Abstract
THE transformation of inactive or slightly active compounds into effective carcinogens by O-methylation has been discussed previously1, and it was suggested that endogenous carcinogens may possibly be formed by alkylation of normal cell constituents in the body. Such a mechanism could account also for the carcinogenic effects of radiation and of remotely acting agents, such as the azo-dyes, ethionine, etc., which may give rise to alkyl radicals in the body.
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References
Schoental, R., Nature, 182, 719 (1958).
Gutsche, C. D., Org. Reactions, 8, 364 (1954).
Bachmann, W. E., et al., J. Amer. Chem. Soc., 62, 824 (1940).
Shimkin, M. B., and Lorenz, E., J. Nat. Cancer Inst., 2, 499 (1942).
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SCHOENTAL, R. Carcinogenic Action of Diazomethane and of Nitroso-N-methyl Urethane. Nature 188, 420–421 (1960). https://doi.org/10.1038/188420b0
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DOI: https://doi.org/10.1038/188420b0
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