恩扎鲁胺
前列腺癌
雄激素受体
癌症研究
雅普1
心理压抑
化学
医学
癌症
内科学
基因表达
转录因子
生物化学
基因
作者
Eul Ju Seo,Byul A Jee,Jae Hoon Chung,Wan Song,Hyun Hwan Sung,Hwang Gyun Jeon,Byong Chang Jeong,Seong Il Seo,Seong Soo Jeon,Hyun Moo Lee,Minyong Kang
出处
期刊:FEBS Journal
[Wiley]
日期:2022-10-30
卷期号:290 (6): 1645-1662
被引量:2
摘要
Metastatic castration-resistant prostate cancer (mCRPC) is an aggressive and fatal disease, with most patients succumbing within 1–2 years despite undergoing multiple treatments. Androgen-receptor (AR) inhibitors, including enzalutamide (ENZ), are used for the treatment of mCRPC; however, most patients develop resistance to ENZ. Herein, we propose that the repression of SLC22A3 by AR-V7/YAP1/TAZ conferred ENZ resistance in mCRPC. SLC22A3 expression is specifically downregulated in the ENZ-resistant C4-2B MDVR cells, and when YAP1/TAZ is hyperactivated by AR full-length or AR-V7, these proteins interact with DNMT1 to repress SLC22A3 expression. We observed low SLC22A3 expression and high levels of TAZ or YAP1 in mCRPC patient tissues harbouring AR-V7 and the opposite expression patterns in normal patient tissues. Our findings suggest a mechanism underlying ENZ resistance by providing evidence that the AR-V7/YAP1/TAZ axis represses SLC22A3, which could be a potential treatment target in prostate cancer.
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