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MiR-153 inhibits migration and invasion of human non-small-cell lung cancer by targeting ADAM19

机译:MiR-153通过靶向Adam19抑制人类非小细胞肺癌的迁移和侵袭

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MiR-153 was reported to be dysregulated in some human cancers. However, the function and mechanism of miR-153 in lung cancer cells remains unknown. In this study, we investigated the role of miR-153 in human non-small-cell lung cancer (NSCLC). Using qRT-PCR, we demonstrated that miR-153 was significantly decreased in clinical NSCLC tissues and cell lines, and downregulation of miR-153 was significantly correlated with lymph node status. We further found that ectopic expression of miR-153 significantly inhibited the proliferation and migration and invasion of NSCLC cells in vitro, suggesting that miR-153 may be a novel tumor suppressor in NSCLC. Further integrated analysis revealed that ADAM19 is as a direct and functional target of miR-153. Luciferase reporter assay demonstrated that miR-153 directly targeted 3'UTR of ADAM19, and correlation analysis revealed an inverse correlation between miR-153 and ADAM19 mRNA levels in clinical NSCLC tissues. Knockdown of ADAM19 inhibited migration and invasion of NSCLC cells which was similar with effects of overexpression of miR-153, while overexpression of ADAM19 attenuated the function of miR-153 in NSCLC cells. Taken together, our results highlight the significance of miR-153 and ADAM19 in the development and progression of NSCLC. (C) 2014 Elsevier Inc. All rights reserved.
机译:据报道,MiR-153在某些人类癌症中令人讨发。然而,miR-153在肺癌细胞中的功能和机制仍然未知。在这项研究中,我们研究了miR-153在人非小细胞肺癌(NSCLC)中的作用。使用QRT-PCR,我们证明了MIR-153在临床NMSCLC组织和细胞系中显着降低,MIR-153的下调与淋巴结状态明显相关。我们进一步发现miR-153的异位表达显着抑制了体外细胞的增殖和迁移和侵袭,表明miR-153可以是NSCLC中的新型肿瘤抑制剂。进一步的综合分析表明,ADAM19是MIR-153的直接和功能靶标。荧光素酶报告器测定证明了MIR-153直接靶向ADAM19的3'UTR,并且相关性分析显示了临床NSCLC组织中miR-153和ADAM19 mRNA水平之间的反比相关性。 ADAM19的敲低抑制了与miR-153的过表达的效果类似的NSCLC细胞的迁移和侵袭,而ADAM19的过度表达衰减了NSCLC细胞中miR-153的功能。在一起,我们的结果突出了MIR-153和ADAM19在NSCLC开发和进展中的意义。 (c)2014年elsevier Inc.保留所有权利。

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