Baguley B C
Cancer Research Laboratory, University of Auckland Medical School, New Zealand.
Anticancer Drug Des. 1991 Feb;6(1):1-35.
Only a small proportion of DNA intercalators known today exhibit experimental anti-tumour activity and even fewer are useful clinically, raising the question of precisely what properties are necessary for an anti-cancer effect. A search for answers to this question has revealed a complex picture of how intercalators can interact with DNA and other macromolecules, which is the subject of this review. A description of some of the main intercalating anti-tumour agents is followed by a discussion of the principles of non-covalent drug-DNA interactions. The possible mechanisms by which DNA intercalation leads to anti-tumour activity are described and the concept of ternary complexes involving DNA, drug and DNA-binding proteins is developed. DNA topoisomerase II, which constitutes a prime target for intercalating anti-tumour drugs, is discussed in relation to ternary complex formation, tumour selectivity and drug resistance. Factors affecting the transport of drugs into and within cells are also discussed. An emphasis is placed in this review on guiding principles which may facilitate the design of novel or more effective agents in the future.
在如今已知的DNA嵌入剂中,只有一小部分表现出实验性抗肿瘤活性,而临床上可用的更少,这就引出了一个问题:抗癌效应究竟需要哪些特性。对这个问题答案的探寻揭示了嵌入剂与DNA及其他大分子相互作用的复杂情况,这也是本综述的主题。在描述了一些主要的嵌入型抗肿瘤药物之后,讨论了非共价药物 - DNA相互作用的原理。阐述了DNA嵌入导致抗肿瘤活性的可能机制,并提出了涉及DNA、药物和DNA结合蛋白的三元复合物概念。作为嵌入型抗肿瘤药物主要靶点的DNA拓扑异构酶II,将从三元复合物形成、肿瘤选择性和耐药性方面进行讨论。还讨论了影响药物进入细胞及在细胞内转运的因素。本综述重点强调了一些指导原则,这些原则可能有助于未来新型或更有效药物的设计。