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MiR-187 suppresses non-small-cell lung cancer cell proliferation by targeting FGF9

机译:MiR-187通过靶向FGF9抑制非小细胞肺癌细胞增殖

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摘要

Non-small-cell lung cancer (NSCLC) is the main pathological type of lung cancer and has a low overall five-year survival rate. miR-187 has been reported to play major roles in various tumor types. In this study, we explored the impact of miR-187 on NSCLC. qRT-PCR results demonstrated that miR-187 expression is lower in NSCLC and cancer cells than normal tissues and normal lung cells. miR-187 expression levels are associated with tumor size, TNM stage and overall survival rate. MTS and colony formation assays showed that high miR-187 expression inhibits NSCLC cell proliferation and colony formation ability, and flow cytometry showed that miR-187 overexpression induces cell cycle arrest at the G0/G1 phase. A luciferase reporter assay showed that FGF9 is a target of miR-187. miR-187 overexpression reduces the expression of FGF9, cyclin D1 CDK4 and CDK6. Therefore, miR-187 may present a new NSCLC treatment target by regulates cyclins-related protein expression.
机译:非小细胞肺癌(NSCLC)是肺癌的主要病理型,其总体5年生存率低。据报道,MIR-187在各种肿瘤类型中起主要角色。在这项研究中,我们探讨了MIR-187对NSCLC的影响。 QRT-PCR结果表明,NSCRC和癌细胞比正常组织和正常肺细胞较低。 miR-187表达水平与肿瘤大小,tnm阶段和总存活率相关。 MTS和菌落形成测定结果表明,高miR-187表达抑制NSCLC细胞增殖和菌落形成能力,流式细胞术显示MIR-187过表达在G0 / G1相位诱导细胞周期停滞。荧光素酶报告器测定结果显示FGF9是miR-187的靶标。 miR-187过表达降低了FGF9,Cyclin D1 CDK4和CDK6的表达。因此,MIR-187可以通过调节相关的细胞周期蛋白相关蛋白表达来提出新的NSCLC治疗靶标。

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