TXNIP公司
癌症研究
下调和上调
生物
肾细胞癌
体内
转移
基因敲除
细胞生长
癌症
医学
病理
基因
生物化学
遗传学
生物技术
硫氧还蛋白
作者
Qiong Chen,Tao Liu,Yi Bao,Tangliang Zhao,Jie Wang,Hui Wang,Anbang Wang,Xinxin Gan,Zhenjie Wu,Linhui Wang
出处
期刊:Cancer Letters
[Elsevier BV]
日期:2019-10-17
卷期号:469: 68-77
被引量:162
标识
DOI:10.1016/j.canlet.2019.10.017
摘要
Circular RNAs (circRNAs) are reported to act as important regulators in cancers. CircRNA RAPGEF5 (cRAPGEF5) is derived from exons 2–6 of the RAPGEF5 gene and may promote papillary thyroid cancer progression. However, the role of cRAPGEF5 in renal cell carcinoma (RCC) remains unclear. In this study, we found cRAPGEF5 to be significantly downregulated in RCC tissues. Among 245 RCC cases, cRAPGEF5 downregulation correlated positively with aggressive clinical characteristics and independently predicted poor overall survival and recurrence-free survival. Functional assays demonstrated that cRAPGEF5 suppresses RCC proliferation and migration in vitro and in vivo. Mechanistically, RNA Immunoprecipitation and circRNA in vivo precipitation assays showed that cRAPGEF5 functions as a sponge of oncogenic miR-27a-3p, which targets the suppressor gene TXNIP. Interactions between miR-27a-3p and cRAPGEF5 or TXNIP were confirmed by dual-luciferase reporter assays. In conclusion, cRAPGEF5 plays a role in suppressing RCC via the miR-27a-3p/TXNIP pathway and may serve as a promising prognostic biomarker and novel therapeutic target for RCC patients.
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