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DNA as a target for anticancer compounds: methods to determine the mode of binding and the mechanism of action

机译:DNA作为抗癌化合物的靶标:确定结合方式和作用机理的方法

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摘要

Small molecules that bind to DNA are extremely useful as biochemical tools for the visualization of DNA both in vitro and inside the cell. Additionally, the clinical significance of DNA-binding compounds can hardly be overstated, as many anticancer regimens include a compound that binds to and/or modifies DNA. Although many of the important DNA-binding anticancer drugs were discovered in phenotypic, cell-based screens, in vitro experiments have been developed that enable a precise determination of how a compound interacts with DNA. This review provides a summary of the assays that should be performed when it is suspected that DNA may be a target for a given small molecule. A battery of in vitro assays readily distinguishes between DNA intercalation, DNA groove binding, and the inhibition of topoisomerases. Further cell-based investigations can implicate a direct effect of a compound on DNA within the cell. Together, these assays are powerful tools to determine the mechanism of previously discovered molecules, and will be crucial to the discovery of the next generation of DNA-binding anticancer drugs.
机译:与DNA结合的小分子作为生化工具极其有用,可用于在体外和细胞内可视化DNA。另外,由于许多抗癌方案都包括与DNA结合和/或修饰的化合物,因此与DNA结合的化合物的临床意义很难被夸大。尽管在基于细胞表型的筛选中发现了许多重要的与DNA结合的抗癌药物,但已经开展了体外实验,可以精确确定化合物与DNA的相互作用方式。这篇综述总结了当怀疑DNA可能是给定小分子的靶标时应进行的测定的摘要。一系列的体外测定很容易区分DNA嵌入,DNA凹槽结合和拓扑异构酶抑制。进一步的基于细胞的研究可能暗示化合物对细胞内DNA的直接作用。总之,这些测定法是确定先前发现的分子机制的有力工具,对于发现下一代DNA结合抗癌药至关重要。

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