Taxol is an antitumor drug which, as its mechanism of action, promotes
microtubule assembly in vitro. Camptothecin (CPT) is an anticancer ag
ent with the peculiar mechanism of poisoning eukaryotic DNA topoisomer
ase I. Both drugs are in clinical trials and their chemotherapeutic ef
ficacy seems promising in refractory human ovarian cancer. We studied
the molecular and cellular pharmacology of the two drugs when administ
ered simultaneously toward human ovarian cancer cell line A2780. Taxol
inhibits CPT-induced single-strand breaks as well as CPT-induced cyto
toxicity. Taken together, our experiments indicate that the two drugs
might interact with the same class of nuclear enzyme, i.e. DNA topoiso
merase I.