Ecteinascidin 743: a novel anticancer drug with a unique mechanism of action

被引:121
作者
Aune, GJ [1 ]
Furuta, T [1 ]
Pommier, Y [1 ]
机构
[1] NCI, Ctr Canc Res, Mol Pharmacol Lab, Bethesda, MD 20892 USA
关键词
cancer chemotherapy; DNA alkylation; DNA binding; DNA repair; minor groove binder; transcription;
D O I
10.1097/00001813-200207000-00001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ecteinascidin 743 (Et743) is an interesting compound in phase II/III clinical trials. Its chemistry is complex, its mechanism of action is original and it is active in human cancers, such as sarcomas refractory to conventional chemotherapy. The present review describes the discovery of the drug, its specific interactions with DNA and its reversible alkylation mechanism with guanine N-2 in the DNA minor groove. Et743 is a selective transcription inhibitor, which has the unique characteristic of poisoning transcription-coupled nucleotide excision repair. Understanding the molecular pharmacology of Et743 should help in deciding which patients should receive Et743 treatments and which agents should be most useful in association. [(C) 2002 Lippincott Williams Wilkins].
引用
收藏
页码:545 / 555
页数:11
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