Abstract
Since the discovery of 8-OH-dG formation, various aspects of oxidative DNA damage have been studied. For example, 2-OH-dA and a glyoxal-dG adduct were discovered as new types of oxidative DNA damage; 2-OH-dATP was found to induce mutations and to be a good substrate of a nucleotide sanitization enzyme, the MTH1 protein; and efforts were continued to establish standard methodologies for 8-OH-dG analyses in urine and cellular DNA. By these studies, we found solid chemistry-based approaches were often useful to clarify the biological phenomena.
MeSH terms
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8-Hydroxy-2'-Deoxyguanosine
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Adenosine Triphosphate / analogs & derivatives*
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Adenosine Triphosphate / metabolism
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Adenosine Triphosphate / pharmacology
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Bacterial Proteins / metabolism
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Chromatography, High Pressure Liquid
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DNA Adducts / analysis
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DNA Damage*
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DNA Repair*
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DNA, Bacterial / genetics
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DNA-Directed DNA Polymerase / metabolism
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Deoxyguanosine / analogs & derivatives*
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Deoxyguanosine / metabolism
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Deoxyguanosine / urine
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Enzyme-Linked Immunosorbent Assay
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Escherichia coli / genetics
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Free Radicals
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Humans
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Mutagenesis*
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Nucleosides / chemistry*
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Oxidation-Reduction
Substances
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2-hydroxydeoxyadenosine triphosphate
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Bacterial Proteins
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DNA Adducts
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DNA, Bacterial
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Free Radicals
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Nucleosides
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8-Hydroxy-2'-Deoxyguanosine
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Adenosine Triphosphate
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DNA-Directed DNA Polymerase
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Deoxyguanosine