Genetic polymorphisms of MPO, GSTT1, GSTM1, GSTP1, EPHX1 and NQO1 as risk factors of early‐onset lung cancer
Early‐onset lung cancer diagnosed up to the age of 50 is a very rare disease, with an increasing incidence rate. Differences in aetiology, characteristics and epidemiology of early and older onset lung cancer have been described previously, suggesting the importance of genetic factors in early‐onset...
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creator | Timofeeva, Maria Kropp, Silke Sauter, Wiebke Beckmann, Lars Rosenberger, Albert Illig, Thomas Jäger, Birgit Mittelstrass, Kirstin Dienemann, Hendrik Bartsch, Helmut Bickeböller, Heike Chang‐Claude, Jenny Risch, Angela Wichmann, Heinz‐Erich |
description | Early‐onset lung cancer diagnosed up to the age of 50 is a very rare disease, with an increasing incidence rate. Differences in aetiology, characteristics and epidemiology of early and older onset lung cancer have been described previously, suggesting the importance of genetic factors in early‐onset lung cancer aetiology. A case‐control study was conducted to investigate the effects of genetic polymorphisms in the MPO, EPHX1, GSTT1, GSTM1, GSTP1 and NQO1 genes on the risk of early‐onset lung cancer development. Six hundred thirty‐eight Caucasian patients under the age of 51 with confirmed primary lung cancer and 1,300 cancer free control individuals, matched by age and sex, were included in this analysis. Seventeen single nucleotide polymorphisms and two deletion polymorphisms were genotyped. No significant association was found for any of the analyzed polymorphisms and overall lung cancer risk. Nonsignificantly decreased risk of lung cancer was observed for carriers of 1 or 2 copies of GSTM1. Subgroup analysis revealed gender‐ and/or smoking‐specific effects of EPHX1 rs2854455 (IV‐1464C > T) and rs2234922 (His139Arg), GSTT1 deletion, GSTP1 rs1695 (Ile105Val), rs947895 (+991C > A) and rs4891 (Ser185Ser) and NQO1 rs1800566 (Pro187Ser) polymorphisms. However, none of the observed effects were confirmed by interaction tests nor were they significant after Bonferroni correction for multiple testing. In summary, our study suggested a modifying effect of polymorphisms in EPHX1, GSTP1, GSTT1, GSTM1 and NQO1 genes on the risk of early‐onset lung cancer. To confirm these observations and to eliminate possible bias in our analyses, larger studies are warranted. |
doi_str_mv | 10.1002/ijc.25175 |
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Differences in aetiology, characteristics and epidemiology of early and older onset lung cancer have been described previously, suggesting the importance of genetic factors in early‐onset lung cancer aetiology. A case‐control study was conducted to investigate the effects of genetic polymorphisms in the MPO, EPHX1, GSTT1, GSTM1, GSTP1 and NQO1 genes on the risk of early‐onset lung cancer development. Six hundred thirty‐eight Caucasian patients under the age of 51 with confirmed primary lung cancer and 1,300 cancer free control individuals, matched by age and sex, were included in this analysis. Seventeen single nucleotide polymorphisms and two deletion polymorphisms were genotyped. No significant association was found for any of the analyzed polymorphisms and overall lung cancer risk. Nonsignificantly decreased risk of lung cancer was observed for carriers of 1 or 2 copies of GSTM1. Subgroup analysis revealed gender‐ and/or smoking‐specific effects of EPHX1 rs2854455 (IV‐1464C > T) and rs2234922 (His139Arg), GSTT1 deletion, GSTP1 rs1695 (Ile105Val), rs947895 (+991C > A) and rs4891 (Ser185Ser) and NQO1 rs1800566 (Pro187Ser) polymorphisms. However, none of the observed effects were confirmed by interaction tests nor were they significant after Bonferroni correction for multiple testing. In summary, our study suggested a modifying effect of polymorphisms in EPHX1, GSTP1, GSTT1, GSTM1 and NQO1 genes on the risk of early‐onset lung cancer. To confirm these observations and to eliminate possible bias in our analyses, larger studies are warranted.