salvicineanoveltopoisomeraseiiinhibitorexertsitspotentanticanceractivitybyrosgeneration1
文献类型:期刊论文
作者 | Linghua MENG![]() ![]() |
刊名 | actapharmacologicasinica
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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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