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miR-133b Inhibits Cell Growth, Migration, and Invasion by Targeting MMP9 in Non-Small Cell Lung Cancer
被引:32
|作者:
Zhen, Yan
[1
]
Liu, Jia
[1
,2
]
Huang, Yujie
[1
,2
]
Wang, Yajun
[1
]
Li, Wen
[1
,2
]
Wu, Jun
[1
,2
]
机构:
[1] Guangdong Med Univ, Affiliated Hosp, Inst Resp Dis, Zhanjiang, Peoples R China
[2] Guangdong Med Univ, Affiliated Hosp, Dept Resp Med, Ren Min Rd South 57, Zhanjiang 524001, Peoples R China
关键词:
miR-133b;
Matrix metallopeptidase 9 (MMP9);
Non-small cell lung cancer (NSCLC);
Cell growth;
Migration and invasion;
METASTASIS;
SURVIVAL;
D O I:
10.3727/096504016X14800889609439
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
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.
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页码:1109 / 1116
页数:8
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