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.25175</identifier><identifier>PMID: 20091863</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Age of Onset ; Carrier State ; detoxifying enzymes ; early onset ; Female ; genetic polymorphisms ; Genotype ; Glutathione S-Transferase pi - genetics ; Humans ; Introns ; lung cancer ; Lung Neoplasms - enzymology ; Lung Neoplasms - epidemiology ; Lung Neoplasms - genetics ; Male ; Middle Aged ; NAD(P)H Dehydrogenase (Quinone) - genetics ; Peroxidase - genetics ; Polymorphism, Genetic ; Polymorphism, Single Nucleotide ; Promoter Regions, Genetic ; Risk Factors ; Sequence Deletion ; Smoking - genetics</subject><ispartof>International journal of cancer, 2010-10, Vol.127 (7), p.1547-1561</ispartof><rights>Copyright © 2010 UICC</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3905-a76b42015b997b3578cb302d224deceb75e4009ea177e95dfae52952822a63d03</citedby><cites>FETCH-LOGICAL-c3905-a76b42015b997b3578cb302d224deceb75e4009ea177e95dfae52952822a63d03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fijc.25175$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fijc.25175$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20091863$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Timofeeva, Maria</creatorcontrib><creatorcontrib>Kropp, Silke</creatorcontrib><creatorcontrib>Sauter, Wiebke</creatorcontrib><creatorcontrib>Beckmann, Lars</creatorcontrib><creatorcontrib>Rosenberger, Albert</creatorcontrib><creatorcontrib>Illig, Thomas</creatorcontrib><creatorcontrib>Jäger, Birgit</creatorcontrib><creatorcontrib>Mittelstrass, Kirstin</creatorcontrib><creatorcontrib>Dienemann, Hendrik</creatorcontrib><creatorcontrib>Bartsch, Helmut</creatorcontrib><creatorcontrib>Bickeböller, Heike</creatorcontrib><creatorcontrib>Chang‐Claude, Jenny</creatorcontrib><creatorcontrib>Risch, Angela</creatorcontrib><creatorcontrib>Wichmann, Heinz‐Erich</creatorcontrib><creatorcontrib>LUCY-Consortium</creatorcontrib><creatorcontrib>The LUCY‐Consortium</creatorcontrib><title>Genetic polymorphisms of MPO, GSTT1, GSTM1, GSTP1, EPHX1 and NQO1 as risk factors of early‐onset lung cancer</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>Early‐onset lung cancer diagnosed up to the age of 50 is a very rare disease, with an increasing incidence rate. Differences in aetiology, characteristics and epidemiology of early and older onset lung cancer have been described previously, suggesting the importance of genetic factors in early‐onset lung cancer aetiology. A case‐control study was conducted to investigate the effects of genetic polymorphisms in the MPO, EPHX1, GSTT1, GSTM1, GSTP1 and NQO1 genes on the risk of early‐onset lung cancer development. Six hundred thirty‐eight Caucasian patients under the age of 51 with confirmed primary lung cancer and 1,300 cancer free control individuals, matched by age and sex, were included in this analysis. Seventeen single nucleotide polymorphisms and two deletion polymorphisms were genotyped. No significant association was found for any of the analyzed polymorphisms and overall lung cancer risk. Nonsignificantly decreased risk of lung cancer was observed for carriers of 1 or 2 copies of GSTM1. Subgroup analysis revealed gender‐ and/or smoking‐specific effects of EPHX1 rs2854455 (IV‐1464C > T) and rs2234922 (His139Arg), GSTT1 deletion, GSTP1 rs1695 (Ile105Val), rs947895 (+991C > A) and rs4891 (Ser185Ser) and NQO1 rs1800566 (Pro187Ser) polymorphisms. However, none of the observed effects were confirmed by interaction tests nor were they significant after Bonferroni correction for multiple testing. In summary, our study suggested a modifying effect of polymorphisms in EPHX1, GSTP1, GSTT1, GSTM1 and NQO1 genes on the risk of early‐onset lung cancer. To confirm these observations and to eliminate possible bias in our analyses, larger studies are warranted.