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Lack of Association between Cytotoxic T-lymphocyte Antigen 4 (CTLA-4) -1722T/C (rs733618) Polymorphism and Cancer Risk: From a Case-Control Study to a Meta-Analysis

BACKGROUND: The association between cytotoxic T-lymphocyte antigen 4 (CTLA-4) gene -1722T/C polymorphism (rs733618) and cancer has been widely assessed, and a definitive conclusion remains elusive. We first performed a hospital based case-control study to measure this association of esophageal cance...

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Autores principales: Tang, Weifeng, Qiu, Hao, Jiang, Heping, Sun, Bin, Wang, Lixin, Yin, Jun, Gu, Haiyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3978075/
https://www.ncbi.nlm.nih.gov/pubmed/24710335
http://dx.doi.org/10.1371/journal.pone.0094039
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author Tang, Weifeng
Qiu, Hao
Jiang, Heping
Sun, Bin
Wang, Lixin
Yin, Jun
Gu, Haiyong
author_facet Tang, Weifeng
Qiu, Hao
Jiang, Heping
Sun, Bin
Wang, Lixin
Yin, Jun
Gu, Haiyong
author_sort Tang, Weifeng
collection PubMed
description BACKGROUND: The association between cytotoxic T-lymphocyte antigen 4 (CTLA-4) gene -1722T/C polymorphism (rs733618) and cancer has been widely assessed, and a definitive conclusion remains elusive. We first performed a hospital based case-control study to measure this association of esophageal cancer with CTLA-4 -1722T/C polymorphism in Han Chinese population, and then carried out a meta-analysis to obtain a comprehensive evaluation for this issue. METHODOLOGY/PRINCIPAL FINDINGS: This case-control study involved 629 esophageal squamous cell carcinoma (ESCC) cases and 686 age and gender well matched cancer-free controls. PCR-LDR (polymerase chain reaction-ligase detection reactions) method was used to identify genotypes. Meta-analysis was conducted by STATA (v12.0) software. This case-control study showed no significant difference in the genotype and allele distributions of CTLA-4 -1722T/C polymorphism between esophageal cancer cases and control subjects, in accord with the findings of the further meta-analysis in all genetic models. Evidence of large heterogeneity was observed among all eligible studies in the recessive model. Further subgroup analyses by ethnicity, cancer type and system, detected null associations in this meta-analysis. CONCLUSION: This case-control study and the further meta-analysis, failed to identify the association between CTLA-4 -1722T/C polymorphism and cancer risk.
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spelling pubmed-39780752014-04-11 Lack of Association between Cytotoxic T-lymphocyte Antigen 4 (CTLA-4) -1722T/C (rs733618) Polymorphism and Cancer Risk: From a Case-Control Study to a Meta-Analysis Tang, Weifeng Qiu, Hao Jiang, Heping Sun, Bin Wang, Lixin Yin, Jun Gu, Haiyong PLoS One Research Article BACKGROUND: The association between cytotoxic T-lymphocyte antigen 4 (CTLA-4) gene -1722T/C polymorphism (rs733618) and cancer has been widely assessed, and a definitive conclusion remains elusive. We first performed a hospital based case-control study to measure this association of esophageal cancer with CTLA-4 -1722T/C polymorphism in Han Chinese population, and then carried out a meta-analysis to obtain a comprehensive evaluation for this issue. METHODOLOGY/PRINCIPAL FINDINGS: This case-control study involved 629 esophageal squamous cell carcinoma (ESCC) cases and 686 age and gender well matched cancer-free controls. PCR-LDR (polymerase chain reaction-ligase detection reactions) method was used to identify genotypes. Meta-analysis was conducted by STATA (v12.0) software. This case-control study showed no significant difference in the genotype and allele distributions of CTLA-4 -1722T/C polymorphism between esophageal cancer cases and control subjects, in accord with the findings of the further meta-analysis in all genetic models. Evidence of large heterogeneity was observed among all eligible studies in the recessive model. Further subgroup analyses by ethnicity, cancer type and system, detected null associations in this meta-analysis. CONCLUSION: This case-control study and the further meta-analysis, failed to identify the association between CTLA-4 -1722T/C polymorphism and cancer risk. Public Library of Science 2014-04-07 /pmc/articles/PMC3978075/ /pubmed/24710335 http://dx.doi.org/10.1371/journal.pone.0094039 Text en © 2014 Tang 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
Tang, Weifeng
Qiu, Hao
Jiang, Heping
Sun, Bin
Wang, Lixin
Yin, Jun
Gu, Haiyong
Lack of Association between Cytotoxic T-lymphocyte Antigen 4 (CTLA-4) -1722T/C (rs733618) Polymorphism and Cancer Risk: From a Case-Control Study to a Meta-Analysis
title Lack of Association between Cytotoxic T-lymphocyte Antigen 4 (CTLA-4) -1722T/C (rs733618) Polymorphism and Cancer Risk: From a Case-Control Study to a Meta-Analysis
title_full Lack of Association between Cytotoxic T-lymphocyte Antigen 4 (CTLA-4) -1722T/C (rs733618) Polymorphism and Cancer Risk: From a Case-Control Study to a Meta-Analysis
title_fullStr Lack of Association between Cytotoxic T-lymphocyte Antigen 4 (CTLA-4) -1722T/C (rs733618) Polymorphism and Cancer Risk: From a Case-Control Study to a Meta-Analysis
title_full_unstemmed Lack of Association between Cytotoxic T-lymphocyte Antigen 4 (CTLA-4) -1722T/C (rs733618) Polymorphism and Cancer Risk: From a Case-Control Study to a Meta-Analysis
title_short Lack of Association between Cytotoxic T-lymphocyte Antigen 4 (CTLA-4) -1722T/C (rs733618) Polymorphism and Cancer Risk: From a Case-Control Study to a Meta-Analysis
title_sort lack of association between cytotoxic t-lymphocyte antigen 4 (ctla-4) -1722t/c (rs733618) polymorphism and cancer risk: from a case-control study to a meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3978075/
https://www.ncbi.nlm.nih.gov/pubmed/24710335
http://dx.doi.org/10.1371/journal.pone.0094039
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