Fang Wen-Liang, Liang Wei-Bo, Gao Lin-Bo, Zhou Bin, Xiao Feng-Li, Zhang Lin
Central Laboratory of Clinical College, Anhui Medical University, Hefei 230601, P. R. China.
Iran J Allergy Asthma Immunol. 2013 Jul 9;12(3):203-10.
Matrix Metalloproteinases (MMPs) play an important role in gastric cancer (GC). Accumulated evidence suggests that functional MMP-1 and MMP-7 gene polymorphisms are associated with several tumors. The aim of this study was to investigate two single nucleotide polymorphisms, MMP-1 -1607 1G/2G and MMP-7 -181 A/G, and their potential relationship with GC. We examined 246 GC patients and 252 age-and sex-matched controls from Sichuan province in China. Genotypes were determined using a polymerase chain reaction-restriction fragment length polymorphism strategy and DNA sequencing. We also performed a meta-analysis of relevant studies, involving 1084 cases and 1721 controls, to place our findings in a broader context. No significant relationship was observed between the MMP-1 -1607 1G/2G alleles and genotypes and the risk of GC. There were significant differences in the genotypes and allele distributions of the -181 A/G polymorphism of the MMP-7 gene between cases and controls. The -181 A allele carriers had a significantly increased risk of GC compared with -181 G allele carriers (OR=3.051, 95% CI, 1.475-6.310, P=0.002), and the AA genotype of -181 A/G was associated with an increased risk of GC compared with the AG genotype (OR=3.189, 95% CI, 1.523-6.676, P=0.001). A meta-analysis of six studies also showed a significant risk of GC associated with MMP-7 polymorphism.
基质金属蛋白酶(MMPs)在胃癌(GC)中起重要作用。越来越多的证据表明,功能性MMP-1和MMP-7基因多态性与多种肿瘤相关。本研究的目的是调查两个单核苷酸多态性,即MMP-1 -1607 1G/2G和MMP-7 -181 A/G,以及它们与GC的潜在关系。我们检测了来自中国四川省的246例GC患者和252例年龄及性别匹配的对照。使用聚合酶链反应-限制性片段长度多态性策略和DNA测序确定基因型。我们还对相关研究进行了荟萃分析,涉及1084例病例和1721例对照,以便将我们的研究结果置于更广泛的背景中。未观察到MMP-1 -1607 1G/2G等位基因和基因型与GC风险之间存在显著关系。MMP-7基因-181 A/G多态性的基因型和等位基因分布在病例组和对照组之间存在显著差异。与-181 G等位基因携带者相比,-181 A等位基因携带者患GC的风险显著增加(OR=3.051,95%CI,1.475-6.310,P=0.002),并且-181 A/G的AA基因型与AG基因型相比,患GC的风险增加(OR=3.189,95%CI,1.523-6.676,P=0.001)。六项研究的荟萃分析也显示MMP-7多态性与GC风险显著相关。