抗癌药物的脱氧核糖核酸(DNA)相互作用

S. Alotaibi, A. Momen
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引用次数: 21

摘要

脱氧核糖核酸(DNA)是控制细胞中发生的所有化学变化的生命分子。药物与DNA的相互作用是药物发现和药物开发过程中生物学研究中最重要的方面之一。此外,了解合理设计化疗药物的特定靶点是设计可用于治疗肿瘤疾病的分子的基本因素。观察药物- dna相互作用的前后标志为阐明相互作用机制提供了良好的证据。此外,这种相互作用可用于药物的定量和靶向DNA的新药的测定。这些方法可以为合理的药物设计提供新的见解,并有助于进一步了解抗癌药物与DNA的相互作用机制。本章的目的是提供几个抗癌药物、DNA相互作用和相互作用机制的例子,以了解几个相互作用因素对抗癌药物与DNA相互作用的能力和选择性的影响。此外,还讨论了检测和评价抗癌药物与DNA相互作用的不同实验和理论方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anticancer Drugs’ Deoxyribonucleic Acid (DNA) Interactions
The deoxyribonucleic acid (DNA) is the molecule of life that controls all the chemical changes that take place in cells. The interaction of drugs with DNA is among the most important aspects of biological studies in drug discovery and pharmaceutical development processes. Moreover, the knowledge of specific targets in rational design of chemotherapeutics is a fundamental factor, principally, for the design of molecules that can be used in the treatment of oncologic diseases. Observing the pre- and postsigns of drug-DNA interaction provides good evidence for the interaction mechanism to be elucidated. Also, this interaction could be used for the quantification of drugs and for the determination of new drugs targeting DNA. Approaches can provide new insight into rational drug design and would lead to further understanding of the interaction mechanism between anticancer drugs and DNA. The intention of this chapter is to provide several examples of anticancer drugs, DNA interaction, and the mechanisms of interaction in order to understand the influence of several interaction factors in the capacity and selectivity of the anticancer drugs to interact with DNA. In addition, different experimental and theoretical approaches to detect and to evaluate the anticancer drugs’ interactions with DNA were also discussed.
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