The effect of miR-124-3p on cell proliferation and apoptosis in bladder cancer by targeting EDNRB

Weijin Fu, Xiaoyun Wu, Zhanbin Yang, Hua Mi
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引用次数: 34

Abstract

Introduction Endothelin receptor type B (EDNRB) is a potential target gene of miR-124-3p, but the association between miR-124-3p and EDNRB has not yet been reported. The aim of this study was to investigate the role of miR-124-3p in bladder cancer (BC) and to determine whether miR-124-3p regulates cell proliferation by targeting EDNRB. Material and methods Bladder cancer tissues and cell lines were obtained in order to analyze the miR-124-3p and EDNRB expression through quantitative RT-PCR (qRT-PCR) and western blotting analysis. The dual-luciferase reporter assay was employed to confirm the relationship between miR-124-3p and EDNRB. The manipulation of miR-124-3p and EDNRB expression was achieved through cell transfection. Cell proliferation and apoptosis were evaluated by MTS assay, colony forming assay and flow cytometry. A nude mouse tumorigenicity assay was used to detect the effects of miR-124-3p in vivo. Results There was an inverse correlation between the expression of miR-124-3p and EDNRB; miR-124-3p was down-regulated and EDNRB was up-regulated in BC tissues and cell lines. MiR-124-3p was observed to target EDNRB and suppress its expression. Other studies have suggested that the transfection of miR-124-3p mimics and EDNRB siRNA can suppress BC cell proliferation and induce cell apoptosis. Conclusions miR-124-3p regulates the proliferation and apoptosis of BC cells by suppressing EDNRB expression.
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miR-124-3p靶向EDNRB对膀胱癌细胞增殖和凋亡的影响
内皮素受体B型(EDNRB)是miR-124-3p的潜在靶基因,但miR-124-3p与EDNRB之间的关联尚未见报道。本研究的目的是探讨miR-124-3p在膀胱癌(BC)中的作用,并确定miR-124-3p是否通过靶向EDNRB调控细胞增殖。材料和方法获取膀胱癌组织和细胞系,通过定量RT-PCR (qRT-PCR)和western blotting分析miR-124-3p和EDNRB的表达。采用双荧光素酶报告基因检测来证实miR-124-3p与EDNRB之间的关系。通过细胞转染实现对miR-124-3p和EDNRB表达的操纵。采用MTS法、集落形成法和流式细胞术观察细胞增殖和凋亡情况。采用裸鼠致瘤性实验检测miR-124-3p在体内的作用。结果miR-124-3p与EDNRB表达呈负相关;在BC组织和细胞系中miR-124-3p下调,EDNRB上调。观察到MiR-124-3p靶向EDNRB并抑制其表达。其他研究表明,转染miR-124-3p模拟物和EDNRB siRNA可抑制BC细胞增殖并诱导细胞凋亡。结论miR-124-3p通过抑制EDNRB的表达调控BC细胞的增殖和凋亡。
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