</description><subject>Age of Onset</subject><subject>Carrier State</subject><subject>detoxifying enzymes</subject><subject>early onset</subject><subject>Female</subject><subject>genetic polymorphisms</subject><subject>Genotype</subject><subject>Glutathione S-Transferase pi - genetics</subject><subject>Humans</subject><subject>Introns</subject><subject>lung cancer</subject><subject>Lung Neoplasms - enzymology</subject><subject>Lung Neoplasms - epidemiology</subject><subject>Lung Neoplasms - genetics</subject><subject>Male</subject><subject>Middle Aged</subject><subject>NAD(P)H Dehydrogenase (Quinone) - genetics</subject><subject>Peroxidase - genetics</subject><subject>Polymorphism, Genetic</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Promoter Regions, Genetic</subject><subject>Risk Factors</subject><subject>Sequence Deletion</subject><subject>Smoking - genetics</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE1OwzAQRi0EoqWw4ALIO4REiu3EcbJEVWmLWlpEkdhFjjOBlPwUuxHKjiNwRk6CaQo7Vt9I8-aT5iF0SkmfEsKuspXqM04F30NdSkLhEEb5PuraHXEEdf0OOjJmRQilnHiHqMMICWngu11UjqCETabwusqbotLrl8wUBlcpni3ml3j0sFzSbczaWNgYLsZPFMsywXf3czsYrDPzilOpNpXe3oLUefP18VmVBjY4r8tnrGSpQB-jg1TmBk522UOPN8PlYOxM56PJ4HrqKDck3JHCjz1GKI_DUMQuF4GKXcISxrwEFMSCg2dfAEmFgJAnqQTOQs4CxqTvJsTtofO2d62rtxrMJioyoyDPZQlVbSLhBaFvcW7Ji5ZUujJGQxqtdVZI3USURD92I2s32tq17NmutY4LSP7IX50WuGqB9yyH5v-maHI7aCu_ATEHgLg</recordid><startdate>20101001</startdate><enddate>20101001</enddate><creator>Timofeeva, Maria</creator><creator>Kropp, Silke</creator><creator>Sauter, Wiebke</creator><creator>Beckmann, Lars</creator><creator>Rosenberger, Albert</creator><creator>Illig, Thomas</creator><creator>Jäger, Birgit</creator><creator>Mittelstrass, Kirstin</creator><creator>Dienemann, Hendrik</creator><creator>Bartsch, Helmut</creator><creator>Bickeböller, Heike</creator><creator>Chang‐Claude, Jenny</creator><creator>Risch, Angela</creator><creator>Wichmann, Heinz‐Erich</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><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>7X8</scope></search><sort><creationdate>20101001</creationdate><title>Genetic polymorphisms of MPO, GSTT1, GSTM1, GSTP1, EPHX1 and NQO1 as risk factors of early‐onset lung cancer</title><author>Timofeeva, Maria ; Kropp, Silke ; Sauter, Wiebke ; Beckmann, Lars ; Rosenberger, Albert ; Illig, Thomas ; Jäger, Birgit ; Mittelstrass, Kirstin ; Dienemann, Hendrik ; Bartsch, Helmut ; Bickeböller, Heike ; Chang‐Claude, Jenny ; Risch, Angela ; Wichmann, Heinz‐Erich</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3905-a76b42015b997b3578cb302d224deceb75e4009ea177e95dfae52952822a63d03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Age of Onset</topic><topic>Carrier State</topic><topic>detoxifying enzymes</topic><topic>early onset</topic><topic>Female</topic><topic>genetic polymorphisms</topic><topic>Genotype</topic><topic>Glutathione S-Transferase pi - genetics</topic><topic>Humans</topic><topic>Introns</topic><topic>lung cancer</topic><topic>Lung Neoplasms - enzymology</topic><topic>Lung Neoplasms - epidemiology</topic><topic>Lung Neoplasms - genetics</topic><topic>Male</topic><topic>Middle Aged</topic><topic>NAD(P)H Dehydrogenase (Quinone) - genetics</topic><topic>Peroxidase - genetics</topic><topic>Polymorphism, Genetic</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Promoter Regions, Genetic</topic><topic>Risk Factors</topic><topic>Sequence Deletion</topic><topic>Smoking - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Timofeeva, Maria</creatorcontrib><creatorcontrib>Kropp, Silke</creatorcontrib><creatorcontrib>Sauter, Wiebke</creatorcontrib><creatorcontrib>Beckmann, Lars</creatorcontrib><creatorcontrib>Rosenberger, Albert</creatorcontrib><creatorcontrib>Illig, Thomas</creatorcontrib><creatorcontrib>Jäger, Birgit</creatorcontrib><creatorcontrib>Mittelstrass, Kirstin</creatorcontrib><creatorcontrib>Dienemann, Hendrik</creatorcontrib><creatorcontrib>Bartsch, Helmut</creatorcontrib><creatorcontrib>Bickeböller, Heike</creatorcontrib><creatorcontrib>Chang‐Claude, Jenny</creatorcontrib><creatorcontrib>Risch, Angela</creatorcontrib><creatorcontrib>Wichmann, Heinz‐Erich</creatorcontrib><creatorcontrib>LUCY-Consortium</creatorcontrib><creatorcontrib>The LUCY‐Consortium</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Timofeeva, Maria</au><au>Kropp, Silke</au><au>Sauter, Wiebke</au><au>Beckmann, Lars</au><au>Rosenberger, Albert</au><au>Illig, Thomas</au><au>Jäger, Birgit</au><au>Mittelstrass, Kirstin</au><au>Dienemann, Hendrik</au><au>Bartsch, Helmut</au><au>Bickeböller, Heike</au><au>Chang‐Claude, Jenny</au><au>Risch, Angela</au><au>Wichmann, Heinz‐Erich</au><aucorp>LUCY-Consortium</aucorp><aucorp>The LUCY‐Consortium</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic polymorphisms of MPO, GSTT1, GSTM1, GSTP1, EPHX1 and NQO1 as risk factors of early‐onset lung cancer</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>2010-10-01</date><risdate>2010</risdate><volume>127</volume><issue>7</issue><spage>1547</spage><epage>1561</epage><pages>1547-1561</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><abstract>Early‐onset lung cancer diagnosed up to the age of 50 is a very rare disease, with an increasing incidence rate. Differences in aetiology, characteristics and epidemiology of early and older onset lung cancer have been described previously, suggesting the importance of genetic factors in early‐onset lung cancer aetiology. A case‐control study was conducted to investigate the effects of genetic polymorphisms in the MPO, EPHX1, GSTT1, GSTM1, GSTP1 and NQO1 genes on the risk of early‐onset lung cancer development. Six hundred thirty‐eight Caucasian patients under the age of 51 with confirmed primary lung cancer and 1,300 cancer free control individuals, matched by age and sex, were included in this analysis. Seventeen single nucleotide polymorphisms and two deletion polymorphisms were genotyped. No significant association was found for any of the analyzed polymorphisms and overall lung cancer risk. Nonsignificantly decreased risk of lung cancer was observed for carriers of 1 or 2 copies of GSTM1. Subgroup analysis revealed gender‐ and/or smoking‐specific effects of EPHX1 rs2854455 (IV‐1464C > T) and rs2234922 (His139Arg), GSTT1 deletion, GSTP1 rs1695 (Ile105Val), rs947895 (+991C > A) and rs4891 (Ser185Ser) and NQO1 rs1800566 (Pro187Ser) polymorphisms. However, none of the observed effects were confirmed by interaction tests nor were they significant after Bonferroni correction for multiple testing. In summary, our study suggested a modifying effect of polymorphisms in EPHX1, GSTP1, GSTT1, GSTM1 and NQO1 genes on the risk of early‐onset lung cancer. To confirm these observations and to eliminate possible bias in our analyses, larger studies are warranted.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>20091863</pmid><doi>10.1002/ijc.25175</doi><tpages>15</tpages></addata></record> |
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subjects | Age of Onset Carrier State detoxifying enzymes early onset Female genetic polymorphisms Genotype Glutathione S-Transferase pi - genetics Humans Introns lung cancer Lung Neoplasms - enzymology Lung Neoplasms - epidemiology Lung Neoplasms - genetics Male Middle Aged NAD(P)H Dehydrogenase (Quinone) - genetics Peroxidase - genetics Polymorphism, Genetic Polymorphism, Single Nucleotide Promoter Regions, Genetic Risk Factors Sequence Deletion Smoking - genetics |
title | Genetic polymorphisms of MPO, GSTT1, GSTM1, GSTP1, EPHX1 and NQO1 as risk factors of early‐onset lung cancer |
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