Piperlongumine is a novel nuclear export inhibitor with potent anticancer activity

被引:38
作者
Niu, Mingshan [1 ,2 ,4 ]
Xu, Xiaoyu [1 ,2 ]
Shen, Yangling [1 ,2 ]
Yao, Yao [1 ,2 ,4 ]
Qiao, Jianlin [1 ,2 ,4 ]
Zhu, Feng [1 ,2 ]
Zeng, Lingyu [1 ,2 ,4 ]
Liu, Xuejiao [3 ]
Xu, Kailin [1 ,2 ,4 ]
机构
[1] Xuzhou Med Coll, Blood Dis Inst, Xuzhou, Jiangsu, Peoples R China
[2] Xuzhou Med Coll, Jiangsu Key Lab Bone Marrow Stem Cell, Xuzhou, Jiangsu, Peoples R China
[3] Xuzhou Med Coll, Inst Nervous Syst Dis, Xuzhou, Jiangsu, Peoples R China
[4] Xuzhou Med Coll, Affiliated Hosp, Dept Hematol, Xuzhou, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Piperlongumine; Nuclear protein export; CRM1; Anti-cancer; SELECTIVE INHIBITORS; APOPTOSIS; CELLS; PROLIFERATION; RELEASE; GROWTH; CRM1;
D O I
10.1016/j.cbi.2015.05.016
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
Piperlongumine is a natural compound recently identified to be toxic selectively to tumor cells in vitro and in vivo. However, the molecular mechanism underlying its anti-tumor action still remains unclear. In this report, we describe another novel mechanism by which piperlongumine mediates its anti-tumor effects. We found that piperlongumine is a novel nuclear export inhibitor. Piperlongumine could induce nuclear retention of tumor suppressor proteins and inhibit the interactions between CRM1 and these proteins. Piperlongumine could directly bind to the conserved Cys528 of CRM1 but not to a Cys528 mutant peptide. More importantly, cancer cells expressing mutant CRM1 (C528S) are resistant to piperlongumine, demonstrating the nuclear export inhibition via direct interaction with Cys528 of CRM1. The inhibition of nuclear export by piperlongumine may account for its therapeutic properties in cancer diseases. Our findings provide a good starting point for development of novel CRM1 inhibitors. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:66 / 72
页数:7
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