| Literature DB >> 33087261 |
Abstract
DNA mismatch repair (MMR) maintains genomic stability primarily by correcting replication errors. Defects in MMR lead to cancers and cause resistance to many chemotherapeutic drugs. Emerging evidence reveals that MMR is coupled with replication and precisely regulated in the context of chromatin; strikingly, tumors defective in MMR are highly responsive to immune checkpoint blockade therapy. As a tribute to Dr. Samuel Wilson for his many scientific contributions to the field of DNA repair and his leadership as Editor-in-Chief of the journal DNA Repair, we summarize recent developments in research on MMR at the chromatin level, its implications for tumorigenesis, and its therapeutic potential.Entities:
Keywords: Cancer therapy; Chromatin structure; Mimsatch repair; Replication fork
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Year: 2020 PMID: 33087261 PMCID: PMC7583346 DOI: 10.1016/j.dnarep.2020.102918
Source DB: PubMed Journal: DNA Repair (Amst) ISSN: 1568-7856