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首页> 外文期刊>Molecular Genetics & Genomic Medicine >miR‐584‐5p regulates hepatocellular carcinoma cell migration and invasion through targeting KCNE2
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miR‐584‐5p regulates hepatocellular carcinoma cell migration and invasion through targeting KCNE2

机译:miR-584-5p通过靶向kcne2调节肝细胞癌细胞迁移和侵袭

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Background Hepatocellular carcinoma (HCC) is one of the most commonly diagnosed cancer type. This study was aimed to investigate the role of microRNA‐584‐5p ( miR‐584‐5p ) in regulating HCC progression. Methods The expression of miR‐584‐5p in HCC cell lines was analyzed by quantitative?real‐time polymerase chain reaction. Effects of miR‐584‐5p depletion on HCC cell proliferation, migration, and invasion in vitro were analyzed by cell counting kit‐8 assay, wound‐healing assay, and transwell invasion assay. miR‐584‐5p targeting potassium voltage‐gated channel subfamily E regulatory subunit 2 ( KCNE2 ) was identified using bioinformatics algorithm and dual‐luciferase activity reporter assay. Kaplan–Meier Plotter website was used to investigate the effect of miR‐584‐5p or KCNE2 expression on the overall survival of HCC patients. Results In vitro functional assays showed miR‐584‐5p depletion decreased HCC cell proliferation, cell migration, and cell invasion. Moreover, miR‐584‐5p functions by directly targeting KCNE2 , and it in turn, mediates the effects of miR‐584‐5p on HCC cell behaviors. Conclusions These results demonstrated that miR‐584‐5p functions as an oncogenic miRNA in HCC.
机译:背景技术肝细胞癌(HCC)是最常见的癌症类型之一。本研究旨在调查MicroRNA-584-5P(miR-584-5P)在调节HCC进展方面的作用。方法通过定量α分析HCC细胞系MIR-584-5P在HCC细胞系中的表达。实时聚合酶链反应。 MiR-584-5P耗尽对HCC细胞增殖,迁移和侵袭的影响,通过细胞计数试剂盒 - 8测定,伤口愈合测定和Transwell Invasion测定分析。使用生物信息学算法和双荧光素酶活性报告分析来鉴定MiR-584-5P靶向钾电压门通道亚家族E调节亚基2(KCNE2)。 Kaplan-Meier绘图仪网站用于探讨miR-584-5p或kcne2表达对HCC患者整体存活的影响。结果在体外功能测定显示MIR-584-5P耗尽降低了HCC细胞增殖,细胞迁移和细胞侵袭。此外,MiR-584-5P通过直接靶向KCNE2,反过来介绍MIR-584-5P对HCC细胞行为的影响。结论这些结果表明miR-584-5p作为HCC中的致癌物质。

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