4.4 Article Proceedings Paper

Electrophilic intermediates produced by bioactivation of furan

Journal

DRUG METABOLISM REVIEWS
Volume 38, Issue 4, Pages 615-626

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/03602530600959417

Keywords

furan; carcinogenesis; toxicity; metabolism; glutathione conjugates; stable isotope methods; alpha,beta-unsaturated aldehyde

Funding

  1. NIEHS NIH HHS [ES-10577, ES-10956] Funding Source: Medline
  2. NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES [T32ES010956, R01ES010577] Funding Source: NIH RePORTER

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The industrial and environmental chemical, furan, is a liver toxicant and carcinogen in laboratory animals. It has been classified as a possible human carcinogen. The mechanism of tumor induction is unknown. However, toxicity is initiated by cytochrome P450 catalyzed oxidation of furan to an alpha,beta-unsaturated dialdehyde, cis-2-butene-1,4-dial This metabolite reacts readily with protein and DNA nucleophiles and is a bacterial mutagen in Ames assay strain TA104. Metabolism studies indicate that this reactive metabolite is formed in vivo. It is also an intermediate leading to other metabolites whose role in furan-derived toxicities has yet to be explored.

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