Zhen Yan, Liu Jia, Huang Yujie, Wang Yajun, Li Wen, Wu Jun
Oncol Res. 2017 Aug 7;25(7):1109-1116. doi: 10.3727/096504016X14800889609439. Epub 2016 Nov 29.
Although increasing evidence indicates that the deregulation of microRNAs (miRNAs) contributes to tumorigenesis and invasion, little is known about the role of miR-133b in human non-small cell lung cancer (NSCLC). In the present study, we revealed that the introduction of miR-133b dramatically suppressed NSCLC cell growth, migration, and invasion in vitro. On the contrary, miR-133b inhibitors promoted cell growth, migration, and invasion in vitro. Further studies revealed that matrix metallopeptidase 9 (MMP9) is a direct target gene of miR-133b. Silencing MMP9 inhibited cell growth, migration, and invasion of NSCLC cells, which was consistent with the effect of miR-133b overexpression. In clinical specimens, reduced miR-133b was an unfavorable factor and negatively correlated with MMP9 expression. Our studies demonstrate that miR-133b inhibits cell growth, migration, and invasion by targeting MMP9 in NSCLC.
尽管越来越多的证据表明,微小RNA(miRNA)的失调与肿瘤发生和侵袭有关,但关于miR-133b在人类非小细胞肺癌(NSCLC)中的作用知之甚少。在本研究中,我们发现引入miR-133b可显著抑制NSCLC细胞在体外的生长、迁移和侵袭。相反,miR-133b抑制剂可促进细胞在体外的生长、迁移和侵袭。进一步研究表明,基质金属蛋白酶9(MMP9)是miR-133b的直接靶基因。沉默MMP9可抑制NSCLC细胞的生长、迁移和侵袭,这与miR-133b过表达的效果一致。在临床标本中,miR-133b表达降低是一个不利因素,且与MMP9表达呈负相关。我们的研究表明,miR-133b在NSCLC中通过靶向MMP9抑制细胞生长、迁移和侵袭。