DNA
磷酸二酯键
核酸
拓扑异构酶
DNA损伤
阿霉素
体外
生物化学
化学
分子生物学
生物
核糖核酸
遗传学
化疗
基因
作者
K M Tewey,Thomas C. Rowe,Liu Yang,Brian Halligan,Leroy F. Liu
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:1984-10-26
卷期号:226 (4673): 466-468
被引量:1468
标识
DOI:10.1126/science.6093249
摘要
Adriamycin (doxorubicin), a potent antitumor drug in clinical use, interacts with nucleic acids and cell membranes, but the molecular basis for its antitumor activity is unknown. Similar to a number of intercalative antitumor drugs and nonintercalative epipodophyllotoxins (VP-16 and VM-26), adriamycin has been shown to induce single- and double-strand breaks in DNA. These strand breaks are unusual because a covalently bound protein appears to be associated with each broken phosphodiester bond. In studies in vitro, mammalian DNA topoisomerase II mediates DNA damage by adriamycin and other related antitumor drugs.
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