Direct and Hydrogen Peroxide-Induced Chromium(V) Oxidation of Deoxyribose in Single-Stranded and Double-Stranded Calf Thymus DNA
- 1 December 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in Chemical Research in Toxicology
- Vol. 10 (12) , 1397-1406
- https://doi.org/10.1021/tx970135r
Abstract
Oxidative DNA damage by a model Cr(V) complex, [CrO(ehba)2]-, with and without added H2O2, was investigated for the formation of base and sugar products derived from C1‘, C4‘, and C5‘ hydrogen atom abstraction mechanisms. EPR studies with 5,5-dimethylpyrroline N-oxide (DMPO) have shown that Cr(V)-ehba alone can oxidize the spin trap via a direct chromium pathway, whereas reactions of Cr(V)-ehba in the presence of H2O2 generated the hydroxyl radical. Direct (or metal-centered) Cr(V)-ehba oxidation of single-stranded (ss) and double-stranded (ds) calf thymus DNA demonstrated the formation of thiobarbituric acid-reactive species (TBARS) and glycolic acid in an O2-dependent manner, consistent with abstraction of the C4‘ H atom. A minor C1‘ H atom abstraction mechanism was also observed for direct Cr(V) oxidation of DNA, but no C5‘ H atom abstraction product was observed. Direct Cr(V) oxidation of ss- and ds-DNA also caused the release of all four nucleic acid bases with a preference for the pyrimidines cytosine and thymine in ds-DNA, but no base release preference was observed in ss-DNA. This base release was O2-independent and could not be accounted for by the H atom abstraction mechanisms in this study. Reaction of Cr(V)-ehba with H2O2 and DNA yielded products consistent with all three DNA oxidation pathways measured, namely, C1‘, C4‘, and C5‘ H atom abstractions. Cr(V)-ehba and H2O2 also mediated a nonpreferential release of DNA bases with the exception of the oxidatively sensitive purine, guanine. Direct and H2O2-induced Cr(V) DNA oxidation had opposing substrate preferences, with direct Cr(V) oxidation favoring ss-DNA while H2O2-induced Cr(V) oxidative damage favored ds-DNA. These results may help explain the carcinogenic mechanism of chromium(VI) and serve to highlight the differences and similarities in DNA oxidation between high-valent chromium and oxygen-based radicals.Keywords
This publication has 16 references indexed in Scilit:
- Chemical Mechanism of DNA Scission by (1,10-Phenanthroline)copper. Carbonyl Oxygen of 5-Methylenefuranone Is Derived from WaterJournal of the American Chemical Society, 1997
- Identification of the Oxidized Products Formed upon Reaction of Chromium(V) with Thymidine NucleotidesJournal of the American Chemical Society, 1996
- The formation of both apurinic/apyrimidinic sites and single-strand breaks by chromate and glutathione arises from attack by the same single reactive species and is dependent on molecular oxygenCarcinogenesis: Integrative Cancer Research, 1995
- Thymidine-specific depyrimidination of DNA by oxopolypyridylruthenium(IV) complexesJournal of the American Chemical Society, 1993
- New insight into the mechanism of base propenal formation during bleomycin-mediated DNA degradationJournal of the American Chemical Society, 1992
- Is there a role for reactive oxygen species in the mechanism of chromium(VI) carcinogenesis?Chemical Research in Toxicology, 1991
- Conversion of superoxide generated by polymorphonuclear leukocytes to hydroxyl radical: A direct spectrophotometric detection system based on degradation of deoxyriboseFree Radical Biology & Medicine, 1989
- Nuclease activity of 1,10-phenanthroline-copper ion. Chemistry of deoxyribose oxidationJournal of the American Chemical Society, 1987
- Microsomal reduction of the carcinogen chromate produces chromium(V)Journal of the American Chemical Society, 1982
- Cleavage of double helical DNA by methidium-propyl-EDTA-iron(II)Journal of the American Chemical Society, 1982