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Genotoxicity of three food processing contaminants in transgenic mice expressing human sulfotransferases 1A1 and 1A2 as assessed by the in vivo alkaline single cell gel electrophoresis assay
The food processing contaminants 2‐amino‐1‐methyl‐6‐phenylimidazo[4,5‐b]pyridine (PhIP), 5‐hydroxymethylfurfural (HMF) and 2,5 dimethylfuran (DMF) are potentially both mutagenic and carcinogenic in vitro and/or in vivo, although data on DMF is lacking. The PHIP metabolite N‐hydroxy‐PhIP and HMF are...
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Published in: | Environmental and molecular mutagenesis 2015-10, Vol.56 (8), p.709-714 |
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description | The food processing contaminants 2‐amino‐1‐methyl‐6‐phenylimidazo[4,5‐b]pyridine (PhIP), 5‐hydroxymethylfurfural (HMF) and 2,5 dimethylfuran (DMF) are potentially both mutagenic and carcinogenic in vitro and/or in vivo, although data on DMF is lacking. The PHIP metabolite N‐hydroxy‐PhIP and HMF are bioactivated by sulfotransferases (SULTs). The substrate specificity and tissue distribution of SULTs differs between species. A single oral dose of PhIP, HMF or DMF was administered to wild‐type (wt) mice and mice expressing human SULT1A1/1A2 (hSULT mice). DNA damage was studied using the in vivo alkaline single cell gel electrophoresis (SCGE) assay. No effects were detected in wt mice. In the hSULT mice, PhIP and HMF exposure increased the levels of DNA damage in the liver and kidney, respectively. DMF was not found to be genotoxic. The observation of increased DNA damage in hSULT mice compared with wt mice supports the role of human SULTs in the bioactivation of N‐hydroxy‐PhIP and HMF in vivo. Environ. Mol. Mutagen. 56:709–714, 2015. © 2015 The Authors. Environmental and Molecular Mutagenesis Published by Wiley Periodicals, Inc. |
doi_str_mv | 10.1002/em.21963 |
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The PHIP metabolite N‐hydroxy‐PhIP and HMF are bioactivated by sulfotransferases (SULTs). The substrate specificity and tissue distribution of SULTs differs between species. A single oral dose of PhIP, HMF or DMF was administered to wild‐type (wt) mice and mice expressing human SULT1A1/1A2 (hSULT mice). DNA damage was studied using the in vivo alkaline single cell gel electrophoresis (SCGE) assay. No effects were detected in wt mice. In the hSULT mice, PhIP and HMF exposure increased the levels of DNA damage in the liver and kidney, respectively. DMF was not found to be genotoxic. The observation of increased DNA damage in hSULT mice compared with wt mice supports the role of human SULTs in the bioactivation of N‐hydroxy‐PhIP and HMF in vivo. Environ. Mol. Mutagen. 56:709–714, 2015. © 2015 The Authors. Environmental and Molecular Mutagenesis Published by Wiley Periodicals, Inc.</description><identifier>ISSN: 0893-6692</identifier><identifier>EISSN: 1098-2280</identifier><identifier>DOI: 10.1002/em.21963</identifier><identifier>PMID: 26270892</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Administration, Oral ; Animals ; Arylsulfotransferase - genetics ; Brief Communication ; comet assay ; Comet Assay - methods ; DNA Breaks, Double-Stranded ; DNA cross linking ; DNA Damage ; DNA strand break ; Food Contamination ; Food Handling ; Furaldehyde - administration & dosage ; Furaldehyde - analogs & derivatives ; Furaldehyde - toxicity ; furan derivative ; Furans - administration & dosage ; Furans - toxicity ; heterocyclic amine ; Humans ; Imidazoles - administration & dosage ; Imidazoles - toxicity ; Male ; Mice, Transgenic ; Mutagenicity Tests - methods ; sulfotransferase</subject><ispartof>Environmental and molecular mutagenesis, 2015-10, Vol.56 (8), p.709-714</ispartof><rights>2015 The Authors. 