Monitoring urinary excretion of 5-hydroxymethyluracil for assessment of oxidative DNA damage and repair

References

• Ames B. N., Shigenaga M. K., Hagen T. M. Oxidants, antioxidants, and the degenerative diseases of ageing. Proceedings of the National. Academy of Sciences, USA 1993; 90: 7915–7922
   PubMed Web of Science ®Google Scholar
• Bergtold D. S., Simic M. G. Urine biomarkers for oxidative DNA damage. Oxygen Radicals in Biology and Medicine, M. G. Simic, K. A. Taylor, J. F. Ward, C. von Sonntag. Plenum Press, New York 1988; 483–490
   Google Scholar
• Bjelland S., Birkeland N. K., Benneche T, Volden G., Seeberg E. DNA glycosylase activities for thymine residues oxidized in the methyl group are functions of the AlkA enzyme in Escherichia coli. Journal of Biological Chemistry 1994; 269: 30489–30495
   PubMed Web of Science ®Google Scholar
• Boteux S., Gajewski E., Laval J., Dizdaroglou M. Substrate specificity of the Escherichia coli Fpg protein (formamidopyrimidine-DNA giycosylase): excision of purine lesions in DNA produced by ionizing radiation or photosensitization. Biochemistry 1992; 31: 106–110
   PubMed Web of Science ®Google Scholar
• Boorstein R. J., Levy D. D., Teebor G. W. 5-Hydroxymethyluracil-DNA glycosylase activity may be a ditferentiated mammalian function. Mutation Research 1987; 183: 257–263
   PubMedGoogle Scholar
• Cadet J. DNA damage caused by oxidation, deamination, ultraviolet radiation and photoexcited psoralens. In DNA Adducts: Identification and Biological Significance, K. Hemminki, A. Dipple, D. E. G. Shuker, F. F. Kadlubar, D. Segerbäck, H. Bartsch. International Agency for Research on Cancer, Lyon 1994; 245–276, IARC Scientific Publication No. 125
   Google Scholar
• Cannon-Carlson S. V., Gokhale H., Teebor G. W. Purification and characterization of 5-hydroxymethyluraci-DNA giycosylase from calf thymus. Journal of Biological Chemistry 1989; 264: 13306–13312
   PubMed Web of Science ®Google Scholar
• Cao E. H., Wang J.J. Oxidative damage to DNA levels of thymine glycol and thymidine glycol in neoplastic human urines. Carcinogenesis 1993; 14: 1359–1362
   PubMed Web of Science ®Google Scholar
• Cathcart R., Schwers E., Saul R. L., Ames B. N. Thymine glycol and thymidine glycol in human and rat urine: a possible assay for oxidative DNA damage. Proceedings of the National Academy of Sciences, USA 1984; 81: 5632–5637
   Web of Science ®Google Scholar
• Cline R. E., Fink R. M., Fink K. Synthesis of 5′-substituted pyrimidines via formaldehyde addition. Journal of the American Chemical Society 1959; 81: 2521–2527
   Web of Science ®Google Scholar
• Demple B., Harrison L. Repair of oxidative damage to DNA. Annual Review of Biochemistry 1994; 63: 915–94
   PubMed Web of Science ®Google Scholar
• Dixon W. J., Brown M. B., Engelman L., Jenrioh N. I. EMDP. Statistical Software Manual. University of California Press, Los Angeles 1990
   Google Scholar
• Djuric Z., Heilbrun L. K., Reading B. A., Boomer A., Valeriote F. A., Marnno S. Effects of a low-fat diet on levels of oxidative damage to DNA in human peripheral nucleated blood cells. Journal of the National Cancer Institute 1991; 83: 766–769
   PubMedGoogle Scholar
• Djuric Z., Lu M. H., Lewis S. M., Luongo D. A., Chen X. W., Heilbrun L. K., Readng B. A., Duffy P. H., Hart R. W. Oxidative DNA damage levels in rats fed low-fat, high fat, or caloric-restricted diets. Toxicology and Applied Pharmacology 1992; 115: 156–160
   PubMed Web of Science ®Google Scholar
• Faure H., Incardna M. F., Boulet C., Cadet J., Ducros V., Favier A. Gas chromatographic-mass spectrometric determination of 5-hydroxymethyluracil in human urine by stable isotope dilution. Journal of Chromatography 1993; 616: l–7
   Web of Science ®Google Scholar
• Friedberg E. C., Ganesan A. K., Minton K. N-glycosidase activity in extracts of Bacillus subtilis and its inhibition after affection with bacteriophage PBS2. Journal of Vuology 1978; 16: 315–321
   Google Scholar
• Hayakawa H., Taketom A., Sakumi K., Kuwano M., Sekiguch M. Generation and elimination of 8-oxo-7,8-dihyd-2′deoxyguanosine 5′-triphosphate, a mutagenic substrate for DNA synthesis, in human cells. Biochemistry 1995; 34: 89–95
   PubMed Web of Science ®Google Scholar
• Hollstein M. C., Brooks P., Linn S., Ames B. N. Hydroxymethyluracil DNA glycosylase in mammalian cells. Proceedings of the National Academy of Sciences, USA 1984; 81: 4003–4007
   PubMed Web of Science ®Google Scholar
• Incardona M. F., Biawchin F., Favier A., Cadet J. Measurement of oxidized nucleobases and nucleosides in human urine by using a GC/MS assay in the selective ion monitoring mode. Analysis of Free Radicals in Biological Systems, A. Favier, J. Cadet, E. Kalyanaraman, M. Fontecave, J. L. Pierre. Birkhausen, Basel 1995; 249–260
