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- Publisher Website: 10.1158/1055-9965.EPI-07-2786
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- PMID: 18463401
- WOS: WOS:000256012800016
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Article: CYP1A1, GSTM1, and GSTT1 polymorphisms, smoking, and lung cancer risk in a pooled analysis among Asian populations
Title | CYP1A1, GSTM1, and GSTT1 polymorphisms, smoking, and lung cancer risk in a pooled analysis among Asian populations |
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Authors | |
Issue Date | 2008 |
Citation | Cancer Epidemiology Biomarkers And Prevention, 2008, v. 17 n. 5, p. 1120-1126 How to Cite? |
Abstract | To evaluate the roles of CYP1A1 polymorphisms [Ile 462Val and T 6235C (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; P trend = 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 (P interaction = 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. |
Persistent Identifier | http://hdl.handle.net/10722/150824 |
ISSN | 2023 Impact Factor: 3.7 2023 SCImago Journal Rankings: 1.688 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Lee, KM | en_US |
dc.contributor.author | Kang, D | en_US |
dc.contributor.author | Clapper, ML | en_US |
dc.contributor.author | IngelmanSundberg, M | en_US |
dc.contributor.author | OnoKihara, M | en_US |
dc.contributor.author | Kiyohara, C | en_US |
dc.contributor.author | Min, S | en_US |
dc.contributor.author | Lan, Q | en_US |
dc.contributor.author | Le Marchand, L | en_US |
dc.contributor.author | Lin, P | en_US |
dc.contributor.author | Li Lung, M | en_US |
dc.contributor.author | Pinarbasi, H | en_US |
dc.contributor.author | Pisani, P | en_US |
dc.contributor.author | Srivatanakul, P | en_US |
dc.contributor.author | Seow, A | en_US |
dc.contributor.author | Sugimura, H | en_US |
dc.contributor.author | Tokudome, S | en_US |
dc.contributor.author | Yokota, J | en_US |
dc.contributor.author | Taioli, E | en_US |
dc.date.accessioned | 2012-06-26T06:11:32Z | - |
dc.date.available | 2012-06-26T06:11:32Z | - |
dc.date.issued | 2008 | en_US |
dc.identifier.citation | Cancer Epidemiology Biomarkers And Prevention, 2008, v. 17 n. 5, p. 1120-1126 | en_US |
dc.identifier.issn | 1055-9965 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/150824 | - |
dc.description.abstract | To evaluate the roles of CYP1A1 polymorphisms [Ile 462Val and T 6235C (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; P trend = 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 (P interaction = 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. | en_US |
dc.language | eng | en_US |
dc.relation.ispartof | Cancer Epidemiology Biomarkers and Prevention | en_US |
dc.title | CYP1A1, GSTM1, and GSTT1 polymorphisms, smoking, and lung cancer risk in a pooled analysis among Asian populations | en_US |
dc.type | Article | en_US |
dc.identifier.email | Li Lung, M:mlilung@hku.hk | en_US |
dc.identifier.authority | Li Lung, M=rp00300 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1158/1055-9965.EPI-07-2786 | en_US |
dc.identifier.pmid | 18463401 | - |
dc.identifier.scopus | eid_2-s2.0-52649148138 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-52649148138&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 17 | en_US |
dc.identifier.issue | 5 | en_US |
dc.identifier.spage | 1120 | en_US |
dc.identifier.epage | 1126 | en_US |
dc.identifier.isi | WOS:000256012800016 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Lee, KM=26642943400 | en_US |
dc.identifier.scopusauthorid | Kang, D=7402889335 | en_US |
dc.identifier.scopusauthorid | Clapper, ML=7005163671 | en_US |
dc.identifier.scopusauthorid | IngelmanSundberg, M=7101739504 | en_US |
dc.identifier.scopusauthorid | OnoKihara, M=25223715500 | en_US |
dc.identifier.scopusauthorid | Kiyohara, C=7005966447 | en_US |
dc.identifier.scopusauthorid | Min, S=25223796000 | en_US |
dc.identifier.scopusauthorid | Lan, Q=23970641100 | en_US |
dc.identifier.scopusauthorid | Le Marchand, L=7006229986 | en_US |
dc.identifier.scopusauthorid | Lin, P=8960773100 | en_US |
dc.identifier.scopusauthorid | Li Lung, M=7006411788 | en_US |
dc.identifier.scopusauthorid | Pinarbasi, H=6602428486 | en_US |
dc.identifier.scopusauthorid | Pisani, P=7006949543 | en_US |
dc.identifier.scopusauthorid | Srivatanakul, P=6701499809 | en_US |
dc.identifier.scopusauthorid | Seow, A=7004099964 | en_US |
dc.identifier.scopusauthorid | Sugimura, H=7103031997 | en_US |
dc.identifier.scopusauthorid | Tokudome, S=7006179933 | en_US |
dc.identifier.scopusauthorid | Yokota, J=7102553031 | en_US |
dc.identifier.scopusauthorid | Taioli, E=7005607233 | en_US |
dc.identifier.citeulike | 5143414 | - |
dc.identifier.issnl | 1055-9965 | - |