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Mol. Mutagen</addtitle><description>The food processing contaminants 2‐amino‐1‐methyl‐6‐phenylimidazo[4,5‐b]pyridine (PhIP), 5‐hydroxymethylfurfural (HMF) and 2,5 dimethylfuran (DMF) are potentially both mutagenic and carcinogenic in vitro and/or in vivo, although data on DMF is lacking. The PHIP metabolite N‐hydroxy‐PhIP and HMF are bioactivated by sulfotransferases (SULTs). The substrate specificity and tissue distribution of SULTs differs between species. A single oral dose of PhIP, HMF or DMF was administered to wild‐type (wt) mice and mice expressing human SULT1A1/1A2 (hSULT mice). DNA damage was studied using the in vivo alkaline single cell gel electrophoresis (SCGE) assay. No effects were detected in wt mice. In the hSULT mice, PhIP and HMF exposure increased the levels of DNA damage in the liver and kidney, respectively. DMF was not found to be genotoxic. The observation of increased DNA damage in hSULT mice compared with wt mice supports the role of human SULTs in the bioactivation of N‐hydroxy‐PhIP and HMF in vivo. Environ. Mol. Mutagen. 56:709–714, 2015. © 2015 The Authors. Environmental and Molecular Mutagenesis Published by Wiley Periodicals, Inc.</description><subject>Administration, Oral</subject><subject>Animals</subject><subject>Arylsulfotransferase - genetics</subject><subject>Brief Communication</subject><subject>comet assay</subject><subject>Comet Assay - methods</subject><subject>DNA Breaks, Double-Stranded</subject><subject>DNA cross linking</subject><subject>DNA Damage</subject><subject>DNA strand break</subject><subject>Food Contamination</subject><subject>Food Handling</subject><subject>Furaldehyde - administration & dosage</subject><subject>Furaldehyde - analogs & derivatives</subject><subject>Furaldehyde - toxicity</subject><subject>furan derivative</subject><subject>Furans - administration & dosage</subject><subject>Furans - toxicity</subject><subject>heterocyclic amine</subject><subject>Humans</subject><subject>Imidazoles - administration & dosage</subject><subject>Imidazoles - toxicity</subject><subject>Male</subject><subject>Mice, Transgenic</subject><subject>Mutagenicity Tests - methods</subject><subject>sulfotransferase</subject><issn>0893-6692</issn><issn>1098-2280</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNp1kluLEzEUgAdR3LoK_gIJ-OJL11zmlhdhLWsVV2VR8TGcZs602c0kNZmpnT_nbzPtdusFhJBAzpfvnBNOlj1l9IxRyl9id8aZLMW9bMKorKec1_R-NqG1FNOylPwkexTjNaWM5ZI_zE54yasU5JPs5xyd7_3WaNOPxLekXwVE0nrfkHXwGmM0bkm0dz10xoHrIzGO9AFcXKIzmnRGI8HtOhzQ1dCBI3Gwrd9TLQaIGAk7ZwRck05OIKaVLiM2ZDGmnLiTbszGE7A3YI1DspNZJBqtJUu0BC3qPvj1yqdMZi-A8XH2oAUb8cnhPM2-vrn4Mns7vfw0fzc7v5zqokp_IGFR1HXeyCLHFirBORWsZHkrRSGBMV3TBcWyFdCCFgsppeBSVnl6BFpjI06zV7fe9bDosNHoUm9WrYPpIIzKg1F_R5xZqaXfqILmnFGWBC8OguC_Dxh71Zm46w0c-iEqloqqGc-rMqHP_0Gv_RBcai9RnDORtvq3UAcfY8D2WAyjajcUCju1H4qEPvuz-CN4NwUJmN4CP4zF8b8idfHhTnjgTexxe-Qh3KiyElWhvn2cq_ev8_rqqpipz-IXI2HTVA</recordid><startdate>201510</startdate><enddate>201510</enddate><creator>Høie, Anja Hortemo</creator><creator>Svendsen, Camilla</creator><creator>Brunborg, Gunnar</creator><creator>Glatt, Hansruedi</creator><creator>Alexander, Jan</creator><creator>Meinl, Walter</creator><creator>Husøy, Trine</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><general>John Wiley and Sons Inc</general><scope>BSCLL</scope><scope>24P</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>7TM</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>5PM</scope></search><sort><creationdate>201510</creationdate><title>Genotoxicity of three food processing contaminants in transgenic mice expressing human sulfotransferases 1A1 and 1A2 as assessed by the in vivo alkaline single cell gel electrophoresis assay</title><author>Høie, Anja Hortemo ; Svendsen, Camilla ; Brunborg, Gunnar ; Glatt, Hansruedi ; Alexander, Jan ; Meinl, Walter ; Husøy, Trine</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5793-9ab5884d954efa7322031614f9359a11c80b0e6f3afac3b999329974588acced3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Administration, Oral</topic><topic>Animals</topic><topic>Arylsulfotransferase - genetics</topic><topic>Brief Communication</topic><topic>comet assay</topic><topic>Comet Assay - methods</topic><topic>DNA