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首页> 外文期刊>OncoTargets and therapy >Targeting ZEB2 By microRNA-129 In Non-Small Cell Lung Cancer Suppresses Cell Proliferation, Invasion And Migration Via Regulating Wnt/β-Catenin Signaling Pathway And Epithelial–Mesenchymal Transition
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Targeting ZEB2 By microRNA-129 In Non-Small Cell Lung Cancer Suppresses Cell Proliferation, Invasion And Migration Via Regulating Wnt/β-Catenin Signaling Pathway And Epithelial–Mesenchymal Transition

机译:在非小细胞肺癌中通过MicroRNA-129靶向Zeb2,通过调节Wnt /β-catenin信号传导途径和上皮 - 间充质转换来抑制细胞增殖,侵袭和迁移

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Introduction: Non-small cell lung cancer (NSCLC) is a common cause of deaths all over the world. Emerging evidence has indicated that microRNA (miR) play key roles in NSCLC progression. We aimed to determine the functions of miR-129 in NSCLC. miR-129 was dramatically downregulated in NSCLC tissue samples and cells. The decreased miR-129 was found to be associated with poorer prognosis and malefic phenotype of NSCLC patients. We demonstrated that miR-129 upregulation could inhibit NSCLC cell growth. Furthermore, we also sought the molecular mechanism by which miR-129 repressed NSCLC development. Methods: QRT-PCR was applied to detect the expressions of miR-129 in 51 pairs of NSCLC tissue samples. We further performed the Kaplan–Meier analysis to determine the association between miR-129 expressions and the survival rate of NSCLC patients. We then measured the expression levels of miR-129 in NSCLC cell lines. After that, MTT assays were performed to determine the influence of miR-129 on A549 cell proliferation. Transwell assay was then conducted to explore the biological functions of miR-129 in invasion and migration of NSCLC cells. Results: Results showed that ZEB2 was directly targeted by miR-129 in NSCLC cell lines. Moreover, miR-129 restoration could inhibit EMT and Wnt/β-catenin in NSCLC cell lines. Conclusion: In short, all these results indicated that miR-129/ZEB2 axis maybe a useful diagnostic and prognostic biomarker for NSCLC treatment.
机译:简介:非小细胞肺癌(NSCLC)是世界各地死亡的常见原因。新兴的证据表明MicroRNA(MIR)在NSCLC进展中发挥关键作用。我们旨在确定MIR-129在NSCLC中的功能。 MIR-129在NSCLC组织样品和细胞中显着下调。发现下降的miR-129与NSCLC患者的预后和麦叶表型相关联。我们证明MiR-129上调可以抑制NSCLC细胞生长。此外,我们还寻求MiR-129压抑NSCLC发育的分子机制。方法:施用QRT-PCR以检测51对NMSCLC组织样品中miR-129的表达。我们进一步执行了Kaplan-Meier分析以确定MiR-129表达与NSCLC患者的生存率之间的关联。然后,我们测量了NSCLC细胞系中miR-129的表达水平。此后,进行MTT测定以确定miR-129对A549细胞增殖的影响。然后进行Transwell测定以探讨miR-129在侵袭和迁移Nsclc细胞的生物学功能。结果:结果表明,ZEB2在NSCLC细胞系中的miR-129直接靶向。此外,miR-129恢复可以抑制NSCLC细胞系中的EMT和WNT /β-连环蛋白。结论:简而言之,所有这些结果表明miR-129 / zeb2轴可能是用于NSCLC治疗的有用的诊断和预后生物标志物。

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