial cancer; androgen receptor; ANDROGEN RECEPTOR EXPRESSION; SALIVARY DUCT CARCINOMA; RENAL-CELL CARCINOMA; EPITHELIAL OVARIAN-CANCER; GROWTH-FACTOR RECEPTOR; HEPATOCELLULAR-CARCINOMA; BLADDER-CANCER; BREAST-CANCER; PHASE-II; ABIRATERONE ACETATE;
D O I
10.3390/cancers9010007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In the 1940s Charles Huggins reported remarkable palliative benefits following surgical castration in men with advanced prostate cancer, and since then the androgen receptor (AR) has remained the main therapeutic target in this disease. Over the past couple of decades, our understanding of AR-signaling biology has dramatically improved, and it has become apparent that the AR can modulate a number of other well-described oncogenic signaling pathways. Not surprisingly, mounting preclinical and epidemiologic data now supports a role for AR-signaling in promoting the growth and progression of several cancers other than prostate, and early phase clinical trials have documented preliminary signs of efficacy when AR-signaling inhibitors are used in several of these malignancies. In this article, we provide an overview of the evidence supporting the use of AR-directed therapies in prostate as well as other cancers, with an emphasis on the rationale for targeting AR-signaling across tumor types.
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页数:19
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