Small-molecule inhibitors of DNA damage-repair pathways: an approach to overcome tumor resistance to alkylating anticancer drugs

被引:1
|
作者
Srinivasan, Ajay [1 ]
Gold, Barry [1 ]
机构
[1] Univ Pittsburgh, Dept Pharmaceut Sci, Pittsburgh, PA 15261 USA
关键词
BASE EXCISION-REPAIR; ADENOMATOUS POLYPOSIS-COLI; HUMAN APURINIC/APYRIMIDINIC ENDONUCLEASE-1; POLYMERASE-BETA INHIBITOR; EMBRYONIC STEM-CELLS; CROSS-LINK REPAIR; LIGASE-I; FLAP ENDONUCLEASE-1; PARP INHIBITORS; AP ENDONUCLEASE;
D O I
10.4155/FMC.12.58
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A major challenge in the future development of cancer therapeutics is the identification of biological targets and pathways, and the subsequent design of molecules to combat the drug-resistant cells hiding in virtually all cancers. This therapeutic approach is justified based upon the limited advances in cancer cures over the past 30 years, despite the development of many novel chemotherapies and earlier detection, which often fail due to drug resistance. Among the various targets to overcome tumor resistance are the DNA repair systems that can reverse the cytotoxicity of many clinically used DNA-damaging agents. Some progress has already been made but much remains to be done. We explore some components of the DNA-repair process, which are involved in repair of alkylation damage of DNA, as targets for the development of novel and effective molecules designed to improve the efficacy of existing anticancer drugs.
引用
收藏
页码:1093 / 1111
页数:19
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