首页> 美国卫生研究院文献>BMC Pulmonary Medicine >LINC02418 promotes malignant behaviors in lung adenocarcinoma cells by sponging miR-4677-3p to upregulate KNL1 expression
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LINC02418 promotes malignant behaviors in lung adenocarcinoma cells by sponging miR-4677-3p to upregulate KNL1 expression

机译:LINC02418通过海绵MIR-4677-3P促进肺腺癌细胞中的恶性行为来上调KNL1表达

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摘要

The biological function of LINC02418 in LAD. a Heatmap showing highly expressed LINC02418 in LAD. b LINC02418 expression in LAD cell lines and normal pulmonary epithelial cell line was examined by RT-qPCR. c The transfection efficiency of sh-LINC02418#1 and sh-LINC02418#2 in A549 and SPC-A1 cells were measured by RT-qPCR. d CCK-8 assay was performed to assess cell proliferation of A549 and SPC-A1 cells after the knockdown of LINC02418. e Colony formation assay was carried out to detect the proliferation of A549 and SPC-A1 cells in response to LINC02418 knockdown. f Transwell assay was applied to access cell migration in A549 and SPC-A1 cells after downregulation LINC02418. g Western blot was used to examine the level of migration-related proteins after knocking down LINC02418. **P < 0.01
机译:LINC02418在LAD中的生物学功能。在LAD中显示高表达的LINC02418的热图。通过RT-QPCR检测LAD细胞系和正常肺上皮细胞系中的LINC02418表达。 C通过RT-QPCR测量A549和SPC-A1细胞中SH-LINC02418#1和SH-LINC02418#2的转染效率。 DCK-8测定进行以评估LINC02418敲低后A549和SPC-A1细胞的细胞增殖。进行C菌落形成测定以检测A549和SPC-A1细胞的增殖,响应LINC02418敲低。 F Transwell测定被施用于在下调LINC02418后A549和SPC-A1细胞中的接入细胞迁移。 G Western印迹用于击落LINC02418后检查迁移相关蛋白水平。 ** p <0.01

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