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Association of CTLA-4 gene polymorphisms with sporadic breast cancer in Chinese Han population

BACKGROUND: The host immunogenetic background plays an important role in the development of breast cancer. Cytotoxic T-lymphocyte antigen-4 (CTLA-4) is a molecule expressed predominantly on activated T cells and is important during the down-regulation of T-cell activation. To evaluate the potential...

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Autores principales: Wang, Lihong, Li, Dalin, Fu, Zhenkun, Li, Heng, Jiang, Wei, Li, Dianjun
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2001196/
https://www.ncbi.nlm.nih.gov/pubmed/17825114
http://dx.doi.org/10.1186/1471-2407-7-173
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author Wang, Lihong
Li, Dalin
Fu, Zhenkun
Li, Heng
Jiang, Wei
Li, Dianjun
author_facet Wang, Lihong
Li, Dalin
Fu, Zhenkun
Li, Heng
Jiang, Wei
Li, Dianjun
author_sort Wang, Lihong
collection PubMed
description BACKGROUND: The host immunogenetic background plays an important role in the development of breast cancer. Cytotoxic T-lymphocyte antigen-4 (CTLA-4) is a molecule expressed predominantly on activated T cells and is important during the down-regulation of T-cell activation. To evaluate the potential influences of CTLA-4 gene polymorphisms on breast cancer risk, a case-control study was conducted in Han women of Northeast China. METHODS: We genotyped CTLA-4 variants (-1661 G/A, -658 T/C, -318 T/C, +49 G/A and CT60 G/A) to tag all common haplotypes (≥ 1% frequency) in 117 Chinese breast cancer cases and 148 age/sex matched healthy individuals. Genotypes were determined by the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. Data was analyzed using the Chi-square test and Haploview software. RESULTS: The frequency of CTLA-4 -1661G allele, -318T allele and CT60G allele carriers was significantly higher in patients than in controls (P = 0.0057, OR 1.91, 95% CI 1.21–3.02; P = 0.0031, OR 2.39, 95% CI 1.34–4.27; P = 0.023, OR 1.52, 95% CI 1.06–2.17, respectively). The -658T allele carrier frequency was significantly lower than in controls (P = 0.0000082, OR 0.17, 95% CI 0.08–0.37), whereas the +49A allele was significantly associated with tumor size in patients (P = 0.0033). Two common CTLA-4 haplotypes, ATCGA and ATCAG, were higher in healthy controls than patients (P = 0.0026, OR 0.17, 95% CI 0.05–0.54; P = 0.034, OR 0.12, 95% CI 0.02–0.92, respectively). A strong association was observed between tumor size and the ACCAA, ACCAG and ACCGA haplotypes (P = 0.0032, P = 0.0000031 and P = 0.017). CONCLUSION: These results suggest that polymorphisms of the CTLA-4 gene may modify individual susceptibility to and progression of breast cancer in Chinese Han women.
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spelling pubmed-20011962007-10-06 Association of CTLA-4 gene polymorphisms with sporadic breast cancer in Chinese Han population Wang, Lihong Li, Dalin Fu, Zhenkun Li, Heng Jiang, Wei Li, Dianjun BMC Cancer Research Article BACKGROUND: The host immunogenetic background plays an important role in the development of breast cancer. Cytotoxic T-lymphocyte antigen-4 (CTLA-4) is a molecule expressed predominantly on activated T cells and is important during the down-regulation of T-cell activation. To evaluate the potential influences of CTLA-4 gene polymorphisms on breast cancer risk, a case-control study was conducted in Han women of Northeast China. METHODS: We genotyped CTLA-4 variants (-1661 G/A, -658 T/C, -318 T/C, +49 G/A and CT60 G/A) to tag all common haplotypes (≥ 1% frequency) in 117 Chinese breast cancer cases and 148 age/sex matched healthy individuals. Genotypes were determined by the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. Data was analyzed using the Chi-square test and Haploview software. RESULTS: The frequency of CTLA-4 -1661G allele, -318T allele and CT60G allele carriers was significantly higher in patients than in controls (P = 0.0057, OR 1.91, 95% CI 1.21–3.02; P = 0.0031, OR 2.39, 95% CI 1.34–4.27; P = 0.023, OR 1.52, 95% CI 1.06–2.17, respectively). The -658T allele carrier frequency was significantly lower than in controls (P = 0.0000082, OR 0.17, 95% CI 0.08–0.37), whereas the +49A allele was significantly associated with tumor size in patients (P = 0.0033). Two common CTLA-4 haplotypes, ATCGA and ATCAG, were higher in healthy controls than patients (P = 0.0026, OR 0.17, 95% CI 0.05–0.54; P = 0.034, OR 0.12, 95% CI 0.02–0.92, respectively). A strong association was observed between tumor size and the ACCAA, ACCAG and ACCGA haplotypes (P = 0.0032, P = 0.0000031 and P = 0.017). CONCLUSION: These results suggest that polymorphisms of the CTLA-4 gene may modify individual susceptibility to and progression of breast cancer in Chinese Han women. BioMed Central 2007-09-10 /pmc/articles/PMC2001196/ /pubmed/17825114 http://dx.doi.org/10.1186/1471-2407-7-173 Text en Copyright © 2007 Wang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wang, Lihong
Li, Dalin
Fu, Zhenkun
Li, Heng
Jiang, Wei
Li, Dianjun
Association of CTLA-4 gene polymorphisms with sporadic breast cancer in Chinese Han population
title Association of CTLA-4 gene polymorphisms with sporadic breast cancer in Chinese Han population
title_full Association of CTLA-4 gene polymorphisms with sporadic breast cancer in Chinese Han population
title_fullStr Association of CTLA-4 gene polymorphisms with sporadic breast cancer in Chinese Han population
title_full_unstemmed Association of CTLA-4 gene polymorphisms with sporadic breast cancer in Chinese Han population
title_short Association of CTLA-4 gene polymorphisms with sporadic breast cancer in Chinese Han population
title_sort association of ctla-4 gene polymorphisms with sporadic breast cancer in chinese han population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2001196/
https://www.ncbi.nlm.nih.gov/pubmed/17825114
http://dx.doi.org/10.1186/1471-2407-7-173
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