Fluoro-substituted N-nitrosamines. 2. Metabolism of N-nitrosodiethylamine and of fluorinated analogs in liver microsomal fractions
- 1 January 1982
- journal article
- research article
- Published by Oxford University Press (OUP) in Carcinogenesis: Integrative Cancer Research
- Vol. 3 (2) , 155-159
- https://doi.org/10.1093/carcin/3.2.155
Abstract
High densities of wild-type, 6-thioguanine sensitive V79 cells reduce the recovery of 6-thioguanine resistant (6TGR) cells when they are co-cultivated. This metabolic co-operation effect has been reported previously to be eliminated by the tumour promoter 12-O-tetradecanoylphorbol-13-acetate and the accompanying enhancement of 6TGR colony recovery has been postulated as a rapid assay for tumour promoters. Elimination of metabolic co-operation, however, does not appear to be a characteristic of either the promoting agents anthralin, iodoacetic acid, oleic acid and δ-haemolysin or the co-carcinogenic/carcinogenic agents griseofulvin, diethyl-stilboestrol and stilboestrol diproprionate. Moreover, with the exception of stilboestrol diproprionate, none of these agents induce sister chromatid exchanges, but are all, with the exception of δ-haemolysin, associated with limited numerical chromosome changes and in four cases low level aberration induction. None of the agents were mutagenic.This publication has 4 references indexed in Scilit:
- Fluoro-substituted N-nitrosamines. 1. Inactivity of N-nitrosobis(2,2,2-trifluoroethyl)amine in carcinogenicity and mutagenicity testsCarcinogenesis: Integrative Cancer Research, 1981
- Metabolism of formaldehyde during in vitro drug demethylationBiochemical Pharmacology, 1980
- Denitrosation of N-nitrosomorpholine by liver microsomes; Possible role of cytochrome P-450Cancer Letters, 1980
- Liposolubility as an aspect of nitrosamine carcinogenicity: Quantitative correlations and qualitative observationsChemico-Biological Interactions, 1977