Mutation frequency in the lac1 gene of liver DNA from lambda/lac1 transgenic mice following the interaction of PCBs with iron causing hepatic cancer and porphyria

Citation
R. Davies et al., Mutation frequency in the lac1 gene of liver DNA from lambda/lac1 transgenic mice following the interaction of PCBs with iron causing hepatic cancer and porphyria, MUTAGENESIS, 15(5), 2000, pp. 379-383
Citations number
34
Categorie Soggetti
Molecular Biology & Genetics
Journal title
MUTAGENESIS
ISSN journal
02678357 → ACNP
Volume
15
Issue
5
Year of publication
2000
Pages
379 - 383
Database
ISI
SICI code
0267-8357(200009)15:5<379:MFITLG>2.0.ZU;2-0
Abstract
The synergistic interaction of iron overload, Ahr genotype and exposure to a mixture of polychlorinated biphenyls (PCBs) (Aroclor 1254) in mice leads to hepatic porphyria, oxidative DNA damage and cancer. In humans, hepatocel lular cancer is associated with iron overload and hepatic porphyria, Neithe r the mechanism of hepatic carcinogenesis induced by PCBs in rodents nor he patocellular cancer induced by iron and porphyria in humans are understood. To test the hypothesis that chronic interaction of iron and PCBs may induc e mutagenesis in liver DNA, lambda /lacI transgenic C57BL/6 mice were given iron dextran (600 mg iron/kg) and then administered Aroclor 1254 in the di et (0.01%) for 7 weeks. Hepatic iron, CYP1A activity and CYP1A1/1A2 protein were elevated >20-fold as a result of iron or Aroclor treatments, respecti vely, but porphyria with associated histological changes only developed in the combined iron/Aroclor treatment group, lambda/lacI shuttle vectors were isolated from liver genomic DNA and the mutational frequency (MF) in the l ad gene determined. Both iron and Aroclor treatments alone caused significa nt small increases in MF (1.5- and 1.4-fold, respectively), however, the MF following the combined iron and Aroclor treatment (1.6-fold) was not great er than the additive effects. In contrast, the MF was significantly elevate d (4.7-fold) in liver DNA of mice 2 weeks following five daily doses of N-n itrosodimethylamine (4 mg/kg), These studies demonstrate that neither PCBs nor iron overload caused marked point mutations even in a combination regim e that leads to oxidative damage and cancer, There was also no strong evide nce either that porphyrins or chronic CYP1A1 expression induced by the PCBs after this period caused marked point mutagens or simple deletions. Hence, to understand the PCBs-iron synergism more complex scenarios than point mu tations or simple deletions must be invoked.