Genotoxicity of furan in Big Blue rats

► We evaluated the cancer mode of action for furan. ► The systemic and liver genotoxicity of furan was evaluated in Big Blue rats. ► Most genotoxicity assays were negative. ► We conclude that furan has a predominantly nongenotoxic cancer mode of action. Furan is a multispecies liver carcinogen whose...

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Published in:Mutation research. Genetic toxicology and environmental mutagenesis 2012-02, Vol.742 (1), p.72-78
Main Authors: McDaniel, L. Patrice, Ding, Wei, Dobrovolsky, Vasily N., Shaddock, Joseph G., Mittelstaedt, Roberta A., Doerge, Daniel R., Heflich, Robert H.
Format: Article
Language:English
Subjects:
Bioassays
Cancer mode of action
Carcinogens
Chemical compounds
Comet assay
Cytotoxicity
DNA damage
Hprt mutation
Micronucleus assay
Pig-a mutation
Rodents
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Summary:► We evaluated the cancer mode of action for furan. ► The systemic and liver genotoxicity of furan was evaluated in Big Blue rats. ► Most genotoxicity assays were negative. ► We conclude that furan has a predominantly nongenotoxic cancer mode of action. Furan is a multispecies liver carcinogen whose cancer mode of action (MOA) is unclear. A major metabolite of furan is a direct acting mutagen; however, it is not known if genotoxicity is a key step in the tumors that result from exposure to furan. In order to address this question, transgenic Big Blue rats were treated by gavage five times a week for 8 weeks with two concentrations of furan used in cancer bioassays (2 and 8 mg/kg), and with two higher concentrations (16 and 30 mg/kg). Peripheral blood samples taken 24 h after the 5th dose (1 week of dosing) were used to assay for micronucleus (MN) frequency in normochromatic erythrocytes (NCEs) and reticulocytes (RETs), and Pig-a gene mutation in total red blood cells (RBCs). 24 h after the last dose of the 8-week treatment schedule, the rats were euthanized, and their tissues were used to perform NCE and RET MN assays, the Pig-a RBC assay, Pig-a and Hprt lymphocyte gene mutation assays, the liver cII transgene mutation assay, and the liver Comet assay. The responses in the MN assays conducted at both sampling times, and all the gene mutation assays, were uniformly negative; however, the Comet assay was positive for the induction of liver DNA damage. As the positive responses in the Comet assay were seen only with doses in excess of the cancer bioassay doses, and at least one of these doses (30 mg/kg) produced toxicity in the liver, the overall findings from the study are consistent with furan having a predominantly nongenotoxic MOA for cancer.
ISSN:1383-5718
1879-3592
DOI:10.1016/j.mrgentox.2011.12.011