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miR-494 inhibits ovarian cancer cell proliferation and promotes apoptosis by targeting FGFR2

机译:miR-494通过靶向FGFR2抑制卵巢癌细胞增殖并促进凋亡

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摘要

MicroRNAs (miRs) have been reported to be key regulators in numerous types of cancer. The aim of the present study was to investigate the role of miR-494 in ovarian cancer. Expression of miR-494 was analyzed in ovarian cancer tissues and cell lines by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). miR-494 mimic or negative control was transiently transfected into A2780 and SKOV3 cell lines. A cell counting kit-8 assay was performed to assess the effects of miR-494 on cell proliferation, and flow cytometry was used to evaluate the apoptotic rate. The target gene of miR-494 was detected by luciferase assay. Expression of fibroblast growth factor receptor 2 (FGFR2) was identified using RT-qPCR and western blotting. In the present study, decreased expression of miR-494 was observed in ovarian cancer samples and cell lines. Overexpression of miR-494 inhibited ovarian cancer cell proliferation by inducing apoptosis. Additional investigation indicated that FGFR2 was a direct target of miR-494. Taken together, the results of the present study suggested that miR-494 suppressed ovarian cancer cell proliferation by inducing apoptosis via targeting FGFR2.
机译:据报道,MicroRNA(miRs)是多种类型癌症的关键调控因子。本研究的目的是研究miR-494在卵巢癌中的作用。通过逆转录定量聚合酶链反应(RT-qPCR)分析了miR-494在卵巢癌组织和细胞系中的表达。将miR-494模拟或阴性对照瞬时转染到A2780和SKOV3细胞系中。进行了细胞计数试剂盒8分析,以评估miR-494对细胞增殖的影响,并使用流式细胞仪评估细胞凋亡率。通过荧光素酶测定法检测miR-494的靶基因。使用RT-qPCR和Western blotting鉴定成纤维细胞生长因子受体2(FGFR2)的表达。在本研究中,在卵巢癌样品和细胞系中观察到miR-494的表达降低。 miR-494的过表达通过诱导细胞凋亡来抑制卵巢癌细胞的增殖。进一步的研究表明,FGFR2是miR-494的直接靶标。两者合计,本研究的结果表明miR-494通过靶向FGFR2诱导凋亡来抑制卵巢癌细胞的增殖。

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