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Urinary excretion of mutagens and covalent DNA damage induced in the bladder and kidney after passive smoking in rats

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Abstract

Using 32P-postlabeling assay, we studied the effect of sidestream smoke of cigarettes, so-called passive smoking, on the covalent DNA adduct formation in an animal model. Urine samples of 18 rats, 9 male and 9 female, before smoking resulted in an average of 2.4 adducts per 1×107 nucleotides per 24-h urine of a rat in the target plasmid DNA after incubation for 2 h in vitro. Urine samples of 4 out of 6 rats after exposure to sidestream smoke induced additional adducts in the target DNA. The incidence increased to 17.5 adducts per 1×107 nucleotides per 24-h urine of a rat. Without exposure to smoke, no increase in the adduct formation was observed. Adduct formations similar to those induced in vitro were detected in the bladder and kidney DNA, but not in the testicular DNA, of the four rats exposed to sidestream smoke. These observations suggest that passive smoking causes covalent DNA damage of the cells in the bladder and kidney by excreting chemicals in urine. Passive smoking as well as active smoking might contribute to the bladder and renal carcinogenic process.

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References

  1. Adams JD, Lee SJ, Hoffmann D (1984) Carcinogenic agents in cigarette smoke and the influence of nitrate on their formation. Carcinogenesis 5:221

    Google Scholar 

  2. Augustine A, Hebert JR, Kabat GC, Wynder EL (1988) Bladder cancer in relation to cigarette smoking. Cancer Res 48:4405

    Google Scholar 

  3. Bos RP, Theuws JLG, Henderson PT (1983) Excretion of mutagens in human urine after passive smoking. Cancer Lett 19:85

    Google Scholar 

  4. Correa P, Pickle LW, Fontham E, Lin Y, Haenszel W (1983) Passive smoking and lung cancer. Lancet 2:595

    Google Scholar 

  5. Cuzick J, Routledge MN, Jenkins D, Garner RC (1990) DNA adducts in different tissues of smokers and non-smokers. Int J Cancer 45:673

    Google Scholar 

  6. Davis LG, Dibner MD, Battey JF (eds) (1984) Preparation of DNA from eukaryotic cells. In: Basic Methods in Molecular Biology. Elsevier, New York, p 42

    Google Scholar 

  7. Druckrey H (1975) Chemical carcinogenesis of N-nitroso derivatives. In: Gann Monograph. University Park Press, Baltimore, p 107

    Google Scholar 

  8. Evans HJ, Fletcher J, Torrance M, Hargreave TB (1981) Sperm abnormalities and cigarette smoking. Lancet I:627

    Google Scholar 

  9. Everson RB, Randerath E, Santella K (1986) Detection of smoking-related covalent DNA adducts in human placenta. Science 231:54

    Google Scholar 

  10. Galuskinova V (1964) 3,4-Benzpyrene determination in the smoky atmosphere of social meeting rooms and restaurants. A contribution to the problem of the noxiousness of so-called passive smoking. Neoplasma 11:35

    Google Scholar 

  11. Gupta RC, Reddy MV, Randerath K (1982) 32P-postlabeling analysis of non-radioactive aromatic carcinogen-DNA adducts. Carcinogenesis 3:1081

    Google Scholar 

  12. Hayatsu H, Oka T, Wakata A, Ohara Y, Hayatsu T, Kobayashi H, Arimoto S (1983) Adsorption of mutagens to cotton bearing covalently bound trisulfo-copper-phthalocyanine. Mutation Res 119:233

    Google Scholar 

  13. Horowitz JM, Park SH, Bogenmann E, Cheng JC, Yandell DW, Kaye FJ, Minna JD, Dryja TP, Weinberg RA (1990) Frequent inactivation of the retinoblastoma anti-oncogene is restricted to a subset of human tumor cells. Proc Natl Acad Sci USA 87:2775

    Google Scholar 

  14. Kanaoka T, Miyakawa M, Yoshida O (1990) Study on influence of cigarette smoking on the mutagenicity of urine. II. Animal experimental model of passive smoking. Acta Urol Jpn 36:395

    Google Scholar 

  15. Kulikauskas V, Blaustein D, Ablin RJ (1985) Cigarette smoking and its possible effects on sperm. Fertil Steril 44:526