   Google Scholar
• Kaufman E. R. Induction of sister chromatid exchanges by the thymidine analog Shydroxymethyldeoxyridine. Somatic Cell and Molecular Genetics 1989; 15: 563–568
   PubMedGoogle Scholar
• Lindahl T. Instability and decay of the primary structure of DNA. Nature 1993; 362: 709–715
   PubMed Web of Science ®Google Scholar
• Loft S., Vistisen K., Ewertz M., Tjonneland A., Overyad K., Poulsen H. E. Oxidative DNA damage estimated by & hydroxydeoxyguanosine excretion in humans: influence of smoking, gender and body mass index. Carcinogenesis 1992; 13: 2241–2247
   PubMed Web of Science ®Google Scholar
• Loft S., Fisher-Nelsen A., Jeding I. B., Visnsen K., Poulsen H. E. 8 Hydroxydeoxyguanosine as a urinary biomarker of oxidative DNA damage. Journal of Toxicology and Environmental Health 1993; 40: 391–404
   PubMed Web of Science ®Google Scholar
• Loft S., Astrup A., Buemann B., Poulsen H. E. Oxidative DNA damage correlates with oxygen consumption in humans. FASEB Journal 1994; 8: 534–537
   PubMed Web of Science ®Google Scholar
• Mauns D. M. Identification of hydroxyl radical-induced lesions in DNA base structure: biomarkers with a putative link to cancer development. Journal of Toxicology and Environmental Health 1993; 40: 247–261
   PubMedGoogle Scholar
• Marnett L. J., Burcham P. C. Endogenous DNA adducts: potential and paradox. Chemical Research in Toxicology 1993; 6: 771–785
   PubMed Web of Science ®Google Scholar
• Neter J., Wasserman W., Kutner M. H. Applied Linear Statistical Methods. Irwin, Homewood, IL 1990
   Google Scholar
• Ounski R., Zastawny T., Budzbon J., Skokowski J., Zegarski W., Dizdaroglu M. DNA base modifications in chromatin of human cancerous tissues. FEBS Letters 1992; 309: 193–198
   PubMed Web of Science ®Google Scholar
• Park E. M., Shgenaga 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-xoguanine and its nucleoside derivatives from biological fluids with a monoclonal antibody column. Proceedings of the National Academy of Sciences, USA 1992; 89: 3375–3379
   PubMed Web of Science ®Google Scholar
• Prevost V., Shuker D. E. G., Bartsch H., Pastorelli R., Stillwell W. G., Trudel L. J., Tannenbaum S. R. The determination of urinary 3 methyladenine by immunoaffinity chromatography-monoclonal antibody-based ELISA: use in biomonitoring studies. Carcinogenesis 1990; 11: 1747–1751
   PubMed Web of Science ®Google Scholar
• Shigenaga M. K., Gimeno C. J., Ames B. N. Urinary 8-hydroxy-2′-deoxyguanosine as a biological marker of in vivo oxidatwe DNA damage. Proceedings of the National Academy of Sciences, USA 1989; 86: 9697–9701
   PubMed Web of Science ®Google Scholar
• Shirnamé-Morè L., Rossman T. G., Troll W., Teebor G. W., Fre Mel K. Genetic effects of 5hydroxymethyl-2′deoxyuridine, a product of ionizing radiation. Mutation Research 1987; 178: 177–186
   PubMed Web of Science ®Google Scholar
• Simic M. G., Bergtold O. S. Dietary modulation of DNA damage in humans. Mutation Research 1991; 250: 17–24
   PubMed Web of Science ®Google Scholar
• Snedecor G. W., Cochran W. G. Statistical Methods. Iowa State University Press, Ames, Iowa 1987
   Google Scholar
• Surunr J., Inoue Y., Suzuki S. Changes in the urinary excretion level of 8-ydroxyguanine by exposure to reactive oxygen-generating substances. Free Radical Biology Medicine 1995; 18: 431–436
   PubMed Web of Science ®Google Scholar
• Tèou R., Cadet J. Radiationinduced degradation of the base component in DNA and related substances. Final products. In Molecular Biology, Biochemistry and Biophysics. Effects of Ionizing Radiation on DNA Physical, Chemical and Biological Aspects, J. Hüttermann, W. Köhnlein, R. Téoule, A. J. Bertinchamps. Springer-Verlag, Berlin, Heidelberg, New York 1978; Vol. 27.: 171–203
   Google Scholar
• van Poppel G., Pousen H. E., Loft S., Verhagen H. No influence of beta carotene on oxidative DNA damage in male smokers. Journal of the National Cancer Institute 1995; 87: 310–311
   PubMedGoogle Scholar
• Verhagen H., Poulsen H. E., Loft S., van Poppel G., Wilems M. I., van Bladeren P. J. Reduction of oxidative DNA-damage in humans by Brussel sprouts. Carcinogenesis 1995; 16: 969–970
   PubMed Web of Science ®Google Scholar
• Waschke S., Reefschlager J., Barwolff D., Langen P. 5-Hydroxymethyl-2′deoxyuridine, a normal DNA constituent in certainBacillus subtilis phages is cytostatic for mammalian cells. Nature 1975; 255: 629–630
   PubMed Web of Science ®Google Scholar
• White I. R., Brunner E. J., Barron J. L. A comparison of overnight and 24 hour collection to measure urinary catecholamines. Journal of Clinical Epidemiology 1995; 48: 263–267
   PubMed Web of Science ®Google Scholar