| Literature DB >> 27698878 |
Deyao Wu1, Xiaobing Niu2, Huixing Pan1, Yunfeng Zhou1, Zichun Zhang1, Ping Qu1, Jian Zhou1.
Abstract
MicroRNA (miR)-429 has been frequently reported to be downregulated in various tumors, including renal cell carcinoma (RCC), nasopharyngeal carcinoma, Ehrlich ascites tumor cells, gastric cancer, non-small cell lung cancer and endometrial endometrioid carcinoma. The present study investigated the effects of miR-429 on human RCC A498 and 786-O cells. Following transfection of cells with miR-429 mimics and scrambled control, MTT, cell migration, cell invasion and luciferase assays were performed. In addition, western blotting was performed in order to assess the expression of specificity protein 1 (Sp1), which was predicted to be a target of miR-429 by TargetScan. The present results revealed that miR-429 inhibited cell proliferation, migration and invasion of 786-O and A498 cells. In addition, the present results demonstrated that miR-429 overexpression downregulated Sp1 protein expression, which provides evidence that miR-429 may directly target Sp1 in RCC. These results suggest that miR-429 may be investigated for use as a predictive marker for early detection of tumor metastasis and blocking RCC cells from becoming invasive.Entities:
Keywords: Sp1 miR-429; renal cell carcinoma
Year: 2016 PMID: 27698878 PMCID: PMC5038608 DOI: 10.3892/ol.2016.4953
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967