IARS2 silencing induces non-small cell lung cancer cells proliferation inhibition, cell cycle arrest and promotes cell apoptosis

被引:10
|
作者
Yin, J. [1 ]
Liu, W. [2 ]
Li, R. [3 ]
Liu, J. [1 ]
Zhang, Y. [1 ]
Tang, W. [1 ]
Wang, K. [1 ]
机构
[1] Jilin Univ, Affiliated Hosp 2, Dept Resp Med, Changchun 130041, Jilin, Peoples R China
[2] Jilin Univ, Bethune Hosp 1, Dept Thorac Surg, Changchun 130021, Jilin, Peoples R China
[3] Jilin Univ, Affiliated Hosp 2, Dept Urinary Surg, Changchun 130041, Jilin, Peoples R China
关键词
IARS2; silencing; NSCLC; cell proliferation; cell apoptosis; cell cycle; TRANSFER-RNA SYNTHETASE; MITOCHONDRIA-DEPENDENT APOPTOSIS; HUMAN COLON-CANCER; SHORT-TERM; EXPRESSION; GROWTH; BAX; THERAPY; DISEASE; TARGET;
D O I
10.4149/neo_2016_008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The purpose of this study was to investigate the potential role of Ileucyl-tRNA synthetase (IARS2) silencing in non-small cell lung cancer (NSCLC). The silencing of IARS2 in H1299 cells and A549 cells were performed by lentivirus encoding shRNAs. The efficiency of IARS2 silencing was detected by quantitative real time PCR and western blot. The effects of IARS2 silencing on cell growth, cell apoptosis, cell cycle and cell colony formation ability were assessed by cells counting, MTT assay, flow cytometer analysis and soft agar colony formation assay, respectively. Compared with negative control group, IARS2 was significantly knockdown by transfection with lentivirus encoding shRNA of IARS2. The IARS2 silencing significantly inhibited the cells proliferation and cells colony formation ability, induced cell cycle arrest at G1/S phase and promoted cell apoptosis. IARS2 silencing induced NSCLC cells growth inhibition, cell cycle arrest and promoted cell apoptosis. These results suggest that IARS2 may be a novel target for the treatment of NSCLC.
引用
收藏
页码:64 / 71
页数:8
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