Wassermann K, Markovits J, Jaxel C, Capranico G, Kohn K W, Pommier Y
Division of Cancer Treatment, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892.
Mol Pharmacol. 1990 Jul;38(1):38-45.
The effect of cyanomorpholinyldoxorubicin, morpholinyldoxorubicin, doxorubicin, and Actinomycin D were studied on purified mouse leukemia (L1210) DNA topoisomerases I and II. DNA unwinding and cross-linking were also studied. It was found that 1) morpholinyldoxorubicin, cyanomorpholinyldoxorubicin, and Actinomycin D (but not doxorubicin) stimulated DNA topoisomerase I-induced cleavage at specific DNA sites; 2) only doxorubicin and Actinomycin D stimulated DNA cleavage by DNA topoisomerase II; 3) at higher drug concentrations, DNA intercalators suppressed enzyme-mediated DNA cleavage induced by DNA topoisomerase I, as well as topoisomerase II; 4) only cyanomorpholinyldoxorubicin produced DNA-DNA cross-links; no DNA unwinding could be observed; and 5) DNA intercalation (unwinding) potency of morpholinyldoxorubicin was about 2-fold less than that of doxorubicin. The data indicate that some DNA intercalators are not only inhibitors of DNA topoisomerase II but act also on DNA topoisomerase I. The stabilization of cleavage intermediates by intercalators may have a common mechanism for DNA topoisomerase I and DNA topoisomerase II.
研究了氰基吗啉基阿霉素、吗啉基阿霉素、阿霉素和放线菌素D对纯化的小鼠白血病(L1210)DNA拓扑异构酶I和II的作用。还研究了DNA解旋和交联情况。结果发现:1)吗啉基阿霉素、氰基吗啉基阿霉素和放线菌素D(而非阿霉素)能刺激DNA拓扑异构酶I在特定DNA位点诱导的切割;2)只有阿霉素和放线菌素D能刺激DNA拓扑异构酶II介导的DNA切割;3)在较高药物浓度下,DNA嵌入剂会抑制DNA拓扑异构酶I以及拓扑异构酶II介导的酶促DNA切割;4)只有氰基吗啉基阿霉素能产生DNA-DNA交联;未观察到DNA解旋;5)吗啉基阿霉素的DNA嵌入(解旋)能力比阿霉素低约2倍。数据表明,一些DNA嵌入剂不仅是DNA拓扑异构酶II的抑制剂,对DNA拓扑异构酶I也有作用。嵌入剂对切割中间体的稳定作用可能对DNA拓扑异构酶I和DNA拓扑异构酶II具有共同机制。