摘要
Our model proposes that topoisomerase-targeting antitumor drugs form reversible drug-enzyme-DNA complexes that collide with the DNA and RNA synthesis machineries. On collisions, the complexes lose their reversibility, and generate lethal double-strand DNA breaks. Further investigations of topoisomerase action will allow this model to be refined, and may ultimately lead to the development of more effective anticancer drugs.
原文 | 英語 |
---|---|
頁(從 - 到) | 23-26 |
頁數 | 4 |
期刊 | Cancer Cells |
卷 | 2 |
發行號 | 1 |
出版狀態 | 已發佈 - 1990 |
對外發佈 | 是 |
ASJC Scopus subject areas
- 癌症研究