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Eppley Institute for Research in Cancer, University of Nebraska Medical Center, Omaha, Nebraska 68105 [P. P., J. A., R. G., R. K.]; Institut für Toxikologie und Chemotherapie, Deutsches Krebsforschungszentrum, Heidelberg, West Germany [F. K.]; and Abteilung für Experimentelle Pathologie, Medizinische Hochschule Hannover, Hannover, Germany [U. M.]
N-Nitroso-bis(2-acetoxypropyl)amine, a possible ß metabolite of N-nitroso-di-n-propylamine, was shown to be a potent carcinogen in the Syrian golden hamster. After a single s.c. treatment, the pancreas was the most affected organ, followed by the liver, respiratory tract, and kidneys. However, repeated application resulted in a higher incidence of neoplasms of the respiratory tract than of the pancreas and kidneys. The effect of N-nitroso-bis(2-acetoxypropyl)amine on toxicity, target tissues, and carcinogenicity was similar to that of N-nitroso-bis(2-hydroxypropyl)amine. The assumption that these two compounds may have similar metabolic pathways was confirmed; N-nitrosobis(2-acetoxypropyl)amine was readily deesterified to N-nitroso-bis(2-hydroxypropyl)amine in vivo and in vitro.
1 Supported by USPHS Contract NO1 CP33278 from the National Cancer Institute, NIH.
2 To whom requests for reprints should be addressed, at Eppley Institute for Research in Cancer, University of Nebraska Medical Center, 42nd Street and Dewey Avenue, Omaha, Nebr. 68105.
Received 2/ 5/76. Accepted 4/29/76.
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