Zhang Xue-Mei, Miao Xiao-Ping, Xiong Ping, Yu Chun-Yuan, Tan Wen, Qu Shi-Ning, Sun Tong, Zhou Yi-Feng, Lin Dong-Xin
Department of Biological Sciences, North China Coal Medical College, Tangshan, Hebei 063 000, P.R. China.
Ai Zheng. 2004 Nov;23(11):1233-7.
BACKGROUND & OBJECTIVE: Matrix metalloproteinase-2 (MMP-2) and -9 (MMP-9) play important roles in the development of gastric cancer. This study was to investigate the association of functional polymorphisms in the MMP-2 and MMP-9 genes with risk of gastric cancer in a Chinese population.
MMP-2 -1306T/C,and MMP-9 -1562C/T polymorphisms in 228 patients with gastric cancer, and 774 matched healthy controls were detected by polymerase chain reaction (PCR)-based denaturing high performance liquid chromatography, and PCR-based restriction fragment length polymorphism analysis. The adjusted odds ratios (ORs) and 95% confidence intervals (CIs) were calculated using unconditional logistic regression model. The effect-modified model was used to evaluate the gene-gene interaction.
Subjects with the MMP-2 -1306CC genotype had an increased risk of developing gastric cancer compared with those with the MMP-2 -1306TT or CT genotype (adjusted OR, 1.67; 95% CI, 1.17-2.38). No significant association between MMP-9 -1562C/T polymorphism and risk of gastric cancer was observed. However, the polymorphisms in these 2 genes seem to display a gene-gene interaction, with OR of 1.72 (95% CI, 1.07-2.78) for subjects carrying both MMP-2 -1306CC and MMP-9 -1562TT or CT genotypes compared with those carrying both MMP-2 -1306TT or CT and MMP-2 -1306T/C genotypes (likelihood ratio test, P=0.02).
MMP-2 -1306T/C and MMP-9 -1562C/T polymorphisms may be associated with genetic susceptibility to gastric cancer.
基质金属蛋白酶-2(MMP-2)和-9(MMP-9)在胃癌发生发展中起重要作用。本研究旨在探讨中国人群中MMP-2和MMP-9基因功能多态性与胃癌风险的相关性。
采用基于聚合酶链反应(PCR)的变性高效液相色谱法和基于PCR的限制性片段长度多态性分析,检测228例胃癌患者及774例匹配的健康对照者的MMP-2 -1306T/C和MMP-9 -1562C/T多态性。使用非条件逻辑回归模型计算调整后的比值比(OR)和95%置信区间(CI)。采用效应修饰模型评估基因-基因相互作用。
与MMP-2 -1306TT或CT基因型者相比,MMP-2 -1306CC基因型者患胃癌的风险增加(调整后OR,1.67;95%CI,1.17-2.38)。未观察到MMP-9 -1562C/T多态性与胃癌风险之间存在显著关联。然而,这两个基因的多态性似乎存在基因-基因相互作用,携带MMP-2 -1306CC和MMP-9 -1562TT或CT基因型的受试者与携带MMP-2 -1306TT或CT和MMP-2 -1306T/C基因型的受试者相比,OR为1.72(95%CI,1.07-2.78)(似然比检验,P=0.02)。
MMP-2 -1306T/C和MMP-9 -1562C/T多态性可能与胃癌的遗传易感性相关。