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首页> 外文期刊>Cancer biotherapy and radiopharmaceuticals >miR-5195-3p Suppresses Cell Proliferation and Induces Apoptosis by Directly Targeting NEDD9 in Osteosarcoma
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miR-5195-3p Suppresses Cell Proliferation and Induces Apoptosis by Directly Targeting NEDD9 in Osteosarcoma

机译:miR-5195-3p抑制细胞增殖,并通过直接靶向NEDD9在骨肉瘤中诱导细胞凋亡

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Objective: Aberrantly expressed microRNAs (miRs) have associated with the development and progression of osteosarcoma (OS). In this study, the authors aimed to investigate the biological function of miR-5195-3p and the underlying mechanisms. Methods: Quantitative real-time polymerase chain reaction analysis was performed to determine the expression of miR-5195-3p in OS tissues and cell lines. Then, two OS cell lines (MG-63 and U2OS) were transfected with miR-5195-3p mimics to obtain stably miR-5195-3p overexpression cell lines. A series of functional assays, including Cell Counting Kit-8 assay, colony formation assay, flow cytometry assay, and Hoechst staining were performed to analyze cell proliferation and apoptosis. Results: The authors first observed downregulation of miR-5195-3p in OS tissues and cell lines. A series of functional assays demonstrated that miR-5195-3p overexpression significantly attenuated OS cell proliferative activity and induced apoptosis. At a molecular level, the neural precursor cell which expressed developmentally downregulated protein 9 (NEDD9), was inversely correlated with the expression level of miR-5195-3p. Furthermore, ectopic expression of NEDD9 counteracted the antiproliferative and apoptotic effects of miR-5195-3p overexpression in OS cells. Conclusions: In summary, the miR-5195-3p/NEDD9 axis may be a promising antitumor agent for OS.
机译:目的:异常表达的MicroRNA(MIRS)与骨肉瘤(OS)的发育和进展有关。在这项研究中,作者旨在调查miR-5195-3P的生物学功能和潜在机制。方法:进行定量实时聚合酶链反应分析,以确定OS组织和细胞系中miR-5195-3P的表达。然后,用miR-5195-3p模拟物转染两个OS细胞系(Mg-63和U2OS),以获得稳定的miR-5195-3p过表达细胞系。进行一系列功能测定,包括细胞计数试剂盒测定,菌落形成测定,流式细胞术测定和Hoechst染色,以分析细胞增殖和凋亡。结果:作者首先在OS组织和细胞系中观察到miR-5195-3p的下调。一系列功能测定证明了MIR-5195-3P过表达显着减弱了OS细胞增殖活性和诱导的细胞凋亡。在分子水平下,表达显影下调蛋白质9(NEDD9)的神经前体细胞与miR-5195-3p的表达水平同时相关。此外,NEDD9的异位表达抵消了MIR-5195-3P过表达在OS细胞中的抗增殖和凋亡作用。结论:总之,MIR-5195-3P / NEDD9轴可以是OS的有希望的抗肿瘤剂。

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