## Abstract Four known carcinogenic compounds, all of which contain the nitroso group, have been found to be effective in producing cell killing, chromatid breaks, mutagenesis and chromatid rearrangements in Chinese hamster ovary cells. Single cell survival curves revealed these agents to exhibit a
Cell-mediated mutagenesis of mammalian cells with chemical carcinogens
✍ Scribed by Eliezer Huberman; Leo Sachs
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- French
- Weight
- 561 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0020-7136
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✦ Synopsis
Abstract
Chemically non‐reactive carcinogens, such as polycyclic hydrocarbons, have to be metabolized by cellular enzymes in order to exert their biological effects including mutagenicity. Chinese hamster V79 cells can be efficiently mutated from 8‐azaguanine susceptibility to resistance by N‐methyl‐N‐nitro‐N‐nitrosoguanidine. But these cells do not metabolize polycyclic hydrocarbons and were therefore not mutated by these compounds. A system of cell‐mediated mutagenesis with carcinogenic hydrocarbons has been developed, by co‐cultivating V79 cells with lethally irradiated rodent cells that can metabolize the carcinogens. The number of mutations was dependent on the number of metabolizing cells and the carcinogens were not mutagenic when V79 cells were co‐cultivated with non‐metabolizing cells. Inhibition of the hydrocarbon metabolizing enzymes by 7,8‐benzoflavone, inhibited mutagenicity. Cell‐mediated mutagenicity was obtained with the carcinogenic hydrocarbons 7,12‐dimethylbenz (a)anthracene, benzo(a)pyrene and 3‐methylcholanthrene and there was no mutagenicity with the non‐carcinogenic hydrocarbon benz(a)anthracene. The degree of mutagenicity was related to the degree of carcinogenicity and the method detected mutagenicity with 0.1μg/ml. It is suggested that cell‐mediated mutagenesis with human cells should provide a useful system to test for environmental chemicals hazardous to humans that have to be metabolically activated.
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The system previously described for inducing single gene mutations in Chinese hamster cells has been extended to produce additional auxotrophic mutants. An improved method for quantitating the efficiency of single gene mutation to specific auxotrophies has been developed. Mutagenesis in the forward
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract Three potycyclic hydrocarbons, benz(__a__)anthracene, 3‐methylcholanthrene and 7,12‐dimethyl‐benz(__a__)anthracene, have been studied in a cell‐mediated mutagenesis system using BHK 21 cells to metabolize the hydrocarbons and V‐79 cells as targets for detecting induced cytotoxicity and