Sinha B K, Mimnaugh E G
Medicine Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Free Radic Biol Med. 1990;8(6):567-81. doi: 10.1016/0891-5849(90)90155-c.
Certain anticancer agents form free radical intermediates during enzymatic activation. Recent studies have indicated that free radicals generated from adriamycin and mitomycin C may play a critical role in their toxicity to human tumor cells. Furthermore, it is becoming increasingly apparent that reduced drug activation and or enhanced detoxification of reactive oxygen species may be related to the resistance to these anticancer agents by certain tumor cell lines. The purposes of this review are to summarize the evidence pointing toward the significance of free radicals formation in drug toxicity and to evaluate the role of decreased free radical formation and enhanced free radical scavenging and detoxification in the development of anticancer drug resistance by a spectrum of tumor cell types. Studies failing to support the participation of oxyradicals in the cytotoxicity and resistance of adriamycin are also discussed.
某些抗癌药物在酶促活化过程中会形成自由基中间体。最近的研究表明,阿霉素和丝裂霉素C产生的自由基可能在其对人肿瘤细胞的毒性中起关键作用。此外,越来越明显的是,药物活化减少和/或活性氧解毒增强可能与某些肿瘤细胞系对这些抗癌药物的耐药性有关。本综述的目的是总结指向自由基形成在药物毒性中的重要性的证据,并评估自由基形成减少、自由基清除和解毒增强在一系列肿瘤细胞类型的抗癌药物耐药性发展中的作用。还讨论了不支持氧自由基参与阿霉素细胞毒性和耐药性的研究。