Emerging Roles of RAD52 in Genome Maintenance
Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA
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Author to whom correspondence should be addressed.
Cancers 2019, 11(7), 1038; https://doi.org/10.3390/cancers11071038
Received: 21 June 2019 / Revised: 17 July 2019 / Accepted: 18 July 2019 / Published: 23 July 2019
(This article belongs to the Special Issue Current Understanding of RAD52 Functions: Fundamental and Therapeutic Insights)
The maintenance of genome integrity is critical for cell survival. Homologous recombination (HR) is considered the major error-free repair pathway in combatting endogenously generated double-stranded lesions in DNA. Nevertheless, a number of alternative repair pathways have been described as protectors of genome stability, especially in HR-deficient cells. One of the factors that appears to have a role in many of these pathways is human RAD52, a DNA repair protein that was previously considered to be dispensable due to a lack of an observable phenotype in knock-out mice. In later studies, RAD52 deficiency has been shown to be synthetically lethal with defects in BRCA genes, making RAD52 an attractive therapeutic target, particularly in the context of BRCA-deficient tumors.
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Keywords:
RAD52; RNA:DNA hybrids; R-loops; DNA repair; double-strand break repair; BRCA1; BRCA2; RAD51; synthetic lethality; genome instability
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MDPI and ACS Style
Jalan, M.; Olsen, K.S.; Powell, S.N. Emerging Roles of RAD52 in Genome Maintenance. Cancers 2019, 11, 1038. https://doi.org/10.3390/cancers11071038
AMA Style
Jalan M, Olsen KS, Powell SN. Emerging Roles of RAD52 in Genome Maintenance. Cancers. 2019; 11(7):1038. https://doi.org/10.3390/cancers11071038
Chicago/Turabian StyleJalan, Manisha; Olsen, Kyrie S.; Powell, Simon N. 2019. "Emerging Roles of RAD52 in Genome Maintenance" Cancers 11, no. 7: 1038. https://doi.org/10.3390/cancers11071038
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