Abstract
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.
Original language | English |
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Pages (from-to) | 23-26 |
Number of pages | 4 |
Journal | Cancer Cells |
Volume | 2 |
Issue number | 1 |
Publication status | Published - 1990 |
Externally published | Yes |
ASJC Scopus subject areas
- Cancer Research