MiRNA-107 enhances chemosensitivity to paclitaxel by targeting antiapoptotic factor Bcl-w in non small cell lung cancer

被引:2
作者
Lu, Chaojing [1 ]
Xie, Zhibing [2 ]
Peng, Qingzhen [2 ]
机构
[1] Changhai Hosp, Dept Thorac Surg, Shanghai, Peoples R China
[2] Wuhan Univ Sci & Technol, Dept Resp Med, Xiaogan Cent Hosp, Xiaogan, Peoples R China
来源
AMERICAN JOURNAL OF CANCER RESEARCH | 2017年 / 7卷 / 09期
关键词
Non small cell lung cancer; chemoresistance; microRNA-107; Bcl-w; PI3K-Akt pathway; INHIBITS TUMOR-GROWTH; GASTRIC-CANCER; BREAST-CANCER; RESISTANCE; CHEMOTHERAPY; APOPTOSIS; PROLIFERATION; MITOCHONDRIAL; POLYMORPHISM; SENSITIVITY;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of this study is to elucidate whether and how miR-107 participates in the modulation of paclitaxel sensitivity in non small cell lung cancer (NSCLC). By qRT-PCR, we found that miR-107 is significantly down-regulated in paclitaxel-resistant A549/Taxol cells compared with corresponding paclitaxel-sensitive counterparts. Overexpression of miR-107 suppresses paclitaxel resistance of A549/Taxol cells through directly inhibiting Bcl-w. Overexpression of miR-107 promotes apoptosis and inhibits proliferation and mobility of A549/Taxol cells under treatment with paclitaxel in vitro. Moreover, miR-107 inhibits in vivo paclitaxel resistance in xenograft model. MiR-107/Bcl-w axis regulates paclitaxel chemoresistance through PI3K-Akt pathway. Our results suggest that up-regulation of miR-107 resensitizes paclitaxel-resistant NSCLC cells by targeting Bcl-w, which reveals a potential mechanism of miR-107 in reversing drug resistance.
引用
收藏
页码:1863 / 1873
页数:11
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