Curcumin promotes apoptosis in A549/DDP multidrug-resistant human lung adenocarcinoma cells through an miRNA signaling pathway

被引:138
作者
Zhang, Jian [3 ]
Zhang, Tao [2 ]
Ti, Xinyu [3 ]
Shi, Jieran [3 ]
Wu, Changgui [3 ]
Ren, Xinling [3 ]
Yin, Hong [1 ]
机构
[1] Fourth Mil Med Univ, Xijing Hosp, Med Image Ctr, Xian 710032, Peoples R China
[2] Fourth Mil Med Univ, Tangdu Hosp, Dept Thorac Surg, Xian 710038, Peoples R China
[3] Fourth Mil Med Univ, Xijing Hosp, Dept Resp Med, Xian 710032, Peoples R China
基金
中国国家自然科学基金;
关键词
Curcumin; Multidrug-resistant human lung adenocarcinoma cell line A549/DDP; Apoptosis; miR-186; INHIBITS PROLIFERATION; CANCER; EXPRESSION; GROWTH; GENE; MICRORNAS; PCR;
D O I
10.1016/j.bbrc.2010.07.013
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
Curcumin extracted from the rhizomes of Curcuma longa L has been shown to have inhibitory effects on cancers through its anti-proliferative and pro-apoptotic activities. Emerging evidence demonstrates that curcumin can overcome drug resistance to classical chemotherapies. Thus, the mechanisms underlying the anti-tumor activities of curcumin require further study. In our study, we first demonstrated that curcumin had anti-cancer effects on A549/DDP multidrug-resistant human lung adenocarcinoma cells. Further studies showed that curcumin altered miRNA expression; in particular, significantly downregulated the expression of miR-186* in A549/DDP. In addition, transfection of cells with a miR-186* inhibitor promoted A549/DDP apoptosis, and overexpression of miR-186* significantly inhibited curcumin-induced apoptosis in A549/DDP cells. These observations suggest that miR-186* may serve as a potential gene therapy target for refractory lung cancer that is sensitive to curcumin. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 6
页数:6
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