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Original Article

Methodological considerations and factors affecting 8-hydroxy-2′-deoxyguanosine analysis

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Pages 511-524 | Received 14 Jul 1998, Published online: 07 Jul 2009

References

  • Fraga C.G., Shingenaga 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 in the United States of America 1990; 87: 4690–4537
  • Tchou T., Kasai H., Shibutatni S., Chung M.H., Laval J., Grollman A.P., Nishimura S. 8-Oxoguanine (8-hydroxy-guanine) DNA glycosilase and its substrate specificity. Proceedings of the National Academy of Sciences in the United States of America 1991; 88: 4690–4694
  • Tchou J., Michaels M.L., Miller J.H., Grollman A.P. Function of the zincn finger in Escherichia coli Fpg protein. Journal of Biological Chemistry 1993; 268: 26738–26744
  • Lee Y.S., Lee H.S., Park M.K., Hwang E.S., Park E.M., Kasai H., Chung M.H. Identification of 8-hydroxyguanine glycosylase activity in mammalian tissues using 8-hydroxyguanine specific monoclonal antibody. Biochemical & Biophysical Research Communications 1993; 196: 1545–1551
  • Sakumi K., Furuichi M., Tsuzuki T., Kakuma T., Kawabata S., Maki H., Sekiguchi M. Cloning and expression of cDNA synthesis. Journal of Biological Chemistry 1993; 268: 23524–23530
  • Lindahl T. Instability and decay of the primary structure of DNA. Nature 1993; 362: 709–715
  • Floyd R.A. The role of 8-hydroxyguanine in carcinogenesis. Carcinogenesis 1990; 11: 1447–1450
  • Hayakawa M., Torii K., Sugiyama S., Tanaka M., Ozawa T. Age associated accumulation of 8-hydroxyguanosine in mitochondrial DNA of human diaphragm. Biochemical & Biophysical Research Communications 1991; 179: 1023–1029
  • Clayson D.B., Mhta R., Iverson F. International commission for protection against environmental mutagens and carcinogens. Oxidative DNA damage — the effects of certain genotoxic and operationally nongenotoxic carcinogens. Mutation Research 1994; 317: 25–42
  • Shimoda R., Nagashima M., Sakamoto M., Yamaguchi N., Hirohashi S., Yokota J., Kasai H. Increased formation of oxidative DNA damage, 8-hydroxydeoxy-guanosine, in human livers with chronic hepatitis. Cancer Research 1994; 54: 3171–3172
  • Loft S., Astrup A., Buemann B., Poulsen H.E. Oxidative damage correlates with oxygen consumption in humans. FASEB Journal 1994; 8: 534–537
  • Povey A.C., Wilson V.L., Weston A., Doan V.T., Wood M.L., Essigmann J.M., Shields P.G. Detection of oxidative damage by 32P-postlabelling: 8-hydroxydeoxy-guanosine as a marker of exposure. Postlabelling Methods for Detection of DNA Adducts, Phillips, Castegnaro, Bartsch. IARC, LyonFrance 1993; 105–114, In
  • Dandona P., Thusu K., Snyder B., Makowski J., Armstrong D., Nicotera T. Oxidative damage to DNA in diabetes mellitus. The Lancet 1996; 347: 444–445
  • Kitahara M., Eyre H.J., Lynch R.E., Rallison M.L., Hill H.R. Metabolic activity of diabetics monocytes. Diabetes 1980; 29: 251–256
  • Armstrong D., Al-Awadi F. Lipid peroxidation and retinopathy in steptozotocin induced diabetes. Free Radical Biology & Medicine 1991; 11: 433–436
  • Britton R.S., Bacon B.R. Role of free radicals in liver diseases and hepatic fibrosis. Hepato-Gastroenterology 1994; 41: 342–348
  • Bjorneboe A., Bjorneboe G.E. Antioxidant status and alcohol related diseases. Alkohol & Alkoholism 1993; 28: 111–116
