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Oxidative DNA damage background estimated by a system model of base excision repair
Journal article   Open access   Peer reviewed

Oxidative DNA damage background estimated by a system model of base excision repair

Bahrad A Sokhansanj, David M Wilson and Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)
Free radical biology & medicine, v 37(3), pp 422-427
01 Aug 2004
PMID: 15223076
url
https://digital.library.unt.edu/ark:/67531/metadc1406017/View

Abstract

Human DNA can be damaged by natural metabolism through free radical production. It has been suggested that the equilibrium between innate damage and cellular DNA repair results in an oxidative DNA damage background that potentially contributes to disease and aging. Efforts to quantitatively characterize the human oxidative DNA damage background level, based on measuring 8-oxoguanine lesions as a biomarker, have led to estimates that vary over three to four orders of magnitude, depending on the method of measurement. We applied a previously developed and validated quantitative pathway model of human DNA base excision repair, integrating experimentally determined endogenous damage rates and model parameters from multiple sources. Our estimates of at most 100 8-oxoguanine lesions per cell are consistent with the low end of data from biochemical and cell biology experiments, a result robust to model limitations and parameter variation. Our findings show the power of quantitative system modeling to interpret composite experimental data and make biologically and physiologically relevant predictions for complex human DNA repair pathway mechanisms and capacity.

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20 citations in Scopus

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Collaboration types
Domestic collaboration
Web of Science research areas
Biochemistry & Molecular Biology
Endocrinology & Metabolism
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