雄激素受体
癌症研究
肾细胞癌
癌症
肿瘤进展
生物
医学
内科学
前列腺癌
遗传学
作者
Dalin He,Lei Li,Guodong Zhu,Liang Liang,Zhenfeng Guan,Luke S. Chang,Yuan Chen,Shuyuan Yeh,Chawnshang Chang
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2014-06-13
卷期号:74 (16): 4420-4430
被引量:89
标识
DOI:10.1158/0008-5472.can-13-2681
摘要
Abstract Males have a higher incidence of renal cell carcinoma (RCC) than females, but the reason for this gender difference is unknown. Addressing this question, we report the discovery of an androgen receptor (AR)–induced HIF2α/VEGF signal that drives RCC progression. AR attenuation or augmentation in RCC cells altered their proliferation, migration, and invasion in multiple models in vitro and in vivo. Mechanistic investigations revealed that AR targeting inhibited RCC cell migration and invasion by modulating HIF2α/VEGF signals at the level of mRNA and protein expression. Interrupting HIF2α/VEGF signals with inhibitors of either HIF2α or VEGF was sufficient to suppress RCC progression. Similarly, the specific AR degradation enhancer ASC-J9 was sufficient to suppress AR-induced HIF2α/VEGF signaling and RCC progression in multiple models in vitro and in vivo. Taken together, our results revealed a novel role for AR in RCC initiation and progression with implications for novel therapeutic strategies. Cancer Res; 74(16); 4420–30. ©2014 AACR.
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