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Metformin mediated microRNA-7 upregulation inhibits growth, migration, and invasion of non-small cell lung cancer A549 cells

机译:二甲双胍介导的MicroRNA-7上调抑制非小细胞肺癌A549细胞的生长,迁移和侵袭

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Metformin, a medication widely used in the treatment of type 2 diabetes mellitus, has a possible antitumor effect in type 2 diabetes mellitus patients. MicroRNA-7 is a significant microRNA in non-small cell lung cancer. Metformin has an inhibitory effect on lung cancer and regulates the expression of certain microRNAs, but there is no report connecting metformin with microRNA-7 in lung cancer. Thus, we used qPCR to measure microRNA-7 expression in A549 non-small cell lung cancer cells treated with metformin. We used CCK8, cell scratch, and Transwell assays to test the growth, migration, and invasion of A549 cells. Western blotting was used to measure the expression level of relevant proteins in A549 cells. We found that microRNA-7 was dramatically upregulated by metformin via AMPK in a dose- and time-dependent manner. Both metformin and microRNA-7 mimic reduced A549 cell growth, migration, and invasion. Metformin downregulated the levels of p-NF-κB p65, p-Erk1/2, p-AKT, and p-mTOR proteins. The treatment with the microRNA-7 mimic had the same result. The decrease of these proteins caused the inhibition of A549 cell growth, migration, and invasion. Our discovery revealed that metformin, via increasing the expression of microRNA-7 mediated by AMPK, regulates the AKT/mTOR, MAPK/Erk, and NF-κB signaling pathways, thereby suppressing A549 cell growth, migration, and invasion.
机译:二甲双胍,广泛用于治疗2型糖尿病的药物,在2型糖尿病患者中具有可能的抗肿瘤作用。 MicroRNA-7是非小细胞肺癌中的显着的微小RORNA。二甲双胍对肺癌具有抑制作用,并调节某些微小稻草的表达,但没有报告肺癌中的MicroRNA-7与microRNA-7连接。因此,我们使用QPCR测量用二甲双胍处理的A549非小细胞肺癌细胞中的MicroRNA-7表达。我们使用CCK8,Cell Scratch和Transwell测定来测试A549细胞的生长,迁移和侵袭。用于测量A549细胞中相关蛋白的表达水平的蛋白质印迹。我们发现MicroRNA-7通过Metformin通过AMPK以剂量和时间依赖的方式显着地上调。二甲双胍和MicroRNA-7两者都模仿A549细胞生长,迁移和侵袭。二甲双胍下调P-NF-κBP65,P-ERK1 / 2,P-AKT和P-MTOR蛋白水平。用microRNA-7模仿的处理具有相同的结果。这些蛋白质的降低导致抑制A549细胞生长,迁移和侵袭。我们的发现显示,通过增加由AMPK介导的microRNA-7的表达来调节Akt / mTOR,MAPK / ERK和NF-κB信号传导途径,从而抑制A549细胞生长,迁移和侵袭。

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    《Anti-cancer drugs 》 |2020年第4期| 共8页
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