  • Stewart M.S., Cameron G.S., Pence B.C. Antioxidant nutrients protect against UVB-induced oxidative damage to DNA of mouse keratinocytes in culture. Journal of Investigative Dermatology 1996; 106: 1086–1089
  • Hattori Y., Nishigori C., Tanaka T., Uchida K., Nikaido O., Osawa T., Hiai H., Imamura S., Toyokuni S. 8-hydroxy-2′-deoxyguanosine is increased in epidermal cells of hairless mice after chronic ultraviolet B exposure. Journal of Investigative Dermatology 1997; 107: 733–737
  • Wei H., Cai Q., Rahn R., Zhang X. Singlet oxygen involvement in (254nm) radiation-induced formation of 8-hydroxy-deoxyguanosine in DNA. Free Radical Biology & Medicine 1997; 23: 148–154
  • Xueliang H., Liehr J. 8-hydroxylation of guanine bases in kidney and liver DNA of hamsters treated with estradiol: role of free radicals in estrogen-induced carcinogenesis. Cancer Research 1994; 54: 5515–5517
  • Sai K., Umemura T., Takagi A., Hasegawa R., Kurokawa Y. The protective role of glutathione, cysteine and vitamin C against oxidative DNA damage induced in rat kidney by potassium bromate. Japanese Journal of Cancer Research 1992; 83: 45–51
  • Takeuchi T., Nakajima M., Morimoto K. Establishment of a human system that generates O2 and induces 8-hydroxyguanosins, typical of oxidative DNA damage, by a tumor promotor. Cancer Research 1994; 54: 5837–5840
  • Halliwell B., Gutteridge J.M.C. Free Radicals in Biology and Medicine. Clarendon Press, Oxford 1989
  • Hofer T., Möller L. Reduction of oxidation during the preparation of DNA and analysis of 8-hydroxy-2′-deoxyguanosine. Chemical Research in Toxicology 1998, in press
  • Vincent J.B., Crowder M.W., Averill B.A. Hydrolysis of phosphate monoesters: a biological problem with multiple chemical solutions. TIBS 1992; 17: 105–110
  • Chemikov A.V., Usacheva A.M., Bruskov V.I. Depurination of 8-oxo-7,8-dihydroguanine (8-hydroxyguanine) nucleosides. Biochemistry (Moscow) 1996; 61: 35–38
  • Jenner A., England T.G., Aruoma O.I., Halliwell B. Measurement of oxidative DNA damage by gas chromatography-mass spectrometry: ethanethiol prevents artifactual generation of oxidized DNA bases. Biochemical Journal 1998; 331: 365–369
  • Serrano J., Palmeira C.M., Wallace K.B., Kuehl D.W. Determination of 8-hydroxydeoxyguanosine in biological tissue by liquid chromatography/electrospray ionization-mass spectrometry/mass spectrometry. Rapid Communications in Mass Spectrometry 1996; 10: 1789–1791
  • Breen A.P., Murphy J.A. Reactions of oxyl radicals with DNA. Free Radical Biology & Medicine 1995; 18: 1033–1077
  • Möller L., Hofer T. [32P]ATP mediates formation of 8-hydroxy-2′-deoxyguanosine from 2′-deoxyguanosine, a possible problem in the 32P-postlabeling assay. Carcinogenesis 1997; 18: 2415–2419
  • Tagaki A., Sai K., Umemura T., Hasegawa R., Kurokawa Y. Inhibitory effects of vitamin E and ellagic acid on 8-hydroxy-deoxyguanosine formation in liver nuclear DNA of rats treated with 2-nitropropane. Cancer Letters 1995; 91: 139–144
  • Nakae D., Mizumoto Y., Kobayashi E., Noguchi O., Konishi Y. Improved genomic/nuclear DNA extraction for 8-hydroxydeoxyguanosine analysis of small amounts of rat liver tissue. Cancer Letters 1995; 97: 233–239
  • Beckman K.B., Ames B.N. Detection and quantification of oxidative adducts of mitochondrial DNA. Methods in Enzymology 1996; 264: 442–453
  • 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-oxo-guanine. Proceedings of the National Academy of Sciences in the United States of America 1998; 95: 288–293
