miR-202-5p inhibits the migration and invasion of osteosarcoma cells by targeting ROCK1

被引:27
|
作者
Li, Congda [1 ]
Ma, Deying [1 ]
Yang, Jinhu [1 ]
Lin, Xiangbo [1 ]
Chen, Bo [1 ]
机构
[1] Peoples Hosp Rizhao, Dept Orthoped, 126 Taian Rd, Rizhao 276800, Shandong, Peoples R China
关键词
miR-202-5p; invasion; migration; ROCK1; osteosarcoma; DOWN-REGULATING ROCK1; BREAST-CANCER CELLS; TUMOR-SUPPRESSOR; LUNG-CANCER; PROLIFERATION; PROGRESSION; METASTASIS; PROGNOSIS; CARCINOMA; EPIDEMIOLOGY;
D O I
10.3892/ol.2018.8694
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Many studies have shown that microRNA regulates the development and treatment of osteosarcoma (OS). In many human cancer studies, the expression of microRNA-202 has been shown to be abnormal. The aim of the study was to examine the role of miR-202-5p in the occurrence and formation of OS. miR-202-5p and Rho-associated coiled-coil containing protein kinase 1 (ROCK1) levels were assessed using RT-qPCR in OS tissues and cell lines. The cell migrating and invasive abilities were detected by the Transwell assay in OS. Moreover, the relationship between miR-202-5p and ROCK1 was verified via luciferase reporter assay. The protein level of ROCK1 was identified by western blot analysis. Downregulation of miR-202-5p was identified in OS tissues and cell lines. In addition, the miR-202-5p overexpression had inhibitory action for cell migration and invasion in OS. Moreover, miR-202-5p directly targeted ROCK1 and negatively regulated its expression. Upregulation of ROCK1 had a carcinogenic effect in OS. Furthermore, the upregulation of ROCK1 restored the suppressive effect of miR-202-5p. miR-202-5p, in turn, weakened the abilities of cell migration and invasion in OS by inhibiting ROCK1 expression. As a result, miR-202-5p may be developed as a potential pathway in the reatment of OS.
引用
收藏
页码:829 / 834
页数:6
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