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首页> 外文期刊>Thoracic cancer. >microRNA ‐100 functions as a tumor suppressor in non‐small cell lung cancer via regulating epithelial‐mesenchymal transition and Wnt/β‐catenin by targeting HOXA1
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microRNA ‐100 functions as a tumor suppressor in non‐small cell lung cancer via regulating epithelial‐mesenchymal transition and Wnt/β‐catenin by targeting HOXA1

机译:通过靶向Hoxa1,MicroRNA -100通过调节上皮 - 间充质转换和Wnt /β-catenin来用作非小细胞肺癌中的肿瘤抑制剂

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BACKGROUND:Non-small cell lung cancer (NSCLC) is a leading subtype in lung cancer, with high morbidities and mortalities worldwide. microRNA (miRNA) has appeared to play indispensable roles in a variety of solid carcinomas. The current study focused on the functions of miR-100 in NSCLC.METHODS:qRT-PCR was performed to detect miR-100 and HOXA1 expressions in NSCLC tissues and cells. MTT and transwell assays were used to determine the functions of miR-100 in NSCLC cell proliferation, invasion and migration abilities. Western blot was used to measure related protein expressions.RESULTS:qRT-PCR results showed that miR-100 expressions were dramatically decreased in NSCLC tissues. MTT assays indicated that miR-100 restoration inhibited NSCLC cell proliferation. Furthermore, transwell assay was performed to determine the impacts of miR-100 on NSCLC invasion and migration abilities. As expected, the invasion and migration capacities were significantly repressed. Direct interactions between HOXA1 and miR-100 were also verified via dual-luciferase reporter assays. Western blot analysis demonstrated that miR-100 exerted suppressive functions via regulating EMT and Wnt/β-catenin in NSCLC cells.CONCLUSIONS:Our results showed that miR-100 served antitumor roles in NSCLC, providing new evidence of miR-100 as a promising therapeutic biomarker in NSCLC.? 2020 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd.
机译:背景:非小细胞肺癌(NSCLC)是肺癌的主要亚型,在全球性病和全世界都有高病态和死亡率。 MicroRNA(miRNA)似乎在各种固体癌中发挥不可或缺的作用。目前的研究专注于NSCLC中MIR-100的功能。方法:进行QRT-PCR以检测NSCLC组织和细胞中的miR-100和Hoxa1表达。 MTT和Transwell测定用于确定MIR-100在NSCLC细胞增殖,入侵和迁移能力中的功能。 Western印迹用于测量相关的蛋白质表达。结果:QRT-PCR结果表明,NSCLC组织中miR-100表达显着降低。 MTT测定表明miR-100恢复抑制了NSCLC细胞增殖。此外,进行Transwell测定以确定miR-100对NSCLC入侵和移民能力的影响。正如预期的那样,入侵和移民能力大大压抑。还通过双荧光素酶报告分析验证了Hoxa1和miR-100之间的直接相互作用。 Western印迹分析证明MiR-100通过在NMSCLC细胞中调节EMT和Wnt /β-catenin施加抑制功能。结论:我们的结果表明,MIR-100在NSCLC中提供了抗肿瘤作用,提供了MIR-100作为有前途治疗的新证据NSCLC中的生物标志物。 2020作者。中国肺部肿瘤集团和约翰瓦里和儿子澳大利亚发表的胸癌

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