Abstract |
A genetically engineered V79 cell line expressing rat CYP1A2 and another cell line expressing rat CYP1A2 as well as endogenous acetyltransferase activity, as well as CYP-deficient parental V79 cell lines, were used to assess the genotoxicity of the aromatic amines and amides 2-aminoanthracene, 2-aminofluorene, 2-acetylaminofluorene, 4-acetylaminofluorene and 2-amino-3-methylimidazo[4,5-f] quinoline, with chromosomal aberrations and sister chromatid exchanges as the end-points. None of the test compounds showed a clear effect on the frequency of chromosomal aberrations in any cell line used. Sister chromatid exchanges, however, were induced by 2-aminoanthracene, 2-aminofluorene and 2-acetylaminofluorene in the CYP1A2-proficient cells, but not in the CYP1A2-deficient cells. The presence of acetyltransferase activity enhanced the effect of 2-aminoanthracene, 2-aminofluorene and 2-acetylaminofluorene. 4-Acetylaminofluorene and 2-amino-3-methylimidazo[4,5-f] quinoline did not induce sister chromatid exchanges in the investigated cell lines. The use of cell lines with defined metabolic capabilities seems to be a valuable tool to study specific metabolic pathways important in the activation of procarcinogens.
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Authors | A S Rodrigues, I D Silva, M H Caria, A Laires, T Chaveca, H R Glatt, J Rueff |
Journal | Mutation research
(Mutat Res)
Vol. 341
Issue 2
Pg. 93-100
(Dec 1994)
ISSN: 0027-5107 [Print] Netherlands |
PMID | 7527492
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Anthracenes
- Fluorenes
- Mutagens
- Quinolines
- 2-amino-3-methylimidazo(4,5-f)quinoline
- 2-aminofluorene
- 2-anthramine
- Cytochrome P-450 Enzyme System
- 2-Acetylaminofluorene
- Oxidoreductases
- Cytochrome P-450 CYP1A2
- 4-acetylaminofluorene
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Topics |
- 2-Acetylaminofluorene
(analogs & derivatives, toxicity)
- Animals
- Anthracenes
(toxicity)
- Biotransformation
- Cell Line
- Chromosome Aberrations
- Cricetinae
- Cytochrome P-450 CYP1A2
- Cytochrome P-450 Enzyme System
(genetics, physiology)
- Fluorenes
(toxicity)
- Genetic Engineering
- Mutagenicity Tests
- Mutagens
(metabolism, toxicity)
- Oxidoreductases
(genetics, physiology)
- Quinolines
(toxicity)
- Rats
- Sister Chromatid Exchange
(drug effects)
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