AlkB
DNA修复
DNA损伤
基底切除修复术
核苷酸切除修复
癌症研究
生物
鸟嘌呤
DNA
癌症
O-6-甲基鸟嘌呤-DNA甲基转移酶
癌细胞
烷基化
甲基转移酶
遗传学
生物化学
基因
核苷酸
甲基化
催化作用
作者
Yuan-Ching Peng,Huadong Pei
出处
期刊:Journal of Zhejiang University-science B
[Springer Nature]
日期:2021-01-01
卷期号:22 (1): 47-62
被引量:17
标识
DOI:10.1631/jzus.b2000344
摘要
Alkylated DNA lesions, induced by both exogenous chemical agents and endogenous metabolites, represent a major form of DNA damage in cells. The repair of alkylation damage is critical in all cells because such damage is cytotoxic and potentially mutagenic. Alkylation chemotherapy is a major therapeutic modality for many tumors, underscoring the importance of the repair pathways in cancer cells. Several different pathways exist for alkylation repair, including base excision and nucleotide excision repair, direct reversal by methyl-guanine methyltransferase (MGMT), and dealkylation by the AlkB homolog (ALKBH) protein family. However, maintaining a proper balance between these pathways is crucial for the favorable response of an organism to alkylating agents. Here, we summarize the progress in the field of DNA alkylation lesion repair and describe the implications for cancer chemotherapy.
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