Redox Regulation of DNA Repair: Implications for Human Health and Cancer Therapeutic Development

dc.contributor.authorLuo, Meihua
dc.contributor.authorHe, Hongzhen
dc.contributor.authorKelley, Mark R.
dc.contributor.authorGeorgiadis, Millie M.
dc.date.accessioned2014-07-29T19:49:37Z
dc.date.available2014-07-29T19:49:37Z
dc.date.issued2010-06
dc.description.abstractRedox reactions are known to regulate many important cellular processes. In this review, we focus on the role of redox regulation in DNA repair both in direct regulation of specific DNA repair proteins as well as indirect transcriptional regulation. A key player in the redox regulation of DNA repair is the base excision repair enzyme apurinic/apyrimidinic endonuclease 1 (APE1) in its role as a redox factor. APE1 is reduced by the general redox factor thioredoxin, and in turn reduces several important transcription factors that regulate expression of DNA repair proteins. Finally, we consider the potential for chemotherapeutic development through the modulation of APE1's redox activity and its impact on DNA repair.en_US
dc.identifier.citationLuo, M., He, H., Kelley, M. R., & Georgiadis, M. M. (2010). Redox regulation of DNA repair: implications for human health and cancer therapeutic development. Antioxidants & redox signaling, 12(11), 1247-1269.en_US
dc.identifier.urihttps://hdl.handle.net/1805/4795
dc.language.isoen_USen_US
dc.subjectDNA repairen_US
dc.subjectAPE1en_US
dc.subjectcanceren_US
dc.titleRedox Regulation of DNA Repair: Implications for Human Health and Cancer Therapeutic Developmenten_US
dc.typeArticleen_US
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