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Cytochrome P450 1A1 exon 7 polymorphism and susceptibility to lung cancer in the Chinese population: an updated meta-analysis and review

BACKGROUND: Although many epidemiologic studies have investigated the cytochrome P450 1A1 (CYP1A1) exon 7 gene polymorphism and its association with lung cancer (LC), definitive conclusions cannot be drawn. OBJECTIVE: To clarify the effects of CYP1A1 exon 7 polymorphism on the risk of LC, an updated...

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Autores principales: Wei, Xiu-ping, Hu, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4494617/
https://www.ncbi.nlm.nih.gov/pubmed/26170697
http://dx.doi.org/10.2147/OTT.S84575
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author Wei, Xiu-ping
Hu, Jie
author_facet Wei, Xiu-ping
Hu, Jie
author_sort Wei, Xiu-ping
collection PubMed
description BACKGROUND: Although many epidemiologic studies have investigated the cytochrome P450 1A1 (CYP1A1) exon 7 gene polymorphism and its association with lung cancer (LC), definitive conclusions cannot be drawn. OBJECTIVE: To clarify the effects of CYP1A1 exon 7 polymorphism on the risk of LC, an updated meta-analysis was performed in the Chinese population. METHODS: Related studies were identified from PubMed, Springer Link, Ovid, the Chinese Wanfang Data Knowledge Service Platform, Chinese National Knowledge Infrastructure (CNKI), and the Chinese Biology Medicine (CBM) databases until October 2014. Odds ratios (ORs) with 95% confidence intervals (CIs) were used to assess the strength of the associations. RESULTS: A total of 25 articles including 3,540 LC cases and 5,284 controls were included in this meta-analysis. Overall, significant association was found between CYP1A1 exon 7 polymorphism and LC risk when all studies in the Chinese population were pooled into this meta-analysis (GG versus AA: OR = 1.71, 95% CI: 1.46–2.01; GG versus AG: OR = 1.41, 95% CI: 1.21–1.64; GG + AG versus AA: OR = 1.37, 95% CI: 1.16–1.62; GG versus AA + AG: OR = 1.52, 95% CI: 1.32–1.76). In subgroup analyses stratified by ethnicity, source of controls, and geographical locations, significantly increased risk was found in Chinese Han people, in population-based studies, in hospital-based studies, in South China, and in North China. CONCLUSION: This meta-analysis provides the evidence that CYP1A1 exon 7 polymorphism may contribute to LC development in the Chinese population, and studies with a larger sample size and wider population spectrum are warranted to verify this finding.
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spelling pubmed-44946172015-07-13 Cytochrome P450 1A1 exon 7 polymorphism and susceptibility to lung cancer in the Chinese population: an updated meta-analysis and review Wei, Xiu-ping Hu, Jie Onco Targets Ther Original Research BACKGROUND: Although many epidemiologic studies have investigated the cytochrome P450 1A1 (CYP1A1) exon 7 gene polymorphism and its association with lung cancer (LC), definitive conclusions cannot be drawn. OBJECTIVE: To clarify the effects of CYP1A1 exon 7 polymorphism on the risk of LC, an updated meta-analysis was performed in the Chinese population. METHODS: Related studies were identified from PubMed, Springer Link, Ovid, the Chinese Wanfang Data Knowledge Service Platform, Chinese National Knowledge Infrastructure (CNKI), and the Chinese Biology Medicine (CBM) databases until October 2014. Odds ratios (ORs) with 95% confidence intervals (CIs) were used to assess the strength of the associations. RESULTS: A total of 25 articles including 3,540 LC cases and 5,284 controls were included in this meta-analysis. Overall, significant association was found between CYP1A1 exon 7 polymorphism and LC risk when all studies in the Chinese population were pooled into this meta-analysis (GG versus AA: OR = 1.71, 95% CI: 1.46–2.01; GG versus AG: OR = 1.41, 95% CI: 1.21–1.64; GG + AG versus AA: OR = 1.37, 95% CI: 1.16–1.62; GG versus AA + AG: OR = 1.52, 95% CI: 1.32–1.76). In subgroup analyses stratified by ethnicity, source of controls, and geographical locations, significantly increased risk was found in Chinese Han people, in population-based studies, in hospital-based studies, in South China, and in North China. CONCLUSION: This meta-analysis provides the evidence that CYP1A1 exon 7 polymorphism may contribute to LC development in the Chinese population, and studies with a larger sample size and wider population spectrum are warranted to verify this finding. Dove Medical Press 2015-07-02 /pmc/articles/PMC4494617/ /pubmed/26170697 http://dx.doi.org/10.2147/OTT.S84575 Text en © 2015 Wei and Hu. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Wei, Xiu-ping
Hu, Jie
Cytochrome P450 1A1 exon 7 polymorphism and susceptibility to lung cancer in the Chinese population: an updated meta-analysis and review
title Cytochrome P450 1A1 exon 7 polymorphism and susceptibility to lung cancer in the Chinese population: an updated meta-analysis and review
title_full Cytochrome P450 1A1 exon 7 polymorphism and susceptibility to lung cancer in the Chinese population: an updated meta-analysis and review
title_fullStr Cytochrome P450 1A1 exon 7 polymorphism and susceptibility to lung cancer in the Chinese population: an updated meta-analysis and review
title_full_unstemmed Cytochrome P450 1A1 exon 7 polymorphism and susceptibility to lung cancer in the Chinese population: an updated meta-analysis and review
title_short Cytochrome P450 1A1 exon 7 polymorphism and susceptibility to lung cancer in the Chinese population: an updated meta-analysis and review
title_sort cytochrome p450 1a1 exon 7 polymorphism and susceptibility to lung cancer in the chinese population: an updated meta-analysis and review
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4494617/
https://www.ncbi.nlm.nih.gov/pubmed/26170697
http://dx.doi.org/10.2147/OTT.S84575
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