An evaluation of the effects of combination chemotherapy in vitro using DNA-reactive agents.

K Pavelic, T A Beerman, R J Bernacki
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引用次数: 4

Abstract

The combined application of DNA unwinding and strand-scission agents is a novel and potentially important approach to cancer therapy, based in part on mechanistic considerations of drug action. In order to evaluate this hypothesis a number of experiments were performed in which the cellular cytotoxicity of DNA reactive agents (ethidium bromide, adriamycin or cis-platinum) were evaluated alone and in combination with bleomycin, a strand-scission agent, using a number of different tumor cell systems in vitro. The results of these studies indicated that combinations of these agents were found to be much more effective than treatment with single drugs alone. This conclusion was warranted for the action of ethidium bromide followed by bleomycin with murine L1210 leukemia, melanoma B16-BL6 and human HeLa cells, and cis-platinum followed by bleomycin with L1210 and B16-BL6 cells. These data support previous findings in which synergistic growth inhibition of L1210 cells by ethidium bromide, followed by bleomycin was explained by a two-step mechanism; first, ethidium bromide introduces changes in DNA-conformation resulting in the facilitation of a second step in which bleomycin cleaves DNA more efficiently. Therefore, the rational use of combinations of DNA reactive agents based on mechanistic considerations should result with improved therapeutic regimens for the treatment of cancer.

体外应用dna活性药物联合化疗的疗效评价。
DNA解绕剂和链断裂剂的联合应用是一种新的和潜在的重要的癌症治疗方法,部分基于药物作用的机制考虑。为了评估这一假设,进行了许多实验,其中DNA反应剂(溴化乙啶、阿霉素或顺铂)的细胞毒性被单独评估,并与博来霉素(一种链断裂剂)联合使用,使用许多不同的体外肿瘤细胞系统。这些研究的结果表明,这些药物的组合被发现比单独使用单一药物治疗更有效。这一结论证实了溴化乙啶后博莱霉素对小鼠L1210白血病、黑色素瘤B16-BL6和人HeLa细胞的作用,顺铂后博莱霉素对L1210和B16-BL6细胞的作用。这些数据支持了先前的研究结果,即溴化乙啶和博来霉素对L1210细胞的协同生长抑制可以用两步机制来解释;首先,溴化乙锭引入DNA构象的变化,从而促进第二步,博来霉素更有效地切割DNA。因此,基于机理考虑的DNA反应剂组合的合理使用应该会改善治疗癌症的治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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