8-Oxo-7,8-dihydroguanine and 8-oxo-7,8-dihydro-2′-deoxyguanosine levels in human urine do not depend on diet

References

• Cheng K.C., Cahill D.S., Kasai H., Nishimura S., Loeb L.A. 8-Hydroxyguanine, an abundant form of oxidative DNA damage, causes G-T and A-C substitutions. Journal of Biological Chemistry 1992; 267: 166–172
   PubMed Web of Science ®Google Scholar
• Feig D.I., Reid T.M., Loeb L.A. Reactive oxygen species in tumorigenesis. Cancer Research 1994; 54: 1890–1894
   PubMed Web of Science ®Google Scholar
• Floyd R.A. The role of 8-hydroxyguanine in carcinogenesis. Carcinogenesis 1990; 11: 1447–1450
   PubMed Web of Science ®Google Scholar
• Olinski R., Zastaswny T.H., Budzbon J., Skokowski J., Zegarski W., Dizdaroglu M. DNA base modifications in chromatin of human cancerous tissues. FEBS Letters 1992; 193: 193–198
   Google Scholar
• Shigenaga M.K., Gimeno C.J., Ames B.N. Urinary 8-hydroxy-2′-deoxyguanosine as a biological marker of in vivo oxidative DNA damage. Proceedings of the National Academy of Science USA 1992; 86: 9697–9701
   Google Scholar
• Suzuki J., Inoue Y., Suzuki S. Changes in the urinary excretion level of 8-hydroxyguanine by exposure to reactive oxygen-generating substances. Free Radicals in Biology and Medicine 1995; 18: 431–435
   PubMed Web of Science ®Google Scholar
• Loft S., Poulsen H.E. Markers of oxidative damage to DNA: antioxidants and molecular damage. Methods in Enzymology 1995; 300: 166–184
   Google Scholar
• Cooke M.S., Evans M.D., Herbert K.E., Lunec J. Urinary 8-oxo-2′-deoxyguanosine—source, significance and supplements. Free Radical Research 2000; 32: 381–397
   PubMed Web of Science ®Google Scholar
• Loft S., Poulsen H.E. Estimation of oxidative DNA damage in man from urinary excretion of repair products. Acta Biochimica Polonica 1998; 45: 133–144
   PubMed Web of Science ®Google Scholar
• Girard P.M., Boiteux S. Repair of oxidized DNA bases in the yeast Saccharomyces cerevisiae. Biochimie 1997; 79: 559–566
   PubMed Web of Science ®Google Scholar
• Dianov G., Bischoff C., Piotrowski J., Bohr V.A. Repair pathways for processing of 8-oxoguanine in DNA by mammalian cell extracts. Journal of Biological Chemistry 1998; 273: 33811–33816
   PubMed Web of Science ®Google Scholar
• Radicella J.P., Dherin C., Desmaze M.S., Fox S., Boiteux S. Cloning and characterization of hOGG1, a human homolog of the OGG1 gene of Saccharomyces cerevisiae. Proceedings of the National Academy of Science USA 1997; 94: 8010–8015
   PubMed Web of Science ®Google Scholar
• Hazra T.K., Izumi T., Maidt L., Floyd R.A., Sancar M. The presence of two distinct 8-oxoguanine repair enzymes in human cells: their potential complementary roles in preventing mutation. Nucleic Acid Research 1998; 26: 5116–5122
   PubMed Web of Science ®Google Scholar
• Helbock H.J., Beckman K.B., Shigenaga M.K., Walter P.B., Woodall A.A., Yeo H.C., Ames B.N. DNA oxidation matters: the HPLC-electrochemical detection assay of 8-oxo-deoxyguanosine and 8-oxoguanine. Proceedings of the National Academy of Science USA 1998; 95: 288–293
   PubMed Web of Science ®Google Scholar
• Ravanat J.-L., Guicherd P., Tuce Z., Cadet J. Simultaneous determination of five oxidative DNA lesions in human urine. Chemical Research in Toxicology 1999; 12: 802–808
   PubMed Web of Science ®Google Scholar
