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Association between CYP2E1 genetic polymorphisms and urinary cancer risk: a meta-analysis
OBJECTIVE: Studies investigating the contribution of Cytochrome P4502E1 (CYP2E1) polymorphisms to the etiology of urinary cancer draw inconsistent conclusions. Thus, we performed a meta-analysis to evaluate the association between CYP2E1 Rsa I/Pst I and Dra I polymorphisms and urinary cancer suscept...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5689730/ https://www.ncbi.nlm.nih.gov/pubmed/29156840 http://dx.doi.org/10.18632/oncotarget.20993 |
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author | Fang, Zhiqing Wu, Yun Zhang, Ning |
author_facet | Fang, Zhiqing Wu, Yun Zhang, Ning |
author_sort | Fang, Zhiqing |
collection | PubMed |
description | OBJECTIVE: Studies investigating the contribution of Cytochrome P4502E1 (CYP2E1) polymorphisms to the etiology of urinary cancer draw inconsistent conclusions. Thus, we performed a meta-analysis to evaluate the association between CYP2E1 Rsa I/Pst I and Dra I polymorphisms and urinary cancer susceptibility. MATERIALS AND METHODS: Meta-analysis based on the eligible case-control studies that assess the association of CYP2E1 Rsa I/Pst I and Dra I polymorphisms with urinary cancer was conducted. Subgroup analyses based on ethnicity and cancer type were also carried out. Odds ratios (OR) and 95% confidence intervals (95% CI) were calculated to evaluate the strength of the associations between the two polymorphisms. Funnel plot and Begg’s test were used for publication bias diagnosis. RESULTS: We found decreased urinary cancer risk among subjects carrying CYP2E1 RsaI/PstI c1c2 + c2c2 genotype and c2 allele (OR = 0.73, 95% CI = 0.68–0.79 and OR = 0.79, 95% CI = 0.74–0.85, respectively), with 3,301 cases and 3,786 controls from 14 studies. We also observed a significant difference in c1c2 + c2c2 vs. c1c1 and c2 vs. c1 among Asians (OR = 0.68, 95% CI = 0.60–0.78 and OR = 0.75, 95% CI = 0.66–0.85, respectively). However, the meta-analysis based on 5 eligible studies showed no significant association between CYP2E1 Dra I polymorphism and urinary cancer susceptibility in either dominant model or the allele model. CONCLUSIONS: Our meta-analysis concluded that CYP2E1 Rsa I/Pst I polymorphism correlates with urinary cancers risk in Asian population; while CYP2E1 Dra I polymorphism might be not significantly associated with the urinary cancer risks. Large and well-designed studies are needed to confirm these results. |
format | Online Article Text |
id | pubmed-5689730 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56897302017-11-17 Association between CYP2E1 genetic polymorphisms and urinary cancer risk: a meta-analysis Fang, Zhiqing Wu, Yun Zhang, Ning Oncotarget Meta-Analysis OBJECTIVE: Studies investigating the contribution of Cytochrome P4502E1 (CYP2E1) polymorphisms to the etiology of urinary cancer draw inconsistent conclusions. Thus, we performed a meta-analysis to evaluate the association between CYP2E1 Rsa I/Pst I and Dra I polymorphisms and urinary cancer susceptibility. MATERIALS AND METHODS: Meta-analysis based on the eligible case-control studies that assess the association of CYP2E1 Rsa I/Pst I and Dra I polymorphisms with urinary cancer was conducted. Subgroup analyses based on ethnicity and cancer type were also carried out. Odds ratios (OR) and 95% confidence intervals (95% CI) were calculated to evaluate the strength of the associations between the two polymorphisms. Funnel plot and Begg’s test were used for publication bias diagnosis. RESULTS: We found decreased urinary cancer risk among subjects carrying CYP2E1 RsaI/PstI c1c2 + c2c2 genotype and c2 allele (OR = 0.73, 95% CI = 0.68–0.79 and OR = 0.79, 95% CI = 0.74–0.85, respectively), with 3,301 cases and 3,786 controls from 14 studies. We also observed a significant difference in c1c2 + c2c2 vs. c1c1 and c2 vs. c1 among Asians (OR = 0.68, 95% CI = 0.60–0.78 and OR = 0.75, 95% CI = 0.66–0.85, respectively). However, the meta-analysis based on 5 eligible studies showed no significant association between CYP2E1 Dra I polymorphism and urinary cancer susceptibility in either dominant model or the allele model. CONCLUSIONS: Our meta-analysis concluded that CYP2E1 Rsa I/Pst I polymorphism correlates with urinary cancers risk in Asian population; while CYP2E1 Dra I polymorphism might be not significantly associated with the urinary cancer risks. Large and well-designed studies are needed to confirm these results. Impact Journals LLC 2017-09-18 /pmc/articles/PMC5689730/ /pubmed/29156840 http://dx.doi.org/10.18632/oncotarget.20993 Text en Copyright: © 2017 Fang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Meta-Analysis Fang, Zhiqing Wu, Yun Zhang, Ning Association between CYP2E1 genetic polymorphisms and urinary cancer risk: a meta-analysis |
title | Association between CYP2E1 genetic polymorphisms and urinary cancer risk: a meta-analysis |
title_full | Association between CYP2E1 genetic polymorphisms and urinary cancer risk: a meta-analysis |
title_fullStr | Association between CYP2E1 genetic polymorphisms and urinary cancer risk: a meta-analysis |
title_full_unstemmed | Association between CYP2E1 genetic polymorphisms and urinary cancer risk: a meta-analysis |
title_short | Association between CYP2E1 genetic polymorphisms and urinary cancer risk: a meta-analysis |
title_sort | association between cyp2e1 genetic polymorphisms and urinary cancer risk: a meta-analysis |
topic | Meta-Analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5689730/ https://www.ncbi.nlm.nih.gov/pubmed/29156840 http://dx.doi.org/10.18632/oncotarget.20993 |
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