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CXCL12 G801A polymorphism and cancer risk: An updated meta-analysis / 华中科技大学学报(医学)(英德文版)
Journal of Huazhong University of Science and Technology (Medical Sciences) ; (6): 319-326, 2015.
Artigo em Inglês | WPRIM | ID: wpr-331066
ABSTRACT
Many studies have reported the relationship between CXCL12 G801A polymorphism and cancer risk, with conflicting results. In this study, we tried to clarify the possibility that this polymorphism may increase cancer risk by conducting an updated meta-analysis. PubMed and EMbase were searched for case-control studies regarding the association of the gene polymorphism and cancer risk. Data were extracted and odds ratios (ORs) with 95% confidence intervals (95% CIs) were used to assess the strength of the association. Heterogeneity among articles and publication bias was also assessed. Significantly increased risk for cancer was found (A vs. G OR=1.26, 95% CI=1.13-1.40, P<0.01; AA+AG vs. GG OR=1.33, 95% CI=1.16-1.52, P<0.01). In subgroup analysis, statistically elevated cancer risk was found in both Asian and Caucasian populations (for Asian, AA+AG vs. GG OR=1.74, 95% CI=1.22-2.47, P<0.01; for Caucasian, AA+AG vs. GG OR=1.24, 95% CI=1.09-1.42, P<0.01). Our result indicated that CXCL12 G801A polymorphism is a risk factor for cancer. To validate the finding, further large-size case-control studies are warranted.
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Patologia / Razão de Chances / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Povo Asiático / População Branca / Etnologia / Quimiocina CXCL12 / Genética / Neoplasias Tipo de estudo: Estudo de etiologia / Estudo observacional / Fatores de risco / Revisões Sistemáticas Avaliadas Limite: Humanos Idioma: Inglês Revista: Journal of Huazhong University of Science and Technology (Medical Sciences) Ano de publicação: 2015 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Patologia / Razão de Chances / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Povo Asiático / População Branca / Etnologia / Quimiocina CXCL12 / Genética / Neoplasias Tipo de estudo: Estudo de etiologia / Estudo observacional / Fatores de risco / Revisões Sistemáticas Avaliadas Limite: Humanos Idioma: Inglês Revista: Journal of Huazhong University of Science and Technology (Medical Sciences) Ano de publicação: 2015 Tipo de documento: Artigo