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基质金属蛋白酶2启动子区的单核苷酸多态性与中国南方广东地区鼻咽癌的高风险密切相关。

A single nucleotide polymorphism in the matrix metalloproteinase 2 promoter is closely associated with high risk of nasopharyngeal carcinoma in Cantonese from southern China.

作者信息

Shao Jian-Yong, Cao Yun, Miao Xiao-Ping, Huang Ma-Yan, Deng Ling, Hao Jian-Jun, Liang Xiao-Man, Hu Li-Fu, Ernberg Ingemar, Lin Dong-Xin, Zeng Yi-Xin

机构信息

State Key Laboratory of Oncology in South China, Guangzhou, Guangdong 510060, P. R. China.

出版信息

Chin J Cancer. 2011 Sep;30(9):620-6. doi: 10.5732/cjc.010.10592.

Abstract

Matrix metalloproteinase 2 (MMP2) has been shown to play an important role in several steps of cancer development. The -1306C/T polymorphism of the MMP2 gene displays a strikingly lower promoter activity than the T allele, and the CC genotype in the MMP2 promoter has been reported to associate with the development of several cancers. To assess the contribution of the MMP2 -1306C/T polymorphism to the risk of nasopharyngeal carcinoma (NPC), we conducted a case-control study and analyzed MMP2 genotypes in 370 patients with NPC and 390 frequency-matched controls using real-time PCR-based TaqMan allele analysis. We found that subjects with the CC genotype had an increased risk (OR = 1.55, 95% CI = 1.05-2.27) of developing NPC compared to those with the CT or TT genotypes. Furthermore, we found that the risk of NPC was markedly increased in subjects who were smokers (OR = 15.04, 95% CI = 6.65-33.99), heavy smokers who smoked ≥ 20 pack-years (OR = 18.66, 95% CI = 7.67-45.38), or young (<60 years) at diagnosis (OR = 1.52, 95% CI = 1.01-2.29). Our results provide molecular epidemiological evidence that the MMP2 -1306C/T promoter polymorphism is associated with NPC risk, and this association is especially noteworthy in heavy smokers.

摘要

基质金属蛋白酶2(MMP2)已被证明在癌症发展的多个步骤中起重要作用。MMP2基因的-1306C/T多态性显示出比T等位基因显著更低的启动子活性,并且MMP2启动子中的CC基因型已被报道与多种癌症的发生有关。为了评估MMP2 -1306C/T多态性对鼻咽癌(NPC)风险的影响,我们进行了一项病例对照研究,并使用基于实时PCR的TaqMan等位基因分析方法,对370例NPC患者和390例频率匹配的对照者的MMP2基因型进行了分析。我们发现,与CT或TT基因型的受试者相比,CC基因型的受试者患NPC的风险增加(OR = 1.55,95% CI = 1.05 - 2.27)。此外,我们发现吸烟者(OR = 15.04,95% CI = 6.65 - 33.99)、吸烟量≥20包年的重度吸烟者(OR = 18.66,95% CI = 7.67 - 45.38)或诊断时年龄较轻(<60岁)的受试者患NPC的风险显著增加(OR = 1.52,95% CI = 1.01 - 2.29)。我们的结果提供了分子流行病学证据,表明MMP2 -1306C/T启动子多态性与NPC风险相关,并且这种关联在重度吸烟者中尤为值得注意。

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本文引用的文献

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