8-Hydroxydeoxyguanosine in DNA from TPA-Stimulated Human Granulocytes

References

• Floyd R. A., Watson J. J., Wong P. K., Altmiller D. H., Richard R. C. Hydroxyl free radical adduct of deoxyguanosine: sensitive detection and mechanisms of formation. Free Radical Research Communications 1986; 1: 163–172
   PubMedGoogle Scholar
• Floyd R. A. Role of oxygen free radicals in carcinogenesis and brain ischemia. FASEB Journal 1990; 4: 2587–2597
   PubMed Web of Science ®Google Scholar
• Park J.-W., Floyd R. A. Lipid peroxidation products mediate the formation of 8-hydroxydeoxyguanosine in DNA. Free Radical Biology & Medicine 1992; 12: 245–250
   PubMed Web of Science ®Google Scholar
• Floyd R. A., West M. S., Eneff K. L., Hogsett W. E., Tingey D. T. Hydroxyl free radical mediated formation of 8-hydroxyguanine in isolated DNA. Archives of Biochemistry and Biophysics 1988; 262: 266–272
   PubMed Web of Science ®Google Scholar
• Devasagayam T. P.A., Steenken S., Obendorf M. S.W., Schulz W. A., Sies H. Formation of 8-hydroxy(deoxy)guanosine and generation of strand breaks at guanine residues in DNA be singlet oxygen. Biochemistry 1991; 30: 6283–6289
   PubMed Web of Science ®Google Scholar
• Kaur H., Fagerheim I., Grootveld M., Puppo A., Halliwell B. Aromatic hydroxylation of phenylalanine as an assay for hydroxyl radicals: application to activated human neutrophils and to the heme protein leghemoglobin. Analytical Biochemistry 1988; 172: 360–367
   PubMed Web of Science ®Google Scholar
• Samuni A., Black C. D.V., Krishna C. M., Malech H. L., Berstein E. F., Russo A. Hydroxyl radical production by stimulated neutrophils reappraised. Journal of Biological Chemistry 1988; 263: 13797–13801
   PubMed Web of Science ®Google Scholar
• Britigan B. E., Hassett D. J., Rosen G. M., Hamill D. R., Cohen M. S. Neutrophil degranulation inhibits potential hydroxyl-radical formation. Relative impact of myeloperoxidase and lacto-ferrin release on hydroxyl-radical production by iron-supplemented neutrophils assessed by spin-trapping techniques. Biochemical Journal 1989; 264: 447–455
   PubMedGoogle Scholar
• Pou S., Rosen G. M., Britigan B. E., Cohen M. S. Intracellular spin-trapping of oxygen-centered radicals generated by human neutrophils. Biochimica Biophysica Acta 1989; 991: 459–464
   PubMedGoogle Scholar
• Greenwald R. A., Rush S. W., Moak S. A., Weitz Z. Conversion of superoxide generated by polymorphonuclear leukocytes to hydroxyl radical: A direct spectrophotometric detection system based on degradation of deoxyribose. Free Radical Biology & Medicine 1989; 6: 385–392
   PubMedGoogle Scholar
• Britigan B. E., Coffman T. J., Buettner G. R. Spin trapping evidence for the lack of significant hydroxyl radical production during the respiration burst of human phagocytes using a spin adduct resistant to superoxide-mediated destruction. Journal of Biological Chemistry 1990; 265: 2650–2656
   PubMed Web of Science ®Google Scholar
• Britigan B. E., Edeker B. L. Pseudomonas and neutrophil products modify transferrin and lactoferrin to create conditions that favor hydroxyl radical formation. Journal of Clinical Investigation 1991; 88: 1092–1102
   PubMed Web of Science ®Google Scholar
• Floyd R. A., Watson J. J., Harris J., West M., Wong P. K. Formation of 8-hydroxydeoxy-guanosine, hydroxyl free radical adduct of DNA in granulocytes exposed to the tumor promoter, tetradecanoylphorbolacetate. Biochemical and Biophysical Research Communications 1986; 137: 841–846
   PubMed Web of Science ®Google Scholar
• Birnboim H. C. DNA strand breakage in human leukocytes exposed to a tumor promoter, phorbol myristate acetate. Science 1982; 215: 1247–1249
   PubMed Web of Science ®Google Scholar
• Birnboim H. C., Kanabus-Kaminska M. The production of DNA strand breaks in human leukocytes by superoxide anion may involve a metabolic process. Proceedings of the National Academy of Science U.S.A. 1985; 82: 6820–6824
