The role of miR-139-5p and miR-206 in non-small cell lung cancer (NSCLC) by targeting c-Met

Chengcao Sun, Shu-Jun Li, Dejia Li
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Abstract

Increasing evidences have confirmed that ectopic miRNAs are key regulatory factors in various types of cancers. Both hsa-miRNA-206 (miR-206) and hsa-miRNA-139-5p (miR-139-5p) have been demonstrated that possess anticancer properties in a variety of tissues and organs. In our recent investigations, we discovered miR-139-5p and miR-206 played a crucial role in lung cancer progression. There were extremely low levels of miR-206 and miR-139-5p in NSCLC (non-small cell lung cancer) cell lines as well as expression of them were inhibited in lung cancer tissues, respectively. Moreover, we found that miR-206 through targeting 3′-UTR(3'-untranslated region )of Bcl-2 and c-Met mRNA that promoted cell apoptosis as well as suppressed non-small cell lung cancer SK-MES-1 and A549 cells colony formation, growth, invasion and metastasis. The analogical phenomenon was also discovered in miR-139-5p that targeted tumorigenic c-Met, which contributed to promotion of apoptosis and inhibition of cell proliferation and migration in non-small cell lung cancer.
miR-139-5p和miR-206靶向c-Met在非小细胞肺癌(NSCLC)中的作用
越来越多的证据证实,异位mirna是各种类型癌症的关键调控因子。hsa-miRNA-206 (miR-206)和hsa-miRNA-139-5p (miR-139-5p)已被证明在多种组织和器官中具有抗癌特性。在我们最近的研究中,我们发现miR-139-5p和miR-206在肺癌进展中起着至关重要的作用。miR-206和miR-139-5p在NSCLC(非小细胞肺癌)细胞系中表达水平极低,在肺癌组织中表达受到抑制。此外,我们发现miR-206通过靶向Bcl-2和c-Met mRNA的3' -UTR(3'-未翻译区)促进细胞凋亡,抑制非小细胞肺癌SK-MES-1和A549细胞的集落形成、生长、侵袭和转移。在靶向致瘤性c-Met的miR-139-5p中也发现了类似的现象,这有助于促进非小细胞肺癌细胞凋亡,抑制细胞增殖和迁移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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