Mitotic homologous recombination maintains genomic stability and suppresses tumorigenesis Journal Article


Authors: Moynahan, M. E.; Jasin, M.
Article Title: Mitotic homologous recombination maintains genomic stability and suppresses tumorigenesis
Abstract: Mitotic homologous recombination promotes genome stability through the precise repair of DNA double-strand breaks and other lesions that are encountered during normal cellular metabolism and from exogenous insults. As a result, homologous recombination repair is essential during proliferative stages in development and during somatic cell renewal in adults to protect against cell death and mutagenic outcomes from DNA damage. Mutations in mammalian genes encoding homologous recombination proteins, including BRCA1, BRCA2 and PALB2, are associated with developmental abnormalities and tumorigenesis. Recent advances have provided a clearer understanding of the connections between these proteins and of the key steps of homologous recombination and DNA strand exchange. © 2010 Macmillan Publishers Limited. All rights reserved.
Keywords: unclassified drug; mutation; review; neoplasms; cell proliferation; mitosis; mammalia; animals; cell death; dna damage; homologous recombination; dna repair; models, biological; gene function; cell renewal; brca1 protein; brca2 protein; carcinogenesis; cancer inhibition; recombination, genetic; genomic instability; dna breaks, double-stranded; dna breaks, single-stranded; genome; cell metabolism; mutagenesis; palb2 protein; dna strand
Journal Title: Nature Reviews Molecular Cell Biology
Volume: 11
Issue: 3
ISSN: 1471-0072
Publisher: Nature Publishing Group  
Date Published: 2010-03-01
Start Page: 196
End Page: 207
Language: English
DOI: 10.1038/nrm2851
PUBMED: 20177395
PROVIDER: scopus
PMCID: PMC3261768
DOI/URL:
Notes: --- - "Cited By (since 1996): 26" - "Export Date: 20 April 2011" - "CODEN: NRMCB" - "Source: Scopus"
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  1. Mary Ellen Moynahan
    105 Moynahan
  2. Maria Jasin
    249 Jasin