  • Samuni A., Krishna M.C. Antioxidant properties of nitroxides and nitroxide SOD mimics. Handbook of Synthetic Antioxidants, L. Packer, E. Cedenas. M. Dekker, New York 1997; 351–373, In
  • Buettner G.R., Jurkiewicz B.A. Ascorbate radical: a valuable marker of oxidative stress. Analysis of Free Radicals in Biological Systems, A.E. Favier, J. Cadet, B. Kalyanaraman, M. Fontecave, J.-L. Pierre. Birkhäuser Verlag, Basel 1995; 145–164, In
  • Halliwell B. Vitamin C: antioxidant or pro-oxidant in vitro?. Free Radical Research 1996; 25: 439–454
  • Park J.-W., Floyd R.A. Glutathione/Fe3+/O2-mediated DNA strand breaks and 8-hydroxydeoxyguanosine formation. Biochimica et Biophysica Acta 1997; 1336: 263–268
  • Park J.-W., Floyd R.A. Generation of strand breaks and formation of 8-hydroxy-2′deoxyguanosine in DNA by a thiol/Fe3+/O2-catalyzed oxidation system. Archives of Biochemistry and Biophysics 1994; 312: 285–291
  • Spear N., Aust S.D. The effects of different buffers on the oxidation of DNA by thiols and ferric iron. Journal of Biochemistry and Molecular Toxicology 1998; 12: 125–132
  • Lardinois O.M., Mestdagh M.M., Rouxhet P.G. Reversible inhibition and irreversible inactivation of catalase in presence of hydrogen peroxide. Biochimica and Biophysica Acta 1996; 1295: 222–238
  • Barton D.H.R., Choi S.-Y., Hu B., Smith J.A. Evidence for a higher oxidation state of manganese in the reaction of dinuclear manganese complexes with oxidants. Comparison with iron based gif chemistry. Tetrahedron 1998; 54: 3367–3378
  • Aruoma O.I., Halliwell B., Dizdaroglu M. Iron ion-dependent modification of bases in DNA by the superoxide radical-generating system hypoxanthine/xanthine oxidase. The Journal of Biological Chemistry 1989; 264: 13024–13028
  • Galey J.-B. Potential use of iron chelators against oxidative damage. Antioxidants in Disease Mechanisms and Therapy, H. Sies. Academic Press, London and New York 1997; 167–203, In
  • Burkitt M.J., Milne L., Nicotera P., Orrenius S. 1,10-Phenanthroline stimulates internucleosomal DNA fragmentation in isolated rat-liver nuclei by promoting the redox activity of endogenous copper ions. Biochemical Journal 1996; 313: 163–169
  • Young H.K., Floyd R.A., Maidt M.L., Dynlacht J.R. Evaluation of nitrone spin-trapping agents as radioprotectors. Radiation Research 1996; 146: 227–231
  • Randerath K., Reddy M.V., Gupta R.C. 32P-Labelling test for DNA damage. Proceedings of the National Academy of Sciences of the United States of America 1981; 78: 6126–6129
  • Gupta R.C., Reddy M.V., Randerath K. 32P-Postlabelling analysis of nonradioactive aromatic carcinogen-DNA adducts. Carcinogenesis 1982; 3: 1081–1092
  • Gupta R.C. Enhanced sensitivity of 32P-postlabelling analysis of aromatic carcinogen:DNA adducts. Cancer Research 1985; 45: 5656–5662
  • Reddy M.V., Randerath K. Nuclease P1-mediated enhancement of sensitivity of 32P-postlabelling test for structurally diverse DNA adducts. Carcinogenesis 1986; 7: 1543–1551
  • Beach A.C., Gupta R.C. Human biomonitoring and the 32P-postlabeling assay. Carcinogenesis 1992; 13: 1053–1074
  • Levy G.N., Weber W.W. High-performance liquid chromatographic analysis of 32P-postlabeled DNA-aromatic carcinogen adducts. Analytical Biochemistry 1988; 174: 381–392
  • Weyand E.H., Rice J.E., LaVoie E.J. 32P-postlabeling analysis of DNA adducts from non-alternant PAH using thin-layer and high performance liquid chromatography. Cancer Letters 1987; 37: 257–266
