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Cytochrome P450 1A1 gene polymorphisms and cervical cancer risk: A systematic review and meta-analysis

OBJECTIVE: This meta-analysis aims to examine whether the MspI and Ile462Val polymorphisms of cytochrome P450 1A1 (CYP1A1) are associated with cervical cancer risk. METHODS: Eligible case–control studies were identified dated until July 2017. Pooled odds ratios (ORs) were used to assess the strength...

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Autores principales: Ding, Bo, Sun, Wei, Han, Suping, Cai, Yunlang, Ren, Mulan, Shen, Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5895380/
https://www.ncbi.nlm.nih.gov/pubmed/29595663
http://dx.doi.org/10.1097/MD.0000000000010210
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author Ding, Bo
Sun, Wei
Han, Suping
Cai, Yunlang
Ren, Mulan
Shen, Yang
author_facet Ding, Bo
Sun, Wei
Han, Suping
Cai, Yunlang
Ren, Mulan
Shen, Yang
author_sort Ding, Bo
collection PubMed
description OBJECTIVE: This meta-analysis aims to examine whether the MspI and Ile462Val polymorphisms of cytochrome P450 1A1 (CYP1A1) are associated with cervical cancer risk. METHODS: Eligible case–control studies were identified dated until July 2017. Pooled odds ratios (ORs) were used to assess the strength of the association between the two variants and cervical cancer risk. RESULTS: Thirteen studies were eligible (2148 cases and 2252 controls) concerning MspI polymorphism and 8 studies were eligible (1466 cases and 1690 controls) for Ile462Val polymorphism. MspI polymorphism seemed to result in cervical cancer risk in any genetic model (C allele vs T allele: OR = 1.44, 95% confidence interval [CI] = 1.16–1.79; heterozygous model: OR = 1.40, 95% CI = 1.08–1.82; homozygous model: OR = 2.22, 95% CI = 1.48–3.33, dominant model: OR = 1.50, 95% CI = 1.14–1.98 and recessive model: OR = 1.80, 95% CI = 1.35–2.41); similar significantly increased risk was found among Caucasians and Asians. Ile462Val polymorphism was associated with elevated cervical cancer risk (Val allele vs Ile allele: OR = 1.85, 95% CI = 1.27–2.67; heterozygous model: OR = 1.42, 95% CI = 1.28–1.61; homozygous model: OR = 2.94, 95% CI = 1.15–7.54; dominant model: OR = 2.00, 95% CI = 1.33–3.00); this finding was replicated upon Caucasian population. CONCLUSION: This meta-analysis demonstrated that polymorphisms in MspI and Ile462Val of CYP1A1 were risk factors for developing cervical cancer.
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spelling pubmed-58953802018-04-18 Cytochrome P450 1A1 gene polymorphisms and cervical cancer risk: A systematic review and meta-analysis Ding, Bo Sun, Wei Han, Suping Cai, Yunlang Ren, Mulan Shen, Yang Medicine (Baltimore) 5700 OBJECTIVE: This meta-analysis aims to examine whether the MspI and Ile462Val polymorphisms of cytochrome P450 1A1 (CYP1A1) are associated with cervical cancer risk. METHODS: Eligible case–control studies were identified dated until July 2017. Pooled odds ratios (ORs) were used to assess the strength of the association between the two variants and cervical cancer risk. RESULTS: Thirteen studies were eligible (2148 cases and 2252 controls) concerning MspI polymorphism and 8 studies were eligible (1466 cases and 1690 controls) for Ile462Val polymorphism. MspI polymorphism seemed to result in cervical cancer risk in any genetic model (C allele vs T allele: OR = 1.44, 95% confidence interval [CI] = 1.16–1.79; heterozygous model: OR = 1.40, 95% CI = 1.08–1.82; homozygous model: OR = 2.22, 95% CI = 1.48–3.33, dominant model: OR = 1.50, 95% CI = 1.14–1.98 and recessive model: OR = 1.80, 95% CI = 1.35–2.41); similar significantly increased risk was found among Caucasians and Asians. Ile462Val polymorphism was associated with elevated cervical cancer risk (Val allele vs Ile allele: OR = 1.85, 95% CI = 1.27–2.67; heterozygous model: OR = 1.42, 95% CI = 1.28–1.61; homozygous model: OR = 2.94, 95% CI = 1.15–7.54; dominant model: OR = 2.00, 95% CI = 1.33–3.00); this finding was replicated upon Caucasian population. CONCLUSION: This meta-analysis demonstrated that polymorphisms in MspI and Ile462Val of CYP1A1 were risk factors for developing cervical cancer. Wolters Kluwer Health 2018-03-30 /pmc/articles/PMC5895380/ /pubmed/29595663 http://dx.doi.org/10.1097/MD.0000000000010210 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NoDerivatives License 4.0, which allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to the author. http://creativecommons.org/licenses/by-nd/4.0
spellingShingle 5700
Ding, Bo
Sun, Wei
Han, Suping
Cai, Yunlang
Ren, Mulan
Shen, Yang
Cytochrome P450 1A1 gene polymorphisms and cervical cancer risk: A systematic review and meta-analysis
title Cytochrome P450 1A1 gene polymorphisms and cervical cancer risk: A systematic review and meta-analysis
title_full Cytochrome P450 1A1 gene polymorphisms and cervical cancer risk: A systematic review and meta-analysis
title_fullStr Cytochrome P450 1A1 gene polymorphisms and cervical cancer risk: A systematic review and meta-analysis
title_full_unstemmed Cytochrome P450 1A1 gene polymorphisms and cervical cancer risk: A systematic review and meta-analysis
title_short Cytochrome P450 1A1 gene polymorphisms and cervical cancer risk: A systematic review and meta-analysis
title_sort cytochrome p450 1a1 gene polymorphisms and cervical cancer risk: a systematic review and meta-analysis
topic 5700
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5895380/
https://www.ncbi.nlm.nih.gov/pubmed/29595663
http://dx.doi.org/10.1097/MD.0000000000010210
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