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Meta-Analysis of Cytochrome P-450 2C9 Polymorphism and Colorectal Cancer Risk

BACKGROUND: CYP2C9 encodes a member of the cytochrome P450 superfamily of enzymes which play a central role in activating and detoxifying many carcinogens and endogenous compounds thought to be involved in the development of colorectal cancer (CRC). In the past decade, the relationship between CYP2C...

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Detalles Bibliográficos
Autores principales: Liang, Shuo, Hu, Jingsong, Cao, Weijun, Cai, Sanjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3492323/
https://www.ncbi.nlm.nih.gov/pubmed/23145098
http://dx.doi.org/10.1371/journal.pone.0049134
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author Liang, Shuo
Hu, Jingsong
Cao, Weijun
Cai, Sanjun
author_facet Liang, Shuo
Hu, Jingsong
Cao, Weijun
Cai, Sanjun
author_sort Liang, Shuo
collection PubMed
description BACKGROUND: CYP2C9 encodes a member of the cytochrome P450 superfamily of enzymes which play a central role in activating and detoxifying many carcinogens and endogenous compounds thought to be involved in the development of colorectal cancer (CRC). In the past decade, the relationship between CYP2C9 common polymorphisms (R144C and I359L) and CRC has been reported in various ethnic groups; however, these studies have yielded contradictory results. To investigate this inconsistency, we performed this meta-analysis. METHODS: Databases including Pubmed, EMBASE, Web of Science and China National Knowledge Infrastructure (CNKI) were searched to find relevant studies. Odds ratios (ORs) with 95% confidence intervals (CIs) were used to assess the strength of association. RESULTS: A total of 13 articles involving 9,463 cases and 11,416 controls were included. Overall, the summary odds ratio of CRC was 0.98 (95% CI: 0.89−1.06) and 0.99 (95% CI: 0.87−1.14) for CYP2C9 144C and 359L alleles, respectively. No significant results were observed using dominant or recessive genetic model for these polymorphisms. In the stratified analyses according to ethnicity and sex, no evidence of any gene-disease association was obtained. CONCLUSIONS: This meta-analysis suggests that the CYP2C9 may not be associated with colorectal cancer development.
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spelling pubmed-34923232012-11-09 Meta-Analysis of Cytochrome P-450 2C9 Polymorphism and Colorectal Cancer Risk Liang, Shuo Hu, Jingsong Cao, Weijun Cai, Sanjun PLoS One Research Article BACKGROUND: CYP2C9 encodes a member of the cytochrome P450 superfamily of enzymes which play a central role in activating and detoxifying many carcinogens and endogenous compounds thought to be involved in the development of colorectal cancer (CRC). In the past decade, the relationship between CYP2C9 common polymorphisms (R144C and I359L) and CRC has been reported in various ethnic groups; however, these studies have yielded contradictory results. To investigate this inconsistency, we performed this meta-analysis. METHODS: Databases including Pubmed, EMBASE, Web of Science and China National Knowledge Infrastructure (CNKI) were searched to find relevant studies. Odds ratios (ORs) with 95% confidence intervals (CIs) were used to assess the strength of association. RESULTS: A total of 13 articles involving 9,463 cases and 11,416 controls were included. Overall, the summary odds ratio of CRC was 0.98 (95% CI: 0.89−1.06) and 0.99 (95% CI: 0.87−1.14) for CYP2C9 144C and 359L alleles, respectively. No significant results were observed using dominant or recessive genetic model for these polymorphisms. In the stratified analyses according to ethnicity and sex, no evidence of any gene-disease association was obtained. CONCLUSIONS: This meta-analysis suggests that the CYP2C9 may not be associated with colorectal cancer development. Public Library of Science 2012-11-07 /pmc/articles/PMC3492323/ /pubmed/23145098 http://dx.doi.org/10.1371/journal.pone.0049134 Text en © 2012 Liang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Liang, Shuo
Hu, Jingsong
Cao, Weijun
Cai, Sanjun
Meta-Analysis of Cytochrome P-450 2C9 Polymorphism and Colorectal Cancer Risk
title Meta-Analysis of Cytochrome P-450 2C9 Polymorphism and Colorectal Cancer Risk
title_full Meta-Analysis of Cytochrome P-450 2C9 Polymorphism and Colorectal Cancer Risk
title_fullStr Meta-Analysis of Cytochrome P-450 2C9 Polymorphism and Colorectal Cancer Risk
title_full_unstemmed Meta-Analysis of Cytochrome P-450 2C9 Polymorphism and Colorectal Cancer Risk
title_short Meta-Analysis of Cytochrome P-450 2C9 Polymorphism and Colorectal Cancer Risk
title_sort meta-analysis of cytochrome p-450 2c9 polymorphism and colorectal cancer risk
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3492323/
https://www.ncbi.nlm.nih.gov/pubmed/23145098
http://dx.doi.org/10.1371/journal.pone.0049134
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