    Google Scholar 

  16. Marshall CJ, Vousden KH, Phillips DH (1984) Activation of c-Ha-ras-1 proto-oncogene by in vitro modification with a chemical carcinogen, benzo(a)pyrene diol-epoxide. Nature 310:586

    Google Scholar 

  17. McCann J, Choi E, Yamasaki E, Ames BN (1975) Detection of carcinogens as mutagens in the Salmonella/microsome test: assay of 300 chemicals. Proc Natl Acad Sci USA 72:5135

    Google Scholar 

  18. Miller EC (1978) Some current perspectives on chemical carcinogenesis in humans and experimental animals: presidential address. Cancer Res 38:1479

    Google Scholar 

  19. Mommsen S, Aagaard J (1983) Tobacco as a risk factor in bladder cancer. Carcinogenesis 4:335

    Google Scholar 

  20. Quintanilla M, Brown K, Ramsden M, Balmain A (1986) Carcinogen specific mutation and amplification of Ha-ras during mouse skin carcinogenesis. Nature 322:78

    Google Scholar 

  21. Reddy MV, Randerath K (1986) Nuclease P1-mediated enhancement of sensitivity of 32P-postlabeling test for structurally diverse DNA adducts. Carcinogenesis 7:1543

    Google Scholar 

  22. Rowland RG, Henneberry MO, Oyasu R, Grayhack JT (1980) Effects of urine and continued exposure to carcinogen on progression of early neoplastic urinary bladder lesion. Cancer Res 40:4525

    Google Scholar 

  23. Shaarawy M, Mahmoud KZ (1982) Endocrine profile and semen characteristics in male smokers. Fertil Steril 38:255

    Google Scholar 

  24. Sidransky D, Eschenbach AV, Tsai YC, Jones P, Summerhayes I, Marshall F, Paul M, Green P, Hamilton SR, Frost P, Vogelstein B (1991) Identification of p53 gene mutations in bladder cancers and urine samples. Science 252:706

    Google Scholar 

  25. Tabin CJ, Bradley SM, Bargmann CI, Weinberg RA, Papageorge AG, Scolnick EM, Dhar R, Lowy DR, Chang EH (1982) Mechanism of activation of a human oncogene. Nature 300:143

    Google Scholar 

  26. Talaska G, Al-Juburi AZSS, Kadlubar FF (1991) Smoking related carcinogen-DNA adducts in biopsy samples of human urinary bladder: identification of N-(deoxy guanosin-8-yl)-4-aminobiphenyl as a major adduct. Proc Natl Acad Sci USA 88:5350

    Google Scholar 

  27. Taparowsky E, Suard Y, Fasano O, Shimizu K, Goldfarb M, Wigler M (1982) Activation of T24 bladder carcinoma transforming gene is linked to a single amino acid change. Nature 300:762

    Google Scholar 

  28. Vogelstein B, Fearon ER, Hamilton SR, Kern SE, Preisinger AC, Leppert M, Nakamura Y, White R, Smits AMM, Bos JL (1988) Genetic alterations during colorectal-tumor development. N Engl J Med 319:525

    Google Scholar 

  29. United States Department of Health, Education and Welfare (1979) Smoking and Health. Report of the Surgeon General. In: Department of Health, Education and Welfare Publication No. (PHS) 79-50066. Government Printing Office, Washington DC, p 35

    Google Scholar 

  30. Wiseman RW, Stowers SJ, Miller EC, Anderson MW, Miller JA (1986) Activating mutations of the c-Ha-ras protooncogene in chemically induced hepatomas of the male B6C3F1 mouse. Proc Natl Acad Sci USA 83:5825

    Google Scholar 

  31. Zarbl H, Sukumar S, Arthur AV, Martin-Zanca D, Barbacid M (1985) Direct mutagenesis of H-ras-1 oncogens by nitrosomethylurea during initiation of mammary carcinogenesis in rats. Nature 315:382

    Google Scholar 

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Takenawa, J., Okumura, K., Yoshida, O. et al. Urinary excretion of mutagens and covalent DNA damage induced in the bladder and kidney after passive smoking in rats. Urol Res 22, 93–97 (1994). https://doi.org/10.1007/BF00310998

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  • DOI: https://doi.org/10.1007/BF00310998

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