甲基转移酶
化疗
癌症研究
前药
DNA甲基转移酶
O-6-甲基鸟嘌呤-DNA甲基转移酶
DNA损伤
DNA修复
生物
DNA
药理学
化学
生物化学
遗传学
甲基化
作者
Guizhi Sun,Lu Zhao,Rugang Zhong,Yongzhen Peng
出处
期刊:Future Medicinal Chemistry
[Newlands Press Ltd]
日期:2018-08-01
卷期号:10 (16): 1971-1996
被引量:32
标识
DOI:10.4155/fmc-2018-0069
摘要
The DNA repair protein, O 6 -methylguanine DNA methyltransferase (MGMT), can confer resistance to guanine O 6 -alkylating agents. Therefore, inhibition of resistant MGMT protein is a practical approach to increase the anticancer effects of such alkylating agents. Numerous small molecule inhibitors were synthesized and exhibited potential MGMT inhibitory activities. Although they were nontoxic alone, they also inhibited MGMT in normal tissues, thereby enhancing the side effects of chemotherapy. Therefore, strategies for tumor-specific MGMT inhibition have been proposed, including local drug delivery and tumor-activated prodrugs. Over-expression of MGMT in hematopoietic stem cells to protect bone marrow from the toxic effects of chemotherapy is also a feasible selection. The future prospects and challenges of MGMT inhibitors in cancer chemotherapy were also discussed.
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