  • Möller L., Zeisig M. DNA adduct formation after oral administration of 2-nitrofluorene and N-acetyl-2-aminofluorene, analyzed by 32P-TLC and 32P-HPLC. Carcinogenesis 1993; 14: 53–59
  • Möller L., Zeisig M., Vodicka P. Optimization of an HPLC method for analyses of 32P-postlabeled DNA adducts. Carcinogenesis 1993; 14: 1343–1348
  • Zeisig M., Möller L. 32P-Postlabeling high-performance liquid chromatographic improvements to characterize DNA adduct stereoisomers from benzo[]pyrene and benzo[c]phenanthrene, and to separate DNA adducts from 7,12-dimethylbenz[]anthracene. Journal of Chromatography B Biomedical Applications 1997; 691: 341–350
  • Zeisig M., Möller L. Accelerated paper: 32P-HPLC suitable for characterization of DNA adducts formed in vitro by polycyclic aromatic hydrocarbons and derivatives. Carcinogenesis 1995; 16: 1–9
  • Möller L., Grzybowska E., Zeisig M., Cimander B., Hemminki K., Chorazy M. Seasonal variations of DNA adduct pattern in human lymphocytes analyzed by 32P-HPLC. Carcinogenesis 1995; 17: 61–66
  • Möller L., Cui X.-S., Torndal U.-B., Ericsson L.C. Preneoplastic lesions and DNA adduct formation of the airborne genotoxic agents 2-nitrofluorene and 2,7-dinitrofluorene. Carcinogenesis 1993; 14: 2627–2632
  • Möller L., Zeisig M., Midtvedt T., Gustafsson J.A. Intestinal microflora enhances formation of DNA adducts following administration of 2-NF and 2-AAF. Carcinogenesis 1994; 15: 857–861
  • Wohlin P., Zeisig M., Gustafsson J.-A., Möller L. 32P HPLC analysis of DNA adducts formed in vitro and in vivo by 2-amino-1-methyl-6-phenylimidazo [4,5-b]pyridine and 2-amino-3,4,8-trimethyl-3H-imidazo [4,5-f]quinoxaline, utilizing an improved adduct enrichment procedure. Chemical Research in Toxicology 1996; 9: 1050–1056
  • Zeisig M., Cadet J., Möller L. 32P-Postlabeling high-performance liquid chromatography (32P-HPLC) adapted for analysis of 8-hydroxy-2′-deoxyguanosine (submitted). 1998
  • Lutgerink J.T., de Graaf E., Hoebee B., Stavenuitez H.F.C., Westra J.G., Kriek E. Detection of 8-hydroxyguanine in small amounts of DNA by 32P postlabeling. Analytical Biochemistry 1992; 201: 127–133
  • Devanaboyma U.-S., Gupta R.C. Sensitive detection of 8-hydroxy-2′-deoxyguanosine in DNA by 32P-postlabeling assay and the basal levels in rat tissues. Carcinogenesis 1996; 17: 917–924
  • Schuler D., Otteneder M., Sagelsdorff P., Eder E., Gupta R.C., Lutz K. Comparative analysis of 8-oxo-2′-deoxyguanosine in DNA by 32P- and 33P-postlabeling and electrochemical detection. Carcinogenesis 1997; 18: 2367–2371
  • Wilson V.L., Taffe B.G., Shields P.G., Povey A.C., Harris C.C. Detection and quantification of 8-hydroxydeoxyguanosine adducts in peripheral blood of people exposed to ionizing radiation. Environmental Health Perspectives 1993; 99: 261–263
  • Podmore K., Farmer P.B., Herbert K.E., Jones G.D.D., Martin E.A. 32P-Postlabelling approaches for the detection of 8-oxo-2′-deoxyguanosine-3′-monophosphate in DNA. Mutation Research 1997; 178: 139–149
  • Adachi S., Zeisig M., Möller L. Improvements in the analytical method for 8-hydroxydeoxyguanosine in nuclear DNA. Carcinogenesis 1995; 16: 253–258
  • Tesfamariam B. Free radicals in diabetic endothelial cell dysfunction. Free Radical Biology and Medicine 1994; 16: 383–391
  • Hayakawa M., Kuzuya F. Free radicals and diabetes mellitus. Nippon Ronen Igakkai Zasshi 1990; 27: 149–154
  • Wolff S.P., Jiang Z.Y., Hunt J.V. Protein glycation and oxidative stress in diabetes mellitus and ageing. Free Radical Biology and Medicine 1991; 10: 339–352
