Molecular origins of APOBEC-associated mutations in cancer.

DNA Repair (Amst)

Molecular Biology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA. Electronic address:

Published: October 2020

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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7494591PMC
http://dx.doi.org/10.1016/j.dnarep.2020.102905DOI Listing

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