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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Veröffentlicht in:International journal of cancer 2010-10, Vol.127 (7), p.1547-1561
Hauptverfasser: 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
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container_issue 7
container_start_page 1547
container_title International journal of cancer
container_volume 127
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 &gt; T) and rs2234922 (His139Arg), GSTT1 deletion, GSTP1 rs1695 (Ile105Val), rs947895 (+991C &gt; 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. 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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 &gt; T) and rs2234922 (His139Arg), GSTT1 deletion, GSTP1 rs1695 (Ile105Val), rs947895 (+991C &gt; 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. 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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 &gt; T) and rs2234922 (His139Arg), GSTT1 deletion, GSTP1 rs1695 (Ile105Val), rs947895 (+991C &gt; 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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