Polycyclic aromatic hydrocarbons in cigarette sidestream smoke particulates from a Taiwanese brand and their carcinogenic relevance
Polycyclic aromatic hydrocarbons (PAHs) adsorbed on cigarette sidestream smoke particulates (CSSPs) have been regarded as important contributors to lung carcinogenesis in never smokers. However, limited information is available on PAH levels in cigarette sidestream smoke. Here we determine the conce...
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Veröffentlicht in: | Chemosphere (Oxford) 2011, Vol.82 (3), p.477-482 |
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description | Polycyclic aromatic hydrocarbons (PAHs) adsorbed on cigarette sidestream smoke particulates (CSSPs) have been regarded as important contributors to lung carcinogenesis in never smokers. However, limited information is available on PAH levels in cigarette sidestream smoke. Here we determine the concentrations of 22 PAHs, including 16 US EPA priority PAHs, in CSSPs generated from a high market-share domestic brand in Taiwan. Five of the 22 PAHs are undetectable. The remaining 17 PAHs constitute about 0.022% of the total mass of CSSPs. Near one fifth of the PAH mass come from IARC group 1 and group 2 carcinogens. Carcinogenic potency is equivalent to 144
ng benzo[
a]pyrene per cigarette converted according to potency equivalency factors (PEFs). The CSSP condensate could activate AhR activity and induce AhR target gene expression. High concentrations of CSSPs also exhibited AhR-independent cytotoxicity. However, mixing the 17 PAHs as the composition in the CSSP condensate could not reconstitute either capacity. Since AhR activation and cytotoxicity are important mechanisms underlying carcinogenic potency, the results suggest that other component compounds play a more active role in carcinogenesis. The approach of individual PAH profiling plus PEF conversion commonly used in risk assessment is likely to underestimate the risk caused by environmental cigarette smoke exposure. |
doi_str_mv | 10.1016/j.chemosphere.2010.09.045 |
format | Article |
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ng benzo[
a]pyrene per cigarette converted according to potency equivalency factors (PEFs). The CSSP condensate could activate AhR activity and induce AhR target gene expression. High concentrations of CSSPs also exhibited AhR-independent cytotoxicity. However, mixing the 17 PAHs as the composition in the CSSP condensate could not reconstitute either capacity. Since AhR activation and cytotoxicity are important mechanisms underlying carcinogenic potency, the results suggest that other component compounds play a more active role in carcinogenesis. The approach of individual PAH profiling plus PEF conversion commonly used in risk assessment is likely to underestimate the risk caused by environmental cigarette smoke exposure.</description><identifier>ISSN: 0045-6535</identifier><identifier>EISSN: 1879-1298</identifier><identifier>DOI: 10.1016/j.chemosphere.2010.09.045</identifier><identifier>PMID: 20947129</identifier><identifier>CODEN: CMSHAF</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Activation ; AhR ; Biological and medical sciences ; Carcinogens ; Carcinogens - analysis ; Carcinogens - toxicity ; Cell Survival - drug effects ; Cigarette sidestream smoke particulates ; Cigarettes ; Condensates ; Cytotoxicity ; Equivalence ; Lung cancer ; Medical sciences ; PAH ; Particulates ; Polyallylamine hydrochloride ; Polycyclic aromatic hydrocarbons ; Polycyclic Aromatic Hydrocarbons - analysis ; Polycyclic Aromatic Hydrocarbons - toxicity ; Receptors, Aryl Hydrocarbon - metabolism ; Smoke ; Smoke - analysis ; Taiwan ; Tobacco Smoke Pollution - analysis ; Tobacco, tobacco smoking ; Toxicology</subject><ispartof>Chemosphere (Oxford), 2011, Vol.82 (3), p.477-482</ispartof><rights>2010 Elsevier Ltd</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2010 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c471t-cab423f65a0ecb682ea5fc10de12d6e6fb16e0e0472946700e3cec5d0cb135003</citedby><cites>FETCH-LOGICAL-c471t-cab423f65a0ecb682ea5fc10de12d6e6fb16e0e0472946700e3cec5d0cb135003</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S004565351001060X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,4010,27900,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23703884$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20947129$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Hui-Ling</creatorcontrib><creatorcontrib>Hsieh, Dennis P.H.