  • Mecocci P., MacGarvey U., Kaufman A.E., Koonz D., Shoffner J.M., Wallace D.C., Beal M.F. Oxidative damage to mitochondrial DNA shows marked agedependent increases in human brain. Annals of Neurology 1993; 34: 609–616
  • Crary E.J., McCarty M.F. Potential clinical applications for high-dose nutritional antioxidants. Medical Hypotheses 1984; 13: 77–98
  • Kilgore K.S., Lucchesi B.R. Reperfusion injury after myocardial infarction: the role of free radicals and the inflammatory process. Clinical Biochemistry 1993; 26: 359–370
  • Baik S.-H., Youn H.-S., Chung M.-H., Lee W.-K., Cho M.-J., Ko G.-H., Park C.-K., Kasai H., Rhee K.-H. Increased oxidative DNA damage in Heliobacter pyloriinfected human gastric mucosa. Cancer Research 1996; 56: 1279–1282
  • Winrow V.R., Winyard P.G., Morris C.J., Blake D.R. Free radicals in inflammation: second messengers and mediators of tissue destruction. British Medical Bulletin 1993; 49: 506–522
  • Peretz A.M., Neve J.D., Famaey J.P. Selenium in rheumatic diseases. Seminars in Arthritis & Rheumatism 1991; 20: 305–316
  • Hatch G.E. Asthma, inhaled oxidants and dietary antioxidants. American Journal of Clinical Nutrition 1995; 61(3 Suppl)625–630
  • Degan P., Bonassi S., De Caterina M., Korkina L.G., Pinto L., Scopacasa F., Zatterale A., Calzone R., Pagano G. In vivo accumulation of 8-hydroxy-2′-deoxyguanosine in DNA correlates with release of reactive oxygen species in Fanconi's anaemia families. Carcinogenesis 1995; 16: 735–742
  • Ohshima H., Bartsch H. Chronic infections and inflammatory processes as cancer risk factors: possible role of nitric oxide in carcinogenesis. Mutation Research 1994; 305: 253–264
  • Malins D.C., Haimanot R. Major alterations in the nucleotide structure of DNA in cancer of the female breast. Cancer Research 1991; 51: 5430–5432
  • Musarrat J., Arezina-Wilson J., Wani A.A. Prognostic and aetiological relevance of 8-hydroxyguanosine in human breast carcinogenesis. European Journal of Cancer 1997; 32A: 1209–1214
  • Lih-Brody L., Powell S.R., Collier K.P., Reddy G.M., Cerchia R., Kahn E., Weissman G.S., Katz S., Floyd R.A., McKinley M.J., Fisher S.E., Mullin G.E. Increased oxidative stress and decreased antioxidant defense in mucosa of inflammatory bowel disease. Digestive Diseases and Sciences 1996; 41: 2078–2086
  • Dargel R. Lipid peroxidation — a common pathogenic mechanism?. Experimental & Toxicologic Pathology 1992; 44: 169–181
  • Bankson D.D., Kestin M., Rifai N. Role of free radicals in cancer and atherosclerosis. Clinics in Laboratory Medicine 1993; 13: 463–480
  • Liu P.K., Hsu C.Y., Dizdaroglu M., Floyd R.A., Kow Y.W., Karakaya A., Rabow L.E., Cui J.-K. Damage, repair and mutagenesis in nuclear genes after mouse forebrain ischemia-reperfusion. The Journal of Neuroscience 1996; 16: 6795–6806
  • Möller, L., et al. Karolinska Institutet, unpublished results. 1990
  • Nakano M. Free radicals and their biological significance. Human Cell 1992; 5: 334–340
  • Brown R.K., McBurney A., Lunce J., Kelly F.J. Oxidative damage to DNA in patients with cystic fibrosis. Free Radical Biology & Medicine 1995; 18: 801–806
  • Bendich A. Physiological role of antioxidants in the immune system. Journal of Dairy Science 1993; 76: 2789–2794
  • Mecocci P., MacGarvey U., Beal M.F. Oxidative damage to mitochondrial DNA is increased in Alzheimer's disease. Annals of Neurology 1994; 36: 747–751
