Lu Lili, Sun Yujiao, Li Yiqun, Wan Ping
Department of Biology, College of Life and Environmental Sciences, Shanghai Normal University, 100 Guilin Road, 200234, Shanghai, China.
Tumour Biol. 2015 Mar;36(3):1685-93. doi: 10.1007/s13277-014-2769-0. Epub 2014 Nov 13.
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.
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。