Inhibition of miR-92b suppresses nonsmall cell lung cancer cells growth and motility by targeting RECK

被引:58
作者
Lei, Lin [1 ]
Huang, Yaping [2 ]
Gong, Wenrong [3 ]
机构
[1] Xiangyang Cent Hosp, Dept Oncol, Xiangyang 441021, Peoples R China
[2] Xiangyang Cent Hosp, Dept Resp Med, Xiangyang 441021, Peoples R China
[3] Hubei Univ Arts & Sci, Inst Oncol, Coll Med, Xiangyang 441053, Peoples R China
关键词
miR-92; Nonsmall cell lung cancer; Growth; Migration; Invasion; CLINICAL-SIGNIFICANCE; TUMOR-SUPPRESSOR; DOWN-REGULATION; GASTRIC-CANCER; PROLIFERATION; EXPRESSION; MICRORNA; INVASION; METHYLATION; CARCINOMA;
D O I
10.1007/s11010-013-1882-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
microRNAs play critical roles in the progression and metastasis of nonsmall cell lung cancer (NSCLC). miR-92b acts as an oncogene in some malignancies; however, its role in NSCLC remains poorly understood. Here, we found that miR-92b was significantly increased in human NSCLC tissues and cell lines. Inhibition of miR-92b remarkably suppressed cell proliferation, migration, and invasion of NSCLC cells. Reversion-inducing-cysteine-rich protein with kazal motifs (RECK) was identified to be a target of miR-92b. Expression of miR-92b was negatively correlated with RECK in NSCLC tissues. Collectively, miR-92b might promote NSCLC cell growth and motility partially by inhibiting RECK.
引用
收藏
页码:171 / 176
页数:6
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