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Tumor-suppressing effects of microRNA-429 in human renal cell carcinoma via the downregulation of Sp1

机译:MicroRNA-429通过下调Sp1在人肾细胞癌中的抑癌作用

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摘要

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.
机译:MicroRNA(miR)-429经常被报道在各种肿瘤中被下调,包括肾细胞癌(RCC),鼻咽癌,艾氏腹水肿瘤细胞,胃癌,非小细胞肺癌和子宫内膜子宫内膜样癌。本研究调查了miR-429对人RCC A498和786-O细胞的影响。用miR-429模拟物转染细胞并加扰对照后,进行MTT,细胞迁移,细胞侵袭和荧光素酶测定。此外,进行了蛋白质印迹分析以评估特异性蛋白1(Sp1)的表达,该蛋白被TargetScan预测为miR-429的靶标。目前的结果表明,miR-429抑制了786-O和A498细胞的增殖,迁移和侵袭。此外,目前的结果证明miR-429过表达下调了Sp1蛋白的表达,这提供了miR-429可能直接靶向RCC中Sp1的证据。这些结果表明,可以研究miR-429用作早期发现肿瘤转移和阻止RCC细胞侵袭的预测标志物。

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