Methyl protodioscin induces G2/M cell cycle arrest and apoptosis. in HepG2 liver cancer cells

被引:83
|
作者
Wang, Guanghui
Chen, Haifeng
Huang, Minghui
Wang, Naili
Zhang, Jinchao
Zhang, Yaou
Bai, Ganrong
Fong, Wang-Fun
Yang, Mengsu
Yao, Xinsheng
机构
[1] City Univ Hong Kong, Dept Biochem & Chem, Kowloon, Hong Kong, Peoples R China
[2] City Univ Hong Kong, Shenzhen Biotech & Hlth Ctr, Shenzhen Inst, Kowloon 518057, Hong Kong, Peoples R China
[3] Shenyang Pharmaceut Univ, Dept Nat Prod Chem, Shenyang 110016, Peoples R China
[4] Tsing Hua Univ, Grad Sch, Shenzhen 518055, Peoples R China
[5] Univ Town, Shenzhen Res Ctr Tradit Chinese Med & Nat Prod, Shenzhen 518055, Peoples R China
关键词
methyl protodioscin; G(2)/M arrest; apoptosis;
D O I
10.1016/j.canlet.2005.10.050
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Methyl protodioscin (NSC-698790) is one of the main bioactive components in the traditional Chinese medicine Dioscorea collettii var. hypoglauca (Dioscoreaceae). In this study, we investigated the anti-proliferative effect of methyl protodioscin on the HepG2 cells and the mechanism of the induced cytotoxicity. Treatment of methyl protodioscin resulted in G2/M arrest and apoptosis in HepG2 cells. These effects were attributed to down-regulation of Cyclin 131 and the signaling pathways leading to up-regulation of Bax and down-regulation of BCL2, suggesting that methyl protodioscin may be a novel anti-mitotic agent. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:102 / 109
页数:8
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