Breaks, Double-Stranded</topic><topic>DNA cross linking</topic><topic>DNA Damage</topic><topic>DNA strand break</topic><topic>Food Contamination</topic><topic>Food Handling</topic><topic>Furaldehyde - administration & dosage</topic><topic>Furaldehyde - analogs & derivatives</topic><topic>Furaldehyde - toxicity</topic><topic>furan derivative</topic><topic>Furans - administration & dosage</topic><topic>Furans - toxicity</topic><topic>heterocyclic amine</topic><topic>Humans</topic><topic>Imidazoles - administration & dosage</topic><topic>Imidazoles - toxicity</topic><topic>Male</topic><topic>Mice, Transgenic</topic><topic>Mutagenicity Tests - methods</topic><topic>sulfotransferase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Høie, Anja Hortemo</creatorcontrib><creatorcontrib>Svendsen, Camilla</creatorcontrib><creatorcontrib>Brunborg, Gunnar</creatorcontrib><creatorcontrib>Glatt, Hansruedi</creatorcontrib><creatorcontrib>Alexander, Jan</creatorcontrib><creatorcontrib>Meinl, Walter</creatorcontrib><creatorcontrib>Husøy, Trine</creatorcontrib><collection>Istex</collection><collection>Wiley Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Environmental and molecular mutagenesis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Høie, Anja Hortemo</au><au>Svendsen, Camilla</au><au>Brunborg, Gunnar</au><au>Glatt, Hansruedi</au><au>Alexander, Jan</au><au>Meinl, Walter</au><au>Husøy, Trine</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genotoxicity of three food processing contaminants in transgenic mice expressing human sulfotransferases 1A1 and 1A2 as assessed by the in vivo alkaline single cell gel electrophoresis assay</atitle><jtitle>Environmental and molecular mutagenesis</jtitle><addtitle>Environ. Mol. Mutagen</addtitle><date>2015-10</date><risdate>2015</risdate><volume>56</volume><issue>8</issue><spage>709</spage><epage>714</epage><pages>709-714</pages><issn>0893-6692</issn><eissn>1098-2280</eissn><abstract>The food processing contaminants 2‐amino‐1‐methyl‐6‐phenylimidazo[4,5‐b]pyridine (PhIP), 5‐hydroxymethylfurfural (HMF) and 2,5 dimethylfuran (DMF) are potentially both mutagenic and carcinogenic in vitro and/or in vivo, although data on DMF is lacking. The PHIP metabolite N‐hydroxy‐PhIP and HMF are bioactivated by sulfotransferases (SULTs). The substrate specificity and tissue distribution of SULTs differs between species. A single oral dose of PhIP, HMF or DMF was administered to wild‐type (wt) mice and mice expressing human SULT1A1/1A2 (hSULT mice). DNA damage was studied using the in vivo alkaline single cell gel electrophoresis (SCGE) assay. No effects were detected in wt mice. In the hSULT mice, PhIP and HMF exposure increased the levels of DNA damage in the liver and kidney, respectively. DMF was not found to be genotoxic. The observation of increased DNA damage in hSULT mice compared with wt mice supports the role of human SULTs in the bioactivation of N‐hydroxy‐PhIP and HMF in vivo. Environ. Mol. Mutagen. 56:709–714, 2015. © 2015 The Authors. Environmental and Molecular Mutagenesis Published by Wiley Periodicals, Inc.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>26270892</pmid><doi>10.1002/em.21963</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Administration, Oral Animals Arylsulfotransferase - genetics Brief Communication comet assay Comet Assay - methods DNA Breaks, Double-Stranded DNA cross linking DNA Damage DNA strand break Food Contamination Food Handling Furaldehyde - administration & dosage Furaldehyde - analogs & derivatives Furaldehyde - toxicity furan derivative Furans - administration & dosage Furans - toxicity heterocyclic amine Humans Imidazoles - administration & dosage Imidazoles - toxicity Male Mice, Transgenic Mutagenicity Tests - methods sulfotransferase |
title | Genotoxicity of three food processing contaminants in transgenic mice expressing human sulfotransferases 1A1 and 1A2 as assessed by the in vivo alkaline single cell gel electrophoresis assay |
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