References
- Wagner J. R., Hu C.-C., Ames B. N. Endogenous oxidative damage of deoxycytidine in DNA. Proceedings of the National Academy of Sciences USA 1992; 89: 3380–3384
- Schacter E., Beecham E. J., McCovey J. M., Kohn K. W., Potter M. Activated neutrophils induce prolonged DNA damage in neighboring cells. Carcinogenesis 1988; 9: 2297–2304
- Halliwell B., Aruoma O. I. DNA damage by oxygen-derived species. Its mechanism and measurement in mammalian systems. FEBS Letters 1991; 281: 9–19
- Weitzman S. A., Gordon L. I. Inflammation and cancer: role of phagocyte-generated oxidants in carcinogenesis. Blood 1990; 76: 655–663
- Ames B. Oxygen radicals and 8-hydroxyguanine in DNA. Japanese Journal of Cancer Research 1991; 82: 1460–1461
- 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
- Cathcart R., Schwiers 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: 5633–5637
- Richter C., Park J. W., Ames B. N. Normal oxidative damage to mitochondrial and nuclear DNA is extensive. Proceedings of the National Academy of Sciences USA 1988; 85: 6465–6467
- Adelman R., Saul R. L., Ames B. N. Oxidative damage to DNA: relation to species metabolic rate and life span. Proceedings of the National Academy of Sciences USA 1988; 85: 2706–2708
- Halliwell B., Gutteridge J. M.C. Free Radicals in Biology and Medicine, 2nd Edition. Clarendon Press, Oxford 1989
- Cutler R. G. Antioxidants and aging. American Journal of Clinical Nutrition 1991; 53: 373S–379S
- Ames B. N. Dietary carcinogens and anticarcinogens. Science 1983; 221: 1256–1264
- Ames B. N. Endogenous oxidative DNA damage, aging, and cancer. Free Radical Research Communications 1989; 7: 121–128
- Floyd R. A., Watson J. J., Harris J., West M., Wong P. K. Formation of 8-hydroxydeoxyguanosine, hydroxyl free radical adduct of DNA in granulocytes exposed to the tumor promoter, tetradeconylphorbolacetate. Biochemical and Biophysical Research Communications 1986; 137: 841–846
- Kasai H., Okada Y., Nishimura S., Rao M. S., Reddy J. K. Formation of 8-hydroxydeoxyguanosine in liver DNA of rats following long-term exposure to a peroxisome prolifer-ator. Cancer Research 1989; 49: 2603–2605
- 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 Sciences USA 1990; 87: 4533–4537
- Roy D., Floyd R. A., Liehr J. G. Elevated 8-hydroxydeoxyguanosine levels in DNA of diethylstilbestrol-treated Syrian hamsters: Covalent DNA damage by free radicals generated by redox cycling of diethylstilbestrol. Cancer Research 1991; 51: 3882–3885
- Weitzman S. A., Turk P. W., Milkowski D. H., Kozlowski K. Free radical adducts induce alterations in DNA cytosine methylation. Proceedings of the National Academy of Sciences USA 1994; 91: 1261–1264
- Malins D. C., Haimonot R. Major alterations in the nucleotide structure of DNA in cancer of the female breast. Cancer Research 1991; 51: 5430–5432
- Pryor W. A. Why is the hydroxyl radical the only radical that commonly adds to DNA? Hypothesis: it has a rare combination of high electrophilicity, high thermochemical reactivity, and a mode of production that can occur near DNA. Free Radical Biology and Medicine 1988; 4: 219–223
- Wood M. L., Dizdaroglu M., Gajewski E., Essigmann J. M. Mechanistic studies of ionizing radiation and oxidative mutagenesis: genetic effects of a single 8-hydroxyguanine (7-hydro-8-oxoguan-ine) residue inserted at a unique site in a viral genome. Biochemistry 1990; 29: 7024–7032
- Jones D. S., Nemoto F., Kuchino Y., Ohtsuka E., Nishimura S. 8-Hydroxydeoxyguanosine in DNA inhibits restriction endonuclease digestion. Nucleosides and Nucleotides 1990; 9: 223–233
- Moriya M., Ou C., Bodepudi V., Johnson F., Takeshita M., Grollman A. P. Site-specific mutagenesis using a gapped duplex vector: a study of translesion synthesis past 8-oxodeoxygaunosine in E. coli. Mutation Research 1991; 254: 281–288
- McClelland M., Nelson M., Raschke E. Effect of site-specific modification on restriction endonucleases and DNA modification methyltransferases. Nucleic Acids Research 1994; 22: 3640–3659