Dose-dependent synergistic and antagonistic mutation responses of binary mixtures of the environmental carcinogen benzo[a]pyrene with food-derived carcinogens
Cooking food at high temperatures produces genotoxic chemicals and there is concern about their impact on human health. DNA damage caused by individual chemicals has been investigated but few studies have examined the consequences of exposure to mixtures as found in food. The current study examined...
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description | Cooking food at high temperatures produces genotoxic chemicals and there is concern about their impact on human health. DNA damage caused by individual chemicals has been investigated but few studies have examined the consequences of exposure to mixtures as found in food. The current study examined the mutagenic response to binary mixtures of benzo[a]pyrene (BaP) with glycidamide (GA), BaP with acrylamide (AC), or 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) with GA at human-relevant concentrations (sub-nM). The metabolically competent human MCL-5 cells were exposed to these chemicals individually or in mixtures and mutagenicity was assessed at the thymidine kinase (TK) locus. Mixture exposures gave dose–responses that differed from those for the individual chemicals; for the BaP-containing mixtures, an increased mutation frequency (MF) at low concentration combinations that were not mutagenic individually, and decreased MF at higher concentration combinations, compared to the calculated predicted additive MF of the individual chemicals. In contrast, the mixture of PhIP with GA did not increase MF above background levels. These data suggest BaP is driving the mutation response and that metabolic activation plays a role; in mixtures with BaP the increased/decreased MF above/below the expected additive MF the order is PhIP > AC > GA. The increase in MF at some low concentration combinations that include BaP is interesting and supports our previous work showing a similar response for BaP with PhIP, confirming this response is not limited to the BaP/PhIP combination. Moreover, the lack of a mutation response for PhIP with GA relative to the response of the individual chemicals at equivalent doses is interesting and may represent a potential avenue for reducing the risk of exposure to environmental carcinogens; specifically, removal of BaP from the mixture may reduce the mutation effect, although in the context of food this would be significantly challenging. |
doi_str_mv | 10.1007/s00204-018-2319-4 |
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DNA damage caused by individual chemicals has been investigated but few studies have examined the consequences of exposure to mixtures as found in food. The current study examined the mutagenic response to binary mixtures of benzo[a]pyrene (BaP) with glycidamide (GA), BaP with acrylamide (AC), or 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) with GA at human-relevant concentrations (sub-nM). The metabolically competent human MCL-5 cells were exposed to these chemicals individually or in mixtures and mutagenicity was assessed at the thymidine kinase (TK) locus. Mixture exposures gave dose–responses that differed from those for the individual chemicals; for the BaP-containing mixtures, an increased mutation frequency (MF) at low concentration combinations that were not mutagenic individually, and decreased MF at higher concentration combinations, compared to the calculated predicted additive MF of the individual chemicals. In contrast, the mixture of PhIP with GA did not increase MF above background levels. These data suggest BaP is driving the mutation response and that metabolic activation plays a role; in mixtures with BaP the increased/decreased MF above/below the expected additive MF the order is PhIP > AC > GA. The increase in MF at some low concentration combinations that include BaP is interesting and supports our previous work showing a similar response for BaP with PhIP, confirming this response is not limited to the BaP/PhIP combination. Moreover, the lack of a mutation response for PhIP with GA relative to the response of the individual chemicals at equivalent doses is interesting and may represent a potential avenue for reducing the risk of exposure to environmental carcinogens; specifically, removal of BaP from the mixture may reduce the mutation effect, although in the context of food this would be significantly challenging.</description><identifier>ISSN: 0340-5761</identifier><identifier>EISSN: 1432-0738</identifier><identifier>DOI: 10.1007/s00204-018-2319-4</identifier><identifier>PMID: 30259071</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Acrylamide ; Background levels ; Baseline studies ; Benzo(a)pyrene ; Binary mixtures ; Biomedical and Life Sciences ; Biomedicine ; Carcinogens ; Chemical damage ; Chemicals ; Cooking ; Deoxyribonucleic acid ; DNA ; DNA damage ; Environmental Health ; Exposure ; Food ; Genotoxic chemicals ; Genotoxicity ; High temperature ; Impact damage ; Metabolic activation ; Metabolic rate ; Mutagenicity ; Mutation ; Occupational health ; Occupational Medicine/Industrial Medicine ; Organic chemistry ; Pharmacology/Toxicology ; Pyrene ; Pyridines ; Regulatory Toxicology ; Thymidine ; Thymidine kinase</subject><ispartof>Archives of toxicology, 2018-12, Vol.92 (12), p.3459-3469</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2018</rights><rights>Archives of Toxicology is a copyright of Springer, (2018). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-78207c8d0339f65e7aaf47793b8eb9ab250095812bafa9f740d584a5407deb33</citedby><cites>FETCH-LOGICAL-c415t-78207c8d0339f65e7aaf47793b8eb9ab250095812bafa9f740d584a5407deb33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00204-018-2319-4$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00204-018-2319-4$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30259071$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>David, Rhiannon M.</creatorcontrib><creatorcontrib>Gooderham, Nigel J.</creatorcontrib><title>Dose-dependent synergistic and antagonistic mutation responses of binary mixtures of the environmental carcinogen benzo[a]pyrene with food-derived carcinogens</title><title>Archives of toxicology</title><addtitle>Arch Toxicol</addtitle><addtitle>Arch Toxicol</addtitle><description>Cooking food at high temperatures produces genotoxic chemicals and there is concern about their impact on human health. DNA damage caused by individual chemicals has been investigated but few studies have examined the consequences of exposure to mixtures as found in food. The current study examined the mutagenic response to binary mixtures of benzo[a]pyrene (BaP) with glycidamide (GA), BaP with acrylamide (AC), or 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) with GA at human-relevant concentrations (sub-nM). The metabolically competent human MCL-5 cells were exposed to these chemicals individually or in mixtures and mutagenicity was assessed at the thymidine kinase (TK) locus. Mixture exposures gave dose–responses that differed from those for the individual chemicals; for the BaP-containing mixtures, an increased mutation frequency (MF) at low concentration combinations that were not mutagenic individually, and decreased MF at higher concentration combinations, compared to the calculated predicted additive MF of the individual chemicals. In contrast, the mixture of PhIP with GA did not increase MF above background levels. These data suggest BaP is driving the mutation response and that metabolic activation plays a role; in mixtures with BaP the increased/decreased MF above/below the expected additive MF the order is PhIP > AC > GA. The increase in MF at some low concentration combinations that include BaP is interesting and supports our previous work showing a similar response for BaP with PhIP, confirming this response is not limited to the BaP/PhIP combination. Moreover, the lack of a mutation response for PhIP with GA relative to the response of the individual chemicals at equivalent doses is interesting and may represent a potential avenue for reducing the risk of exposure to environmental carcinogens; specifically, removal of BaP from the mixture may reduce the mutation effect, although in the context of food this would be significantly challenging.</description><subject>Acrylamide</subject><subject>Background levels</subject><subject>Baseline studies</subject><subject>Benzo(a)pyrene</subject><subject>Binary mixtures</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Carcinogens</subject><subject>Chemical damage</subject><subject>Chemicals</subject><subject>Cooking</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA damage</subject><subject>Environmental Health</subject><subject>Exposure</subject><subject>Food</subject><subject>Genotoxic chemicals</subject><subject>Genotoxicity</subject><subject>High temperature</subject><subject>Impact damage</subject><subject>Metabolic activation</subject><subject>Metabolic rate</subject><subject>Mutagenicity</subject><subject>Mutation</subject><subject>Occupational health</subject><subject>Occupational Medicine/Industrial Medicine</subject><subject>Organic chemistry</subject><subject>Pharmacology/Toxicology</subject><subject>Pyrene</subject><subject>Pyridines</subject><subject>Regulatory Toxicology</subject><subject>Thymidine</subject><subject>Thymidine kinase</subject><issn>0340-5761</issn><issn>1432-0738</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp1kU2LFDEQhoMo7jj6A7xIwIuX1spHb5KjrK4KC172JtKkO9WzWaaTNknvOvtj_K1m6PUDwUMIVJ68VdRDyHMGrxmAepMBOMgGmG64YKaRD8iGScEbUEI_JBsQEppWnbIT8iTnawDGtRGPyYkA3hpQbEN-vIsZG4czBoeh0HwImHY-Fz9QG1w9xe5iWAvTUmzxMdCEeY4hY6ZxpL0PNh3o5L-XJa2lcoUUw41PMUw11e7pYNPgQ9xhoD2Gu_jFfp0PCQPSW1-u6Bijq1Mkf4PuLzY_JY9Gu8_47P7eksvz95dnH5uLzx8-nb29aAbJ2tIozUEN2oEQZjxtUVk7SqWM6DX2xva8BTCtZry3ozWjkuBaLW0rQTnshdiSV2vsnOK3BXPpJp8H3O9twLjkjjMmuAJWl7slL_9Br-OSQh3uSHHJjTK6UmylhhRzTjh2c_JTXVPHoDu661Z3XXXXHd11x-QX98lLP6H7_eOXrArwFcj1Keww_Wn9_9Sfg8CoHg</recordid><startdate>20181201</startdate><enddate>20181201</enddate><creator>David, Rhiannon M.</creator><creator>Gooderham, Nigel J.