Suppression of EIF4G2 by miR-379 potentiates the cisplatin chemosensitivity in nonsmall cell lung cancer cells

被引:48
作者
Hao, Guang-jun [1 ]
Hao, Hai-jun [2 ]
Ding, Yan-hui [1 ]
Wen, Hui [1 ]
Li, Xiao-feng [1 ]
Wang, Qian-ru [1 ]
Zhang, Bing-bing [1 ]
机构
[1] First Hosp Yulin City, Dept Oncol, Yulin City, Peoples R China
[2] First Hosp Yulin City, Dept Clin Lab, 59 Wenhua Rd, Yulin City 718000, Shaanxi Provinc, Peoples R China
关键词
chemoresistance; cisplatin; EIF4F; lung cancer; miRNAs; ADENOCARCINOMA CELLS; CHEMORESISTANCE; RESISTANCE; SENSITIVITY; METASTASIS; TRANSITION; PROMOTES; INVASION; CLUSTER;
D O I
10.1002/1873-3468.12566
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although microRNAs and EIF4G2 are both known to play pivotal roles in cancer progression, it remains unknown whether these pathways regulate chemosensitivity in a coordinated manner. Here, we show that miR-379 expression is significantly downregulated in chemoresistant nonsmall cell lung cancer (NSCLC) tissues and cells. Manipulation of miR-379 levels could alter the in vitro and in vivo cisplatin (CDDP) resistance in lung cancer (LCa) cells. Mechanistically, miR-379 potentiated LCa chemosensitivity via modulation of CDDP-induced apoptosis by directly targeting the EIF4G2 3UTR. Additionally, we observed an inverse correlation between miR-379 and EIF4G2 expression in LCa tissues from patients with CDDP-based chemotherapy. Together, our findings shed new light on the potential involvement of miR-379/EIF4G2 cascade in the pathogenesis of CDDP resistance in LCa.
引用
收藏
页码:636 / 645
页数:10
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