突变
DNA修复
基因
突变
癌变
点突变
癌症研究
作者
Mia Petljak,John Maciejowski
出处
期刊:DNA Repair
[Elsevier BV]
日期:2020-10-01
卷期号:94: 102905-102905
被引量:45
标识
DOI:10.1016/j.dnarep.2020.102905
摘要
The APOBEC family of cytidine deaminases has been proposed to represent a major enzymatic source of mutations in cancer. Here, we summarize available evidence that links APOBEC deaminases to cancer mutagenesis. We also highlight newly identified human cell models of APOBEC mutagenesis, including cancer cell lines with suspected endogenous APOBEC activity and a cell system of telomere crisis-associated mutations. Finally, we draw on recent data to propose potential causes of APOBEC misregulation in cancer, including the instigating factors, the relevant mutator(s), and the mechanisms underlying generation of the genome-dispersed and clustered APOBEC-induced mutations.
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