Please use this identifier to cite or link to this item: https://doi.org/10.1158/1055-9965.EPI-07-2786
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dc.titleCYP1A1, GSTM1, and GSTT1 polymorphisms, smoking, and lung cancer risk in a pooled analysis among Asian populations
dc.contributor.authorLee, K.-M.
dc.contributor.authorKang, D.
dc.contributor.authorClapper, M.L.
dc.contributor.authorIngelman-Sundberg, M.
dc.contributor.authorOno-Kihara, M.
dc.contributor.authorKiyohara, C.
dc.contributor.authorMin, S.
dc.contributor.authorLan, Q.
dc.contributor.authorLe Marchand, L.
dc.contributor.authorLin, P.
dc.contributor.authorLi Lung, M.
dc.contributor.authorPinarbasi, H.
dc.contributor.authorPisani, P.
dc.contributor.authorSrivatanakul, P.
dc.contributor.authorSeow, A.
dc.contributor.authorSugimura, H.
dc.contributor.authorTokudome, S.
dc.contributor.authorYokota, J.
dc.contributor.authorTaioli, E.
dc.date.accessioned2014-11-26T07:43:58Z
dc.date.available2014-11-26T07:43:58Z
dc.date.issued2008-05
dc.identifier.citationLee, K.-M., Kang, D., Clapper, M.L., Ingelman-Sundberg, M., Ono-Kihara, M., Kiyohara, C., Min, S., Lan, Q., Le Marchand, L., Lin, P., Li Lung, M., Pinarbasi, H., Pisani, P., Srivatanakul, P., Seow, A., Sugimura, H., Tokudome, S., Yokota, J., Taioli, E. (2008-05). CYP1A1, GSTM1, and GSTT1 polymorphisms, smoking, and lung cancer risk in a pooled analysis among Asian populations. Cancer Epidemiology Biomarkers and Prevention 17 (5) : 1120-1126. ScholarBank@NUS Repository. https://doi.org/10.1158/1055-9965.EPI-07-2786
dc.identifier.issn10559965
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/109280
dc.description.abstractTo evaluate the roles of CYP1A1 polymorphisms [Ile462Val and T6235C (MspI)] and deletion of GSTM1 and and GSTT1 in lung cancer development in Asian populations, a pooled analysis was conducted on 13 existing studies included in Genetic Susceptibility to Environmental Carcinogenesis database. This pooled analysis included 1,971 cases and 2,130 controls. Lung cancer riskwas estimated as odds ratios (OR) and 95% confidence intervals (95% CI) using unconditional logistic regression model adjusting for age, sex, and pack-year. The CYP1A1 6235C variant was associated with squamous cell lung cancer (TC versus TT: OR, 1.42; 95% CI, 0.96-2.09; CC versus TT: OR, 1.97; 95% CI, 1.26-3.07; Ptrend = 0.003). In haplotype analysis, 462Val-6235T and Ile-C haplotypes were associated with lung cancer risk with reference to the Ile-T haplotype (OR, 3.41; 95% CI, 1.78-6.53 and OR, 1.39; 95% CI, 1.12-1.71, respectively). The GSTM1-null genotype increased squamous cell lung cancer risk(OR, 1.36; 95% CI, 1.05-1.77). When the interaction was evaluated with smoking, increasing trend of lung cancer riskas pack-year increased was stronger among those with the CYP1A1 6235 TC/CC genotype compared with those with TT genotype (Pinteraction = 0.001) and with the GSTM1-null genotype compared with the present type (P interaction = 0.08, when no genotype effect with no exposure was assumed). These results suggest that genetic polymorphisms in CYP1A1 and GSTM1 are associated with lung cancer riskin Asian populations. However, further investigation is warranted considering the relatively small sample size when subgroup analyses were done and the lack of environmental exposure data other than smoking. Copyright © 2008 American Association for Cancer Research.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1158/1055-9965.EPI-07-2786
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCOMMUNITY,OCCUPATIONAL & FAMILY MEDICINE
dc.description.doi10.1158/1055-9965.EPI-07-2786
dc.description.sourcetitleCancer Epidemiology Biomarkers and Prevention
dc.description.volume17
dc.description.issue5
dc.description.page1120-1126
dc.description.codenCEBPE
dc.identifier.isiut000256012800016
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