</creatorcontrib><creatorcontrib>Li, Lih-Ann</creatorcontrib><title>Polycyclic aromatic hydrocarbons in cigarette sidestream smoke particulates from a Taiwanese brand and their carcinogenic relevance</title><title>Chemosphere (Oxford)</title><addtitle>Chemosphere</addtitle><description>Polycyclic aromatic hydrocarbons (PAHs) adsorbed on cigarette sidestream smoke particulates (CSSPs) have been regarded as important contributors to lung carcinogenesis in never smokers. However, limited information is available on PAH levels in cigarette sidestream smoke. Here we determine the concentrations of 22 PAHs, including 16 US EPA priority PAHs, in CSSPs generated from a high market-share domestic brand in Taiwan. Five of the 22 PAHs are undetectable. The remaining 17 PAHs constitute about 0.022% of the total mass of CSSPs. Near one fifth of the PAH mass come from IARC group 1 and group 2 carcinogens. Carcinogenic potency is equivalent to 144
ng benzo[
a]pyrene per cigarette converted according to potency equivalency factors (PEFs). The CSSP condensate could activate AhR activity and induce AhR target gene expression. High concentrations of CSSPs also exhibited AhR-independent cytotoxicity. However, mixing the 17 PAHs as the composition in the CSSP condensate could not reconstitute either capacity. Since AhR activation and cytotoxicity are important mechanisms underlying carcinogenic potency, the results suggest that other component compounds play a more active role in carcinogenesis. The approach of individual PAH profiling plus PEF conversion commonly used in risk assessment is likely to underestimate the risk caused by environmental cigarette smoke exposure.</description><subject>Activation</subject><subject>AhR</subject><subject>Biological and medical sciences</subject><subject>Carcinogens</subject><subject>Carcinogens - analysis</subject><subject>Carcinogens - toxicity</subject><subject>Cell Survival - drug effects</subject><subject>Cigarette sidestream smoke particulates</subject><subject>Cigarettes</subject><subject>Condensates</subject><subject>Cytotoxicity</subject><subject>Equivalence</subject><subject>Lung cancer</subject><subject>Medical sciences</subject><subject>PAH</subject><subject>Particulates</subject><subject>Polyallylamine hydrochloride</subject><subject>Polycyclic aromatic hydrocarbons</subject><subject>Polycyclic Aromatic Hydrocarbons - analysis</subject><subject>Polycyclic Aromatic Hydrocarbons - toxicity</subject><subject>Receptors, Aryl Hydrocarbon - metabolism</subject><subject>Smoke</subject><subject>Smoke - analysis</subject><subject>Taiwan</subject><subject>Tobacco Smoke Pollution - analysis</subject><subject>Tobacco, tobacco smoking</subject><subject>Toxicology</subject><issn>0045-6535</issn><issn>1879-1298</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU2P0zAQhi0EYrsLfwGZA4JLyzixk_iIquVDWgkOy9lyJpOtSxIXO91Vz_xxpmr5OCEOlq3R886M31eIlwpWClT1drvCDY0x7zaUaFUA18GuQJtHYqGa2i5VYZvHYgFcWlamNBfiMuctAIuNfSouCrC6ZmghfnyJwwEPOASUPsXRz_zYHLoU0ac2TlmGSWK484nmmWQOHeU5kR9lHuM3kjufWLEf_ExZ9txAennrw4OfKJNsk586eTzzhkKS3BPDFO9o4imJBrr3E9Iz8aT3Q6bn5_tKfH1_fbv-uLz5_OHT-t3NEnnZeYm-1UXZV8YDYVs1BXnTo4KOVNFVVPWtqggIdF1YXdUAVCKh6QBbVRqA8kq8PvXdpfh9z_9wY8hIw8DLxn12jSl1Y6wtmHzzT1JVtdJWG10zak8opphzot7tUhh9OjgF7piW27q_0nLHtBxYx9Gw9sV5zL4dqfut_BUPA6_OgM_oh57txJD_cGUNZdNo5tYnjti--0DJZQzE1nYhEc6ui-E_1vkJqnS8cQ</recordid><startdate>2011</startdate><enddate>2011</enddate><creator>Lee, Hui-Ling</creator><creator>Hsieh, Dennis P.H.</creator><creator>Li, Lih-Ann</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</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>8FD</scope><scope>FR3</scope><scope>KR7</scope><scope>7ST</scope><scope>7U1</scope><scope>7U2</scope><scope>7U7</scope><scope>C1K</scope><scope>SOI</scope></search><sort><creationdate>2011</creationdate><title>Polycyclic aromatic hydrocarbons in cigarette sidestream smoke particulates from a Taiwanese brand and their carcinogenic relevance</title><author>Lee, Hui-Ling ; Hsieh, Dennis P.H. ; Li, Lih-Ann</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c471t-cab423f65a0ecb682ea5fc10de12d6e6fb16e0e0472946700e3cec5d0cb135003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Activation</topic><topic>AhR</topic><topic>Biological