Clinical applications of quinone-containing alkylating agents

被引:57
作者
Begleiter, A
机构
[1] Manitoba Inst Cell Biol, Canc Care Manitoba, Winnipeg, MB R3E 0V9, Canada
[2] Univ Manitoba, Dept Internal Med, Winnipeg, MB, Canada
[3] Univ Manitoba, Dept Pharmacol & Therapeut, Winnipeg, MB, Canada
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2000年 / 5卷
关键词
quinone agents; alkylating agents; clinic; review;
D O I
10.2741/begleit
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
Quinone-containing alkylating agents are a class of chemical agents that have received considerable interest as anticancer drugs. These agents contain a quinone moiety that can be reduced and an alkylating group that can form covalent bonds with a variety of cellular components. The oxidation state of the quinone element can modulate the activity of the alkylating element, and reduction of the quinone is required for activation of the alkylating activity of many of these agents. The quinone element may also contribute to the cytotoxic activity of quinone-containing alkylating agents through the formation of reactive oxygen species during redox cycling. The natural product, mitomycin C, has been the most widely used quinone-containing alkylating agent in the clinic, but other quinone-containing alkylating agents like porfiromycin, diaziquone, carbazilquinone, triaziquone and EO9 havealso been used in the clinic for the treatment of cancer. In addition, many other quinone-containing alkylating agents have been tested in preclinical studies and the development of new agents is being actively pursued. This chapter describes the current and past clinical uses of these agents in the treatment of cancer and discusses new agents that are currently in clinical trials.
引用
收藏
页码:E153 / E171
页数:19
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