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微小RNA-372通过靶向胰岛素样生长因子2结合蛋白1抑制肾细胞癌的肿瘤增殖和侵袭。

miR-372 suppresses tumour proliferation and invasion by targeting IGF2BP1 in renal cell carcinoma.

作者信息

Huang Xuan, Huang Mingjie, Kong Lingbao, Li Yong

机构信息

The Institute of Translational Medicine, Nanchang University, Jiangxi, 330031, China.

College of Bioscience and Engineering, Jiangxi Agricultural University, Nanchang, Jiangxi, 330045, China.

出版信息

Cell Prolif. 2015 Oct;48(5):593-9. doi: 10.1111/cpr.12207.

Abstract

OBJECTIVES

MicroRNAs (miRNAs) are endogenous small non-coding RNAs that regulate proteins and mRNAs for degradation or translational suppression. Up to now, the role of miR-372 in renal cell carcinoma has remained unknown; in this study, we have aimed to reveal its functional importance in this tumour.

MATERIALS AND METHODS

qRT-PCR was performed to measure expression levels of miR-372 in renal cell carcinoma cell lines and tissues. CCK-8 and an invasion assay were performed to measure its functional role. Luciferase assays, qRT-PCR and western blotting were performed to discover miR-372's target gene.

RESULTS

We demonstrated that miRNA-372 was down-regulated in renal cell carcinoma cell lines and tissue specimens; its over-expression inhibited cell proliferation and invasion. Moreover, we showed that miRNA-372 repressed insulin-like growth factor 2 mRNA-binding protein 1 (IGF2BP1) expression by directly interacting with its putative binding site at the 3'-UTR. Furthermore, ectopic expression of IGF2BP1 significantly reversed suppression of cell proliferation and invasion caused by miR-372 over-expression.

CONCLUSIONS

Our data indicated that miR-372 seemed to function as a tumour suppressor in renal cell carcinoma progression by inhibiting the IGF2BP1 expression.

摘要

目的

微小RNA(miRNA)是内源性小非编码RNA,可调节蛋白质和mRNA以进行降解或翻译抑制。迄今为止,miR-372在肾细胞癌中的作用尚不清楚;在本研究中,我们旨在揭示其在该肿瘤中的功能重要性。

材料与方法

采用qRT-PCR检测肾癌细胞系和组织中miR-372的表达水平。进行CCK-8和侵袭试验以检测其功能作用。进行荧光素酶试验、qRT-PCR和蛋白质印迹法以发现miR-372的靶基因。

结果

我们证明miRNA-372在肾癌细胞系和组织标本中表达下调;其过表达抑制细胞增殖和侵袭。此外,我们表明miRNA-372通过直接与其3'-UTR上的假定结合位点相互作用来抑制胰岛素样生长因子2 mRNA结合蛋白1(IGF2BP1)的表达。此外,IGF2BP1的异位表达显著逆转了miR-372过表达引起的细胞增殖和侵袭抑制。

结论

我们的数据表明,miR-372似乎通过抑制IGF2BP1的表达在肾细胞癌进展中发挥肿瘤抑制作用。

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