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基质金属蛋白酶-2基因启动子(-1306C/T)中的功能性多态性与贲门腺癌的发生风险相关,但与转移风险无关。

A functional polymorphism in the matrix metalloproteinase-2 gene promoter (-1306C/T) is associated with risk of development but not metastasis of gastric cardia adenocarcinoma.

作者信息

Miao Xiaoping, Yu Chunyuan, Tan Wen, Xiong Ping, Liang Gang, Lu Wenfu, Lin Dongxin

机构信息

Department of Etiology and Carcinogenesis, Cancer Institute, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.

出版信息

Cancer Res. 2003 Jul 15;63(14):3987-90.

Abstract

Matrix metalloproteinase-2 (MMP-2) has been shown to play an importantrole in multiple ways to all stages of cancer initiation and development.We have reported previously a strong association between a functional single nucleotide polymorphism (-1306C/T) in the MMP2 promoter and risk of lung cancer (C. Yu et al., Cancer Res., 62: 6430-6433, 2002). This case control study was to assess the contribution of this MMP2 polymorphism to risk of development and metastasis of gastric cardia adenocarcinoma (GCA). MMP2 genotypes were determined by PCR-based denaturing high-performance liquid chromatography analysis and direct DNA sequencing in 356 patients with GCA and 789 frequency-matched controls in an ethnic Chinese population. We found that subjects with the CC genotype had >3-fold increased risk [adjusted odds ratio 3.36, 95% confidence interval 2.34-4.97] for developing GCA compared with those with the variant CT or TT genotype. Furthermore, the increased risk was found to be more pronounced in smokers and younger subjects. However, no significant association was demonstrated between the MMP2 polymorphism and risk of metastasis of the cancer at the time of diagnosis, with the odds ratio being 0.90 (95% confidence interval 0.36-2.20) for the CC genotype. These findings are consistent with our initial observation for lung cancer and further support the hypothesis that MMP2 genotype may influence individual susceptibility to the development of certain cancer.

摘要

基质金属蛋白酶-2(MMP-2)已被证明在癌症发生和发展的各个阶段都以多种方式发挥重要作用。我们之前报道过,MMP2启动子中的一个功能性单核苷酸多态性(-1306C/T)与肺癌风险之间存在密切关联(C. Yu等人,《癌症研究》,62: 6430 - 6433,2002年)。本病例对照研究旨在评估这种MMP2多态性对贲门腺癌(GCA)发生和转移风险的影响。通过基于聚合酶链反应的变性高效液相色谱分析和直接DNA测序,在一个中国汉族人群的356例GCA患者和789例频率匹配的对照中确定了MMP2基因型。我们发现,与携带变异型CT或TT基因型的受试者相比,携带CC基因型的受试者发生GCA的风险增加了3倍以上[调整后的优势比为3.36,95%置信区间为2.34 - 4.97]。此外,在吸烟者和年轻受试者中,这种增加的风险更为明显。然而,在诊断时,未发现MMP2多态性与癌症转移风险之间存在显著关联,CC基因型的优势比为0.90(95%置信区间为0.36 - 2.20)。这些发现与我们最初对肺癌的观察结果一致,并进一步支持了MMP2基因型可能影响个体对某些癌症发生易感性的假说。

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