Abstract
In humans and experimental animals, carcinogenesis is a complex process in which normal cell growth is modified. Carcinogenesis is divided into three main stages: initiation, promotion and progression. Chemopreventive interaction in carcinogenesis offers two major strategies. The first strategy will inhibit or at least slow down carcinogenesis by blocking its progress. This might occurr at all stages of carcinogenesis. This strategy includes the scavenging of bioreactive intermediates (BRIs), induction or inhibition of enzymes of the metabolism of xenobiotics which create or detoxify the BRIs, of enzymes of DNA-repair or of other enzymes. A second strategy aims at reversing the process of tumour formation either by redifferentiation of transformed cells or the elimination of precarcinogenic clones. Both strategies cover one or several steps of carcinogenesis and approach the subject matter in more general terms without consideration of individual susceptibility to particular cancers (Kelloff et al., 1999).
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References
Appel, K.E., Peter, H., and Bolt, H.M., 1981, Effect of potential antidotes on the acute toxicity of acrylonitrile Int. Arch. Occup. Environ. Hlth 49:157.
Benz, F.W., Nerland, D.E., Corbett, D., and Li, J., 1997, Biological markers of acute acrylonitrile intoxication as a function of dose and time Fundam. Appl. Toxicol. 36:141.
Benz, F.W., Nerland, D.E., Li, J., and Corbett, D., 1997a, Dose dependence of covalent binding of acrylonitrile to tissue protein and globin in rats Fundam. Appl. Toxicol. 36:149.
Buchter, A. and Peter, H. 1984, Clinical toxicology of acrylonitrile. G. Ital. Med. Lay. 6:83.
Buchter, A., Peter, H., and Bolt, H.M., 1984, N-Acetyl-Cystein als Antidot bei akzidenteller AcrylnitrilIntoxikation Int. Arch. Occup. Environ. Hlth 53:311.
DFG, 1983, Head-Space-Technik (Dampfraumanalyse), in: Analytische Methoden zur Prüfung gesundheitsschädlicher Arbeitsstoffe. Analysen im biologischen Material, Band 2, 7. Lieferung, pp. D1–D2, VCH, Weinheim.
DFG, 1988, Cyanid, in: Analytische Methoden zur Prüfung gesundheitsschädlicher Arbeitsstoffe, Analysen im biologischen Material, Band 2, 9. Lieferung, pp. D1–D3, VCH, Weinheim.
DFG, 1996, N-2-Cyanoethyl-Valin, N-2-Hydroxyethyl-Valin, N-Methyl-Valin (zum Nachweis einer BelastungBeanspruchung durch Acrylnitril, Ethylenoxid sowie methylierende Substanzen, in:Analytische Methoden zur Prüfung gesundheitsschädlicher Arbeitsstoffe. Analysen im biologischen Material, Band 2, 12. Lieferung, pp. D1–D9, VCH, Weinheim.
Fennell, T.R., Kedderis, G.L., and Sumner, S.C.J., 1991, Urinary metabolites of [1,2,3-13C]acrylonitrile in rats and mice detected by13C nuclear magnetic resonance spectroscopy Chem. Res. Toxicol. 4:678.
Gansewendt, B., Foest, U., Xu, D., Hallier, E., Bolt, H.M., and Peter, H., 1991, Formation of DNA adducts in F-344 rats after oral administration or inhalation of [“C]methyl bromide Food Chem. Toxicol. 29:557.
Gamier, R., Rambourg-Schepens, M.O., Muller, A., and Hallier, E., 1996, Glutathione transferase activity and formation of macromolecular adducts in two cases of acute methyl bromide poisoning, Occup. Environ. Med. 53:211.
Harries, L.W., Stubbins, M.J., Forman, D., Howard, G.C.W., and Wolf, C.R., 1997, Identification of genetic polymorphisms at the glutathione S-transferase Pi locus and association with susceptibility to bladder, testicular and prostate cancer Carcinogenesis 18:641.
Harris, M.J., Coggan, M., Langton, L., Wilson, S.R., and Board, P.G., 1998, Polymorphism of the Pi class glutathione S-transferase in normal populations and cancer patients Pharmacogenetics 8:27.
Hirvonen, A., Bouchardy, C., Mitrunen, K., Kataja, V., Eskelinen, M., Kosma, V.M., Saarikoski, S.T., Jourenkova, N., Anttila, S., Dayer, P., Uusitupa, M., and Benhamou, S., 2000, Polymorphic GSTs and cancer predispotiotion, In: GST 2000, International Conference on Glutathione Transferases, Uppsala, Sweden, Abstract Book: L10.
IARC, 1999, Acrylonitrile, in: IARC Monographs on the Evaluation of Carcinogenic Risks to humans, IARC, Lyon.
Kedderis G.L., Sumner S.C.J., Held S.D., Batra R., Turner Jr. M.J., Roberts A.E., and Fennell T.R., 1993, Dose-dependent urinary excretion of acrylonitrile metabolites by rats and mice Toxicol. Appl. Pharmacol. 120:288.
Kelloff, G.J., Sigman, C.C., and Greenwal, P., 1999, Cancer chemoprevention: progress and promise Eur. J. Cancer 35:2031.
Lewalter J., 1996, N-Alkylvaline levels in globin as a new type of biomarker in risk assessment of alkylating agents Int. Arch. Occup. Environ. Hlth 68:519.
Lewalter J. and Neumann H.G., 1998, Biologische Arbeitsstoff-Toleranzwerte (Biomonitoring). Teil XII. Die Bedeutung der individuellen Empfindlichkeit beim Biomonitoring Arbeitsmed. Sozialmed. Umwelmed. 33:352.
MEDITEXT (R) Medical Management, 1996, Acrylonitrile, in: System A.H. Hall and B.H. Rumack, eds. MICROMEDEX, Inc.: Englewood, CO, USA
Peter H. and Bolt H.M., 1981, Irreversible protein binding of acrylonitrile Xenobiotica 11:51.
Peter H., Schwarz M., Mathiasch B., Appel K.E., Bolt H.M., 1983, A note on synthesis and reactivity towards DNA of glycidonitrile, the epoxide of acrylonitrile Carcinogenesis 4:235.
Peter H. and Bolt, H.M., 1984, Experimental pharmacokinetics and toxicology of acrylonitrile G. Ital. Med. Lay. 6:77.
Recio L. and Skopek T.R., 1988, Mutagenicity of acrylonitrile and its metabolite 2-cyanoethylene oxide in human lymphoblaste in vitro Mut. Res. 206:297.
Steffens, W., Sibbing, D., Kiesselbach, N., and Lewalter, J., 1998, Behandlung von Patienten mit Vergiftungen durch aliphatische oder olefinische Nitrile Arbeitsmed. Sozialmed. Umweltmed. 33:11.
Thier R., Lewalter J., Kempkes M., Selinski S., Brüning T., and Bolt H.M., 1999, Haemoglobin adducts of acrylonitrile and ethylene oxide in acrylonitrile workers, dependent on polymorphisme of the glutathione transferases GSTTI and GSTM1 Arch. Toxicol. 73:197.
Yamamoto K., Yamamoto Y., and Kuwahara C., 1979, A blood cyanide distribution study in the rabbits intoxicated by oral route and by inhalation Z. Rechtsmed. 83:313.
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Thier, R. (2001). Chemoprotection and Interindividual Differences in Response to Biological Reactive Intermediates. In: Dansette, P.M., et al. Biological Reactive Intermediates VI. Advances in Experimental Medicine and Biology, vol 500. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-0667-6_87
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DOI: https://doi.org/10.1007/978-1-4615-0667-6_87
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