• Ravanat J.-L., Duretz B., Guiler A., Douki T., Cadet J. Isotope dilution high-performance liquid chromatography-electrospray tandem mass spectrometry assay for the measurement of 8-oxo-7,8-dihydro-2′-deoxyguanosine in biological samples. Journal of Chromatography B: Biomedical Sciences and Applications 1998; 715: 349–356
   PubMed Web of Science ®Google Scholar
• Weimann A., Belling D., Poulsen H.E. Measurement of 8-oxo-2′-deoxyguanosine in DNA and human urine by high performance liquid chromatography-electrospray tandem mass spectrometry. Free Radicals in Biology and Medicine 2001; 30: 757–764
   PubMed Web of Science ®Google Scholar
• Park E.-M., Shigenaga M.K., Degan P., Korn T.S., Kitzler J.W., Wehr C.M., Kolachana P., Ames B.N. Assay of excised oxidative DNA lesions: isolation of 8-oxoguanine and its nucleoside derivatives from biological fluids with a monoclonal antibody column. Proceedings of the National Academy of Science USA 1992; 89: 3375–3379
   PubMed Web of Science ®Google Scholar
• Dizdaroglu M. Chemical determination of oxidative DNA damage by gas chromatography-mass spectrometry. Methods in Enzymology 1994; 243: 3–16
   Google Scholar
• Helbock H.J., Thompson J., Yeo H., Ames B.N. N2-methyl-8-oxoguanine: a tRNA urinary metabolite—role of xanthine oxidase. Free Radicals in Biology and Medicine 1996; 20: 475–481
   PubMedGoogle Scholar
• Pak N., Donoso G., Tagle M.A. Allantoin excretion in the rat. British Journal of Nutrition 1973; 30: 107–112
   PubMedGoogle Scholar
• Savaiano D.A., Ho C.Y., Chu V., Clifford A.J. Metabolism of orally and intravenously administered purines in rats. Journal of Nutrition 1980; 110: 1793–1804
   PubMed Web of Science ®Google Scholar
• Brule D., Sarwar G., Savoie L., Campbell J., van Zeggelaar M. Differences in uricogenic effects of purine bases, nucleosides and nucleotides in rats. Journal of Nutrition 1998; 118: 780–786
   Google Scholar
• Chen Q., Fischer A., Reagan J.D., Yan L.J., Ames B.N. Oxidative DNA damage and senescence of human diploid fibroblast cells. Proceedings of the National Academy of Science USA 1995; 92: 4337–4341
   PubMed Web of Science ®Google Scholar
• Spivak G., Hanawalt P.C. Fine structure mapping of DNA repair within a 100 kb genomic region in Chinese hamster ovary cells. Mutation Reasearch 1996; 350: 207–216
   PubMedGoogle Scholar
• la Page F., Gentil A., Sarasin A. Repair and mutagenesis survery of 8-hydroxyguanine in bacteria and human cells. Biochimie 1999; 81: 147–153
   PubMedGoogle Scholar
• Minowa O., Arai T., Hirano M., Monden M., Nakai S., Fukuda M., Itoh M., Takano H., Hippou Y., Aburatani H., Masamura K., Nohmi T., Nishimura S., Noda T. Mmh/Ogg1 gene inactivation results in accumulation of 8-hydroxyguanine in mice. Proceedings of the National Academy of Science USA 2000; 97: 4156–4161
   PubMed Web of Science ®Google Scholar
• Klungland A., Rosewell I., Hollenbach S., Larsen E., Daly G., Epe B., Seeberg E., Lindahl T., Barnes D.E. Accumulation of premutagenic DNA lesions in mice defective in removal of oxidative base damage. Proceedings of the National Academy of Science USA 1999; 96: 13300–13305
   PubMed Web of Science ®Google Scholar
• la Page F., Klungland A., Barnes D.E., Sarasin A., Boiteux S. Transcription coupled repair of 8-oxoguanine in murine cells: the Ogg1 protein is required for repair in nontranscribed sequences but not in transcribed sequences. Proceedings of the National Academy of Science USA 2000; 97: 8397–8402
   PubMedGoogle Scholar
• Lindahl T., Wood R.D. Quality control by DNA repair. Science 1999; 286: 1897–1905
   PubMed Web of Science ®Google Scholar