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一项荟萃分析表明,MMP1 -1607(1G>2G)基因多态性与癌症风险显著增加有关。

The polymorphism MMP1 -1607 (1G>2G) is associated with a significantly increased risk of cancers from a meta-analysis.

作者信息

Lu Lili, Sun Yujiao, Li Yiqun, Wan Ping

机构信息

Department of Biology, College of Life and Environmental Sciences, Shanghai Normal University, 100 Guilin Road, 200234, Shanghai, China.

出版信息

Tumour Biol. 2015 Mar;36(3):1685-93. doi: 10.1007/s13277-014-2769-0. Epub 2014 Nov 13.

Abstract

Growing evidences show that matrix metalloproteinase 1 (MMP1) plays important roles in tumorigenesis and cancer metastasis. MMP1 -1607 1G>2G is a single nucleotide polymorphism in the promoter region of MMP1 and affects MMP1 production. Analysis of previous studies on the association of -1607 1G>2G polymorphism with different cancer types remained to be illustrated. To further assess the effect of -1607 1G>2G polymorphism on cancer risk, we performed this meta-analyses, up to September 8, 2014, of 10,640 cases and 10,915 controls from 42 published case-control designed studies. Statistical analyses were performed using STATA 11.0 software. Crude odds ratios (ORs) with 95% confidence intervals (CIs) were used to assess the strength of associations. ORs with 95% CIs for the polymorphism MMP1 -1607 1G>2G and cancer were estimated using fixed and random effects models when appropriate. Significantly increased risks were found in overall under the models of 2G vs.1G, 2G2G vs. 1G1G, 2G2G/1G2G vs. 1G1G, and 2G2G vs. 2G1G/1G1G. Significantly elevated risks were observed in colorectal adenoma under the models of 2G vs. 1G, 2G2G vs. 1G1G, 2G2G/1G2G vs. 1G1G, and 2G2G vs. 2G1G/1G1G and lung cancer and head and neck cancer under the models of 2G vs. 1G. We found that significantly elevated risks were observed in Asian population and hospital-based studies in most comparison models tested. Thus, this meta-analysis indicates that the polymorphism MMP1 -1607 1G>2G is significantly associated with a significantly increased risk of cancers and may provide evidence-based medical certificate to study the cancer susceptibility.

摘要

越来越多的证据表明,基质金属蛋白酶1(MMP1)在肿瘤发生和癌症转移中发挥着重要作用。MMP1 -1607 1G>2G是MMP1启动子区域的单核苷酸多态性,影响MMP1的产生。以往关于-1607 1G>2G多态性与不同癌症类型关联的研究分析仍有待阐明。为了进一步评估-1607 1G>2G多态性对癌症风险的影响,我们截至2014年9月8日对42项已发表的病例对照设计研究中的10640例病例和10915例对照进行了这项荟萃分析。使用STATA 11.0软件进行统计分析。采用粗比值比(OR)及95%置信区间(CI)评估关联强度。在适当情况下,使用固定效应模型和随机效应模型估计MMP1 -1607 1G>2G多态性与癌症的OR及95%CI。在2G与1G、2G2G与1G1G、2G2G/1G2G与1G1G以及2G2G与2G1G/1G1G模型下,总体风险显著增加。在2G与1G、2G2G与1G1G、2G2G/1G2G与1G1G以及2G2G与2G1G/1G1G模型下,结直肠腺瘤风险显著升高;在2G与1G模型下,肺癌和头颈癌风险显著升高。我们发现,在大多数测试的比较模型中,亚洲人群和基于医院的研究中风险显著升高。因此,这项荟萃分析表明,MMP1 -1607 1G>2G多态性与癌症风险显著增加显著相关,可能为研究癌症易感性提供循证医学依据。

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