Ridge G S, Bailly C, Graves D E, Waring M J
Department of Pharmacology, University of Cambridge, UK.
Nucleic Acids Res. 1994 Dec 11;22(24):5241-6. doi: 10.1093/nar/22.24.5241.
The antitumour antibiotic actinomycin D normally binds to DNA by intercalation at sequences containing the CpG step, but in the presence of daunomycin it has been reported to interact with poly(dA-dT). This observation has neither been confirmed nor explained. Here we have used a photoreactive 7-azido derivative of actinomycin to study the effect of daunomycin on its binding to three DNA fragments. Daunomycin did indeed alter the binding of actinomycin to the DNA, such that the antibiotic was displaced from its primary GpC sites onto secondary sites in the DNA, though not to AT regions especially. These findings suggest a possible scientific explanation for the increased toxicity seen during combination chemotherapy with these two drugs.
抗肿瘤抗生素放线菌素D通常通过插入含有CpG步移序列的DNA来与之结合,但据报道,在柔红霉素存在的情况下,它会与聚(dA-dT)相互作用。这一观察结果既未得到证实,也未得到解释。在这里,我们使用了一种光反应性的放线菌素7-叠氮衍生物来研究柔红霉素对其与三个DNA片段结合的影响。柔红霉素确实改变了放线菌素与DNA的结合,使得抗生素从其主要的GpC位点转移到DNA的二级位点,不过并非特别转移到AT区域。这些发现为这两种药物联合化疗期间观察到的毒性增加提供了一种可能的科学解释。