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CXCL12基因G801A多态性与癌症易感性相关:一项荟萃分析

CXCL12 G801A polymorphism contributes to cancer susceptibility: a meta-analysis.

作者信息

Ma X Y, Jin Y, Sun H M, Yu L, Bai J, Chen F, Fu S B

机构信息

Laboratory of Medical Genetics, Harbin Medical University, Harbin, China.

出版信息

Cell Mol Biol (Noisy-le-grand). 2012 Jun 30;58 Suppl:OL1702-8.

Abstract

CXCL12 is an important alpha-chemokine that regulates many essential biological processes including tumor development and metastasis. The CXCL12 G801A polymorphism is associated with multiple kinds of malignant cancer, but the associations are inconsistent. To derive a more precise estimation of the relationship, we conducted a meta-analysis of 16 publications with 2,888 cases and 3,611 controls. We used the odds ratio (OR) corresponding to 95% confidence interval (CI) to estimate the strength of association. The increased risk of overall cancer was found in the homozygote comparison (AA vs. GG, OR=1.43, 95℅CI=1.07-1.91), the recessive model (AA vs. GG+GA, OR=1.26, 95℅CI=1.03-1.54), and the dominant model (GA+AA vs. GG, OR=1.35, 95℅CI=1.15-1.58). In the stratified analyses, the associations were significant in breast cancer, Asians and hospital-based controls. In conclusion, this meta-analysis suggests that the CXCL12 G801A polymorphism may be a risk factor of cancer, especially in the subgroups of breast cancer, Asians and hospital-based controls.

摘要

CXCL12是一种重要的α趋化因子,可调节包括肿瘤发生和转移在内的许多重要生物学过程。CXCL12 G801A基因多态性与多种恶性肿瘤相关,但这些关联并不一致。为了更精确地估计这种关系,我们对16篇文献进行了荟萃分析,共纳入2888例病例和3611例对照。我们使用对应95%置信区间(CI)的优势比(OR)来估计关联强度。在纯合子比较(AA与GG,OR = 1.43,95%CI = 1.07 - 1.91)、隐性模型(AA与GG + GA,OR = 1.26,95%CI = 1.03 - 1.54)和显性模型(GA + AA与GG,OR = 1.35,95%CI = 1.15 - 1.58)中发现总体癌症风险增加。在分层分析中,乳腺癌、亚洲人群和基于医院的对照中关联显著。总之,这项荟萃分析表明CXCL12 G801A基因多态性可能是癌症的一个危险因素,尤其是在乳腺癌、亚洲人群和基于医院的对照亚组中。

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