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 cavalently 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.
原文 | 英語 |
---|---|
頁(從 - 到) | 466-468 |
頁數 | 3 |
期刊 | Science |
卷 | 226 |
發行號 | 4673 |
出版狀態 | 已發佈 - 1984 |
對外發佈 | 是 |
ASJC Scopus subject areas
- 多學科