首页> 美国卫生研究院文献>International Journal of Clinical and Experimental Pathology >MicroRNA-139-5p inhibits cell proliferation and invasion by targeting insulin-like growth factor 1 receptor in human non-small cell lung cancer
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MicroRNA-139-5p inhibits cell proliferation and invasion by targeting insulin-like growth factor 1 receptor in human non-small cell lung cancer

机译:MicroRNA-139-5p通过靶向人非小细胞肺癌中的胰岛素样生长因子1受体抑制细胞增殖和侵袭

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摘要

Introduction: Increasing evidence suggested that microRNAs (miRNAs) play a critical role in tumorigenesis. Decreased expression of miRNA-139-5p has been observed in various types of cancers. However, the biological function of miRNA-139-5p in non-small cell lung cancer (NSCLC) is still largely unknown. Methods: Quantitative real-time PCR (qRT-PCR) was used to explore the expression level of miRNA-139-5p in NSCLC tissues and cell lines. Then, we investigated the role of miRNA-139-5p to determine its potential roles on lung cancer cell proliferation, migration and invasion in vitro. A luciferase reporter assay was performed to confirm the target gene of miRNA-139-5p and the results were validated in renal cancer cells. Results: miRNA-139-5p was significantly decreased in NSCLC tissues and cell lines. Over-expression of miRNA-139-5p could inhibit lung cancer cell proliferation, migration, and invasion in vitro. Furthermore, we identified insulin-like growth factor 1 receptor (IGF1R) as a target of miR-139-5p and miR-139-5p function as a tumor suppressor via targeting IGF1R in NSCLC. Conclusions: Our results indicated that miR-139-5p acts as a tumor suppressor in NSCLC partially via down-regulating IGF1R expression.
机译:简介:越来越多的证据表明,microRNA(miRNA)在肿瘤发生中起关键作用。在各种类型的癌症中均观察到miRNA-139-5p的表达降低。但是,miRNA-139-5p在非小细胞肺癌(NSCLC)中的生物学功能仍是未知之数。方法:采用实时荧光定量PCR(qRT-PCR)检测miRNA-139-5p在NSCLC组织和细胞株中的表达水平。然后,我们调查了miRNA-139-5p的作用,以确定其在体外对肺癌细胞增殖,迁移和侵袭的潜在作用。进行荧光素酶报告基因测定以确认miRNA-139-5p的靶基因,并在肾癌细胞中验证了结果。结果:NSCLC组织和细胞系中的miRNA-139-5p明显降低。 miRNA-139-5p的过表达可在体外抑制肺癌细胞的增殖,迁移和侵袭。此外,我们通过靶向NSCLC中的IGF1R,确定了胰岛素样生长因子1受体(IGF1R)作为miR-139-5p的靶标,而miR-139-5p作为肿瘤抑制因子。结论:我们的结果表明,miR-139-5p部分通过下调IGF1R表达而在NSCLC中起抑癌作用。

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