中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
salvicineanoveltopoisomeraseiiinhibitorexertsitspotentanticanceractivitybyrosgeneration1

文献类型:期刊论文

作者Linghua MENG; Jian DING
刊名actapharmacologicasinica
出版日期2007
卷号28期号:9页码:1460
关键词salvicine topoisomerase II ROS DNA damage multidrug-resisitant antimetastasis
ISSN号1671-4083
英文摘要Salvicine is a novel diterpenoid quinone compound obtained by structural modification of a natural product lead isolated from a Chinese herb with potent growth inhibitory activity against a wide spectrum of human tumor cells in vitro and in mice bearing human tumor xenografts. Salvicine has also been found to have a profound cytotoxic effect on multidrug-resisitant (MDR) cells. Moreover, Salvicine significantly reduced the lung metastatic foci of MDA-MB-435 orthotopic xenograft. Recent studies demonstrated that salvicine is a novel non-intercalative topoisomerase II (Topo II) poison by binding to the ATPase domain, promoting DNA-Topo II binding and inhibiting Topo II-mediated DNA relegation and ATP hydrolysis. Further studies have indicated that salcivine-elicited ROS plays a central role in salvicine-induced cellular response including Topo II inhibition, DNA damage, circumventing MDR and tumor cell adhesion inhibition.
语种英语
源URL[http://119.78.100.183/handle/2S10ELR8/287491]  
专题中国科学院上海药物研究所
作者单位中国科学院上海药物研究所
推荐引用方式
GB/T 7714
Linghua MENG,Jian DING. salvicineanoveltopoisomeraseiiinhibitorexertsitspotentanticanceractivitybyrosgeneration1[J]. actapharmacologicasinica,2007,28(9):1460.
APA Linghua MENG,&Jian DING.(2007).salvicineanoveltopoisomeraseiiinhibitorexertsitspotentanticanceractivitybyrosgeneration1.actapharmacologicasinica,28(9),1460.
MLA Linghua MENG,et al."salvicineanoveltopoisomeraseiiinhibitorexertsitspotentanticanceractivitybyrosgeneration1".actapharmacologicasinica 28.9(2007):1460.

入库方式: OAI收割

来源:上海药物研究所

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