  • Youdim M.B., Lavie L. Selective MAO-A and B inhibitors, radical scavengers and nitric oxide synthase inhibitors in Parkinson's disease. Life Sciences 1994; 55: 2077–2082
  • Ward J. Free radicals, antioxidants and preventive geriatrics. Australian Family Physician 1994; 23: 1297–1301
  • Pincemail J. Free radicals and antioxidants in human diseases. Analysis of Free Radicals in Biological Systems, A.E. Favier, J. Cadet, B. Kalyanaraman, M. Fontecave, J.-L. Pierre, 1995, In
  • Adachi S., Kawamura K., Yoshida S., Takemoto K. Oxidative damage on DNA induced by asbestos and man-made fibers in vitro. International Archives of Occupational and Environal Health 1992; 63: 553–557
  • Plummer S.M., Faux S.P. Induction of 8-hydroxy-deoxyguanosine in isolated DNA and HeLa cells exposed to fecapentaene-12: evidence for the involvement of prostaglandin H synthase and iron. Carcinogenesis 1994; 15: 449–453
  • Shi X., Sun X., Gannett P.M., Dalal N.S. Deferoxamine inhibition of Cr(V)-mediated radical generation and deoxyguanine hydroxylation: ESR and HPLC evidence. Archives of Biochemistry and Biophysics 1992; 293: 281–286
  • Shi X., Jiang H., Mao Y., Ye J., Saffiotti U. Vanadium(IV)-mediated free radical generation and related 2′-deoxyguanosine hydroxylation and DNA damage. Toxicology 1996; 106: 27–38
  • Mikhailova M.V., Littlefield N.A., Hass B.S., Poirier L.A., Chou M.W. Cadmium-induced 8-hydroxy-deoxyguanosine formation, DNA strand breaks and antioxidant enzyme activities in lymphoblastoid cells. Cancer Letters 1997; 115: 141–148
  • Shen H.M., Ong C.N., Lee B.L., Shi C.Y. Aflatoxin B1-induced 8-hydroxydeoxyguanosine formation in rat hepatic DNA. Carcinogenesis 1995; 16: 419–422
  • Austin E.W., Parrish J.M., Kinder D.H., Bull R.J. Lipid peroxidation and formation of 8-hydroxy-deoxyguanosine from acute doses of halogenated acetic acids. Fundamental and Applied Toxicology 1996; 31: 77–82
  • Loft S., Vistisen K., Ewertz M., Tjønneland A., Overvad K., Poulsen H.E. Oxidative DNA damage estimated by 8-hydroxydeoxyguanosine excretion in humans: influence of smoking, gender and body mass index. Carcinogenesis 1992; 13: 2241–2247
  • Sai-Kato K., Umemura T., Takagi A., Hasegawa R., Tanimura A., Kurokawa Y. Pentachlorophenol-induced oxidative DNA damage in mouse liver and protective effect of antioxidants. Food & Chemical Toxicology 1995; 33: 877–882
  • Mustafa M.G. Biochemical basis of ozone toxicity. Free Radical Biology & Medicine 1990; 9: 245–265
  • Bhimani R.S., Troll W., Grunberger D., Frenkel K. Inhibition of oxidative stress in HeLa cells by chemopreventive agents. Cancer Research 1993; 53: 4528–4533
  • Sipowicz M.A., Amin S., Desai D., Kasprzak K.S., Anderson L.M. Oxidative DNA damage in tissues of pregnant female mice and fetuses caused by the tobacco-specific nitrosamine, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK). Cancer Letters 1997; 117: 87–91
  • Lagorio S., Tagesson C., Forastiere F., Iavarone I., Axelson O., Carere A. Exposure to benzene and urinary concentrations of 8-hydroxydeoxyguanosine, a biological marker of oxidative damage to DNA. Occupational and Environmental Medicine 1994; 51: 739–743
  • Liu T.-Y., Chen C.-L., Chi C.-W. Oxidative damage to DNA induced by areca nut extract. Mutation Research 1996; 367: 25–31
  • Olinski R., Zastawny T.H., Foksinski M., Windorbska W., Jaruga P., Dizdaroglu M. DNA base damage in lymphocytes of cancer patients undergoing radiation therapy. Cancer Letters 1996; 106: 207–215

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