   PubMed Web of Science ®Google Scholar
• Birnboim H. C. Superoxide anion may trigger DNA strand breaks in human granulocytes by acting at a membrane target In Annals of the New York Academy of Sciences. Membrane in Cancer Cells, T. Galeotti, A. Cittadini, G. Neri, A. Scarpa. The New York Academy of Sciences, New York 1988; 551: 83–94
   Google Scholar
• Birnboim H. C. Effect of lipophilic chelators on oxyradical-induced DNA strand breaks in human granulocytes: Paradoxical effect of 1,10-phenantnroline. Archives of Biochemistry and Biophysics 1992; 294: 17–21
   PubMedGoogle Scholar
• Birnboim H. C. A superoxide anion-induced DNA strand break metabolic pathway in human leukocytes: Effects of vanadate. Biochemistry and Cell Biology 1988; 66: 374–381
   PubMedGoogle Scholar
• Birnboim H. C. Fluorometric analysis of DNA unwinding to study strand breaks and repair in mammalian cells. Methods in Enzymology 1990; 186: 550–555
   PubMedGoogle Scholar
• Birnboim H. C. Extraction of high molecular weight RNA and DNA from cultured mammalian cells. Methods in Enzymology 1993; 216: 154–160
   Google Scholar
• Birnboim H. C. Rapid extraction of high molecular weight RNA from cultured cells for Northern analysis. Nucleic Acids Research 1988; 16: 1487–1497
   PubMed Web of Science ®Google Scholar
• Floyd R. A., West M. S., Eneff K. L., et al. Conditions influencing yield and analysis of 8-hydroxy-2′-deoxyguanosine in oxidatively damaged DNA. Analytical Biochemistry 1990; 188: 155–158
   PubMed Web of Science ®Google Scholar
• McWilliams R. S., Cross W. G., Kaplan J. G., Birnboim H. C. Rapid rejoining of DNA strand breaks in resting human lymphocytes after irradiation by low doses of 60CO τ rays or 14.6-MeV neutrons. Radiation Research 1983; 94: 499–507
   PubMed Web of Science ®Google Scholar
• Aruoma O. I., Halliwell B., Gajewski E., Dizdaroglu M. Copper-ion-dependent damage to the bases in DNA in the presence of hydrogen peroxide. Biochemical Journal 1991; 273: 601–604
   PubMed Web of Science ®Google Scholar
• Dizdaroglu M., Olinski R., Doroshow J. H., Akman S. A. Modification of DNA bases in chromatin of intact target human cells by activated human polymorphonuclear leukocytes. Cancer Research 1993; 53: 1269–1272
   PubMed Web of Science ®Google Scholar
• Schraufstatter I., Hyslop P. A., Jackson J. H., Cochrane C. G. Oxidant-induced DNA damage of target cells. Journal of Clinical Investigation 1988; 82: 1040–1050
   PubMed Web of Science ®Google Scholar
• Lindahl T. Instability and decay of the primary structure of DNA. Nature 1993; 362: 709–715
   PubMed Web of Science ®Google Scholar
• Olinski 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
• Fraga C. G., Shigenaga M. K., Park J. W., Degan P., Ames B. N. Oxidative damage to DNA during aging: 8-hydroxy-2′-deoxyguanosine in rat organ DNA and urine. Proceedings of the National Academy of Science U.S.A. 1990; 87: 4533–4537
   PubMed Web of Science ®Google Scholar
• Fiala E. M., Conaway C. C., Mathis J. E. Oxidative DNA and RNA damage in the livers of Sprague-Dawley rats treated with the hepatocarcinogen, 2-nitropropane. Cancer Research 1989; 49: 5518–5522
   PubMed Web of Science ®Google Scholar
• Kasai H., Crain P. F., Kuchino Y., Nishimura S., Ootsuyama A., Tanooka H. Formation of 8-hydroxyguanine moiety in cellular DNA by agents producing oxygen radicals and evidence for its repair. Carcinogenesis 1986; 7: 1849–1851
   PubMed Web of Science ®Google Scholar
• Claycamp H. G. Phenol sensitization of DNA to subsequent oxidative damage in 8-hydroxyguanine assays. Carcinogenesis 1992; 13: 1289–1292
   PubMed Web of Science ®Google Scholar
• Myers D. K. Low level radiation: a review of current estimates of hazards to human populations. Atomic Energy of Canada Limited, Chalk River, Ontario 1977, Publication No. 5715
   Google Scholar