and medical sciences</topic><topic>Carcinogens</topic><topic>Carcinogens - analysis</topic><topic>Carcinogens - toxicity</topic><topic>Cell Survival - drug effects</topic><topic>Cigarette sidestream smoke particulates</topic><topic>Cigarettes</topic><topic>Condensates</topic><topic>Cytotoxicity</topic><topic>Equivalence</topic><topic>Lung cancer</topic><topic>Medical sciences</topic><topic>PAH</topic><topic>Particulates</topic><topic>Polyallylamine hydrochloride</topic><topic>Polycyclic aromatic hydrocarbons</topic><topic>Polycyclic Aromatic Hydrocarbons - analysis</topic><topic>Polycyclic Aromatic Hydrocarbons - toxicity</topic><topic>Receptors, Aryl Hydrocarbon - metabolism</topic><topic>Smoke</topic><topic>Smoke - analysis</topic><topic>Taiwan</topic><topic>Tobacco Smoke Pollution - analysis</topic><topic>Tobacco, tobacco smoking</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Hui-Ling</creatorcontrib><creatorcontrib>Hsieh, Dennis P.H.</creatorcontrib><creatorcontrib>Li, Lih-Ann</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Civil Engineering Abstracts</collection><collection>Environment Abstracts</collection><collection>Risk Abstracts</collection><collection>Safety Science and Risk</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><jtitle>Chemosphere (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Hui-Ling</au><au>Hsieh, Dennis P.H.</au><au>Li, Lih-Ann</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polycyclic aromatic hydrocarbons in cigarette sidestream smoke particulates from a Taiwanese brand and their carcinogenic relevance</atitle><jtitle>Chemosphere (Oxford)</jtitle><addtitle>Chemosphere</addtitle><date>2011</date><risdate>2011</risdate><volume>82</volume><issue>3</issue><spage>477</spage><epage>482</epage><pages>477-482</pages><issn>0045-6535</issn><eissn>1879-1298</eissn><coden>CMSHAF</coden><abstract>Polycyclic aromatic hydrocarbons (PAHs) adsorbed on cigarette sidestream smoke particulates (CSSPs) have been regarded as important contributors to lung carcinogenesis in never smokers. However, limited information is available on PAH levels in cigarette sidestream smoke. Here we determine the concentrations of 22 PAHs, including 16 US EPA priority PAHs, in CSSPs generated from a high market-share domestic brand in Taiwan. Five of the 22 PAHs are undetectable. The remaining 17 PAHs constitute about 0.022% of the total mass of CSSPs. Near one fifth of the PAH mass come from IARC group 1 and group 2 carcinogens. Carcinogenic potency is equivalent to 144
ng benzo[
a]pyrene per cigarette converted according to potency equivalency factors (PEFs). The CSSP condensate could activate AhR activity and induce AhR target gene expression. High concentrations of CSSPs also exhibited AhR-independent cytotoxicity. However, mixing the 17 PAHs as the composition in the CSSP condensate could not reconstitute either capacity. Since AhR activation and cytotoxicity are important mechanisms underlying carcinogenic potency, the results suggest that other component compounds play a more active role in carcinogenesis. The approach of individual PAH profiling plus PEF conversion commonly used in risk assessment is likely to underestimate the risk caused by environmental cigarette smoke exposure.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>20947129</pmid><doi>10.1016/j.chemosphere.2010.09.045</doi><tpages>6</tpages></addata></record> |
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subjects | Activation AhR Biological and medical sciences Carcinogens Carcinogens - analysis Carcinogens - toxicity Cell Survival - drug effects Cigarette sidestream smoke particulates Cigarettes Condensates Cytotoxicity Equivalence Lung cancer Medical sciences PAH Particulates Polyallylamine hydrochloride Polycyclic aromatic hydrocarbons Polycyclic Aromatic Hydrocarbons - analysis Polycyclic Aromatic Hydrocarbons - toxicity Receptors, Aryl Hydrocarbon - metabolism Smoke Smoke - analysis Taiwan Tobacco Smoke Pollution - analysis Tobacco, tobacco smoking Toxicology |
title | Polycyclic aromatic hydrocarbons in cigarette sidestream smoke particulates from a Taiwanese brand and their carcinogenic relevance |
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