Literature DB >> 10898583

A reactive metabolite of furan, cis-2-butene-1,4-dial, is mutagenic in the Ames assay.

L A Peterson1, K C Naruko, D P Predecki.   

Abstract

Furan is classified as a nongenotoxic hepatocarcinogen. It is thought to be activated to a toxic metabolite, cis-2-butene-1,4-dial, which is acutely toxic to liver cells. The resulting cytotoxicity is followed by compensatory cell proliferation, increasing the likelihood of tumor production. We examined the genotoxic activity of cis-2-butene-1,4-dial in several strains of Salmonella typhimurium commonly used in the Ames assay. This reactive compound tested positive in TA104, a strain that is sensitive to aldehydes. Mutagenic activity was concentration-dependent (1000 +/- 180 revertants/micromol). Incubation of cis-2-butene-1,4-dial with glutathione prior to addition of bacteria inhibited both the acute toxic and genotoxic activity of this compound. No evidence of mutagenic activity was seen at nontoxic concentrations in TA97, TA98, TA100, and TA102. Our findings are consistent with the hypothesis that cis-2-butene-1,4-dial reacts with DNA to form mutagenic adducts. Our data suggest that cis-2-butene-1,4-dial may be an important genotoxic as well as toxic intermediate in furan-induced tumorigenesis.

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Year:  2000        PMID: 10898583     DOI: 10.1021/tx000065f

Source DB:  PubMed          Journal:  Chem Res Toxicol        ISSN: 0893-228X            Impact factor:   3.739


  18 in total

1.  Identification of a cis-2-butene-1,4-dial-derived glutathione conjugate in the urine of furan-treated rats.

Authors:  Lisa A Peterson; Meredith E Cummings; Jacqueline Y Chan; Choua C Vu; Brock A Matter
Journal:  Chem Res Toxicol       Date:  2006-09       Impact factor: 3.739

2.  Detection of DNA adducts derived from the reactive metabolite of furan, cis-2-butene-1,4-dial.

Authors:  Michael C Byrns; Choua C Vu; Jonathan W Neidigh; José-Luis Abad; Roger A Jones; Lisa A Peterson
Journal:  Chem Res Toxicol       Date:  2006-03       Impact factor: 3.739

3.  Comparative metabolism of furan in rodent and human cryopreserved hepatocytes.

Authors:  Leah A Gates; Martin B Phillips; Brock A Matter; Lisa A Peterson
Journal:  Drug Metab Dispos       Date:  2014-04-21       Impact factor: 3.922

4.  Formation of 1,4-dioxo-2-butene-derived adducts of 2'-deoxyadenosine and 2'-deoxycytidine in oxidized DNA.

Authors:  Bingzi Chen; Choua C Vu; Michael C Byrns; Peter C Dedon; Lisa A Peterson
Journal:  Chem Res Toxicol       Date:  2006-08       Impact factor: 3.739

5.  Mutagenicity of furan in female Big Blue B6C3F1 mice.

Authors:  Ashley N Terrell; Mailee Huynh; Alex E Grill; Ramesh C Kovi; M Gerard O'Sullivan; Joseph B Guttenplan; Yen-Yi Ho; Lisa A Peterson
Journal:  Mutat Res Genet Toxicol Environ Mutagen       Date:  2014-06-02       Impact factor: 2.873

6.  Low dose assessment of the carcinogenicity of furan in male F344/N Nctr rats in a 2-year gavage study.

Authors:  Linda S Von Tungeln; Nigel J Walker; Greg R Olson; Maria C B Mendoza; Robert P Felton; Brett T Thorn; M Matilde Marques; Igor P Pogribny; Daniel R Doerge; Frederick A Beland
Journal:  Food Chem Toxicol       Date:  2016-11-18       Impact factor: 6.023

7.  Trapping of cis-2-butene-1,4-dial to measure furan metabolism in human liver microsomes by cytochrome P450 enzymes.

Authors:  Leah A Gates; Ding Lu; Lisa A Peterson
Journal:  Drug Metab Dispos       Date:  2011-12-20       Impact factor: 3.922

8.  Degraded protein adducts of cis-2-butene-1,4-dial are urinary and hepatocyte metabolites of furan.

Authors:  Ding Lu; Mathilde M Sullivan; Martin B Phillips; Lisa A Peterson
Journal:  Chem Res Toxicol       Date:  2009-06       Impact factor: 3.739

Review 9.  Reactive metabolites in the biotransformation of molecules containing a furan ring.

Authors:  Lisa A Peterson
Journal:  Chem Res Toxicol       Date:  2012-10-24       Impact factor: 3.739

10.  Covalent modification of cytochrome c by reactive metabolites of furan.

Authors:  Martin B Phillips; Mathilde M Sullivan; Peter W Villalta; Lisa A Peterson
Journal:  Chem Res Toxicol       Date:  2013-12-23       Impact factor: 3.739

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