Androgen receptor (AR) promotes clear cell renal cell carcinoma (ccRCC) migration and invasion via altering the circHIAT1/miR-195-5p/29a-3p/29c-3p/CDC42 signals

被引:168
|
作者
Wang, Kefeng [1 ]
Sun, Yin [2 ,3 ,4 ,5 ]
Tao, Wei [2 ,3 ,4 ,5 ]
Fei, Xiang [1 ]
Chang, Chawnshang [2 ,3 ,4 ,5 ,6 ]
机构
[1] China Med Univ, Shengjing Hosp, Dept Urol, Shenyang 110004, Peoples R China
[2] Univ Rochester, Med Ctr, Dept Pathol, George Whipple Lab Canc Res, Rochester, NY 14642 USA
[3] Univ Rochester, Med Ctr, Dept Urol, George Whipple Lab Canc Res, Rochester, NY 14642 USA
[4] Univ Rochester, Med Ctr, Dept Radiat Oncol, George Whipple Lab Canc Res, Rochester, NY 14642 USA
[5] Univ Rochester, Med Ctr, Wilmot Canc Ctr, Rochester, NY 14642 USA
[6] China Med Univ Hosp, Sex Hormone Res Ctr, Taichung 404, Taiwan
关键词
Androgen receptor; Renal cell carcinoma; Migration; Invasion; circRNA; CDC42; RESISTANT PROSTATE-CANCER; CIRCULAR RNAS; HEPATOCELLULAR-CARCINOMA; FILOPODIA FORMATION; EXPRESSION; CDC42; PROGRESSION; METASTASIS; ACTIVATION; SURVIVAL;
D O I
10.1016/j.canlet.2016.12.036
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Increasing evidence has demonstrated that the androgen receptor (AR) plays important roles to promote the metastasis of clear cell renal cell carcinoma (ccRCC). The detailed mechanisms, especially how AR functions via altering the circular RNAs (circRNAs) remain unclear. Here we identified a new circRNA (named as circHIAT1) whose expression was lower in ccRCCs than adjacent normal tissues. Targeting AR could suppress ccRCC cell progression via increasing circHIAT1 expression. ChIP assay and luciferase assay demonstrated that AR suppressed circHIAT1 expression via regulating its host gene, Hippocampus Abundant Transcript 1 (HIAT1) expression at the transcriptional level. The consequences of AR suppressed circHIAT1 resulted in deregulating miR-195-5p/29a-3p/29c-3p expressions, which increased CDC42 expression to enhance ccRCC cell migration and invasion. Increasing this newly identified signal via circHIAT1 suppressed AR-enhanced ccRCC cell migration and invasion. Together, these results suggested that circHIAT1 functioned as a metastatic inhibitor to suppress AR-enhanced ccRCC cell migration and invasion. Targeting this newly identified AR-circHIAT1-mediated miR-195-5p/29a-3p/29c-3p/CDC42 signals may help us develop potential new therapies to better suppress ccRCC metastasis. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 12
页数:12
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