</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T2</scope><scope>7TK</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>MBDVC</scope><scope>PATMY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PYCSY</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20181201</creationdate><title>Dose-dependent synergistic and antagonistic mutation responses of binary mixtures of the environmental carcinogen benzo[a]pyrene with food-derived carcinogens</title><author>David, Rhiannon M. ; Gooderham, Nigel J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-78207c8d0339f65e7aaf47793b8eb9ab250095812bafa9f740d584a5407deb33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Acrylamide</topic><topic>Background levels</topic><topic>Baseline studies</topic><topic>Benzo(a)pyrene</topic><topic>Binary mixtures</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Carcinogens</topic><topic>Chemical damage</topic><topic>Chemicals</topic><topic>Cooking</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA damage</topic><topic>Environmental Health</topic><topic>Exposure</topic><topic>Food</topic><topic>Genotoxic chemicals</topic><topic>Genotoxicity</topic><topic>High temperature</topic><topic>Impact damage</topic><topic>Metabolic activation</topic><topic>Metabolic rate</topic><topic>Mutagenicity</topic><topic>Mutation</topic><topic>Occupational health</topic><topic>Occupational Medicine/Industrial Medicine</topic><topic>Organic chemistry</topic><topic>Pharmacology/Toxicology</topic><topic>Pyrene</topic><topic>Pyridines</topic><topic>Regulatory Toxicology</topic><topic>Thymidine</topic><topic>Thymidine kinase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>David, Rhiannon M.</creatorcontrib><creatorcontrib>Gooderham, Nigel J.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Research Library (Corporate)</collection><collection>Environmental Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Environmental Science Collection</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Archives of toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>David, Rhiannon M.</au><au>Gooderham, Nigel J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dose-dependent synergistic and antagonistic mutation responses of binary mixtures of the environmental carcinogen benzo[a]pyrene with food-derived carcinogens</atitle><jtitle>Archives of toxicology</jtitle><stitle>Arch Toxicol</stitle><addtitle>Arch Toxicol</addtitle><date>2018-12-01</date><risdate>2018</risdate><volume>92</volume><issue>12</issue><spage>3459</spage><epage>3469</epage><pages>3459-3469</pages><issn>0340-5761</issn><eissn>1432-0738</eissn><abstract>Cooking food at high temperatures produces genotoxic chemicals and there is concern about their impact on human health. DNA damage caused by individual chemicals has been investigated but few studies have examined the consequences of exposure to mixtures as found in food. The current study examined the mutagenic response to binary mixtures of benzo[a]pyrene (BaP) with glycidamide (GA), BaP with acrylamide (AC), or 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) with GA at human-relevant concentrations (sub-nM). The metabolically competent human MCL-5 cells were exposed to these chemicals individually or in mixtures and mutagenicity was assessed at the thymidine kinase (TK) locus. Mixture exposures gave dose–responses that differed from those for the individual chemicals; for the BaP-containing mixtures, an increased mutation frequency (MF) at low concentration combinations that were not mutagenic individually, and decreased MF at higher concentration combinations, compared to the calculated predicted additive MF of the individual chemicals. In contrast, the mixture of PhIP with GA did not increase MF above background levels. These data suggest BaP is driving the mutation response and that metabolic activation plays a role; in mixtures with BaP the increased/decreased MF above/below the expected additive MF the order is PhIP > AC > GA. The increase in MF at some low concentration combinations that include BaP is interesting and supports our previous work showing a similar response for BaP with PhIP, confirming this response is not limited to the BaP/PhIP combination. Moreover, the lack of a mutation response for PhIP with GA relative to the response of the individual chemicals at equivalent doses is interesting and may represent a potential avenue for reducing the risk of exposure to environmental carcinogens; specifically, removal of BaP from the mixture may reduce the mutation effect, although in the context of food this would be significantly challenging.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>30259071</pmid><doi>10.1007/s00204-018-2319-4</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acrylamide Background levels Baseline studies Benzo(a)pyrene Binary mixtures Biomedical and Life Sciences Biomedicine Carcinogens Chemical damage Chemicals Cooking Deoxyribonucleic acid DNA DNA damage Environmental Health Exposure Food Genotoxic chemicals Genotoxicity High temperature Impact damage Metabolic activation Metabolic rate Mutagenicity Mutation Occupational health Occupational Medicine/Industrial Medicine Organic chemistry Pharmacology/Toxicology Pyrene Pyridines Regulatory Toxicology Thymidine Thymidine kinase |
title | Dose-dependent synergistic and antagonistic mutation responses of binary mixtures of the environmental carcinogen benzo[a]pyrene with food-derived carcinogens |
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