Li Guojun, Zhai Xiaodong, Zhang Zhengdong, Chamberlain Robert M, Spitz Margaret R, Wei Qingyi
Department of Epidemiology, The University of Texas M.D. Anderson Cancer Center Houston, TX 77030, USA.
Carcinogenesis. 2006 Oct;27(10):2028-33. doi: 10.1093/carcin/bgl047. Epub 2006 May 4.
The MDM2 protein negatively regulates p53 expression level in modulating DNA repair, cell-cycle control, cell growth and apoptosis. Polymorphisms in the promoter region of the MDM2 gene have been shown to alter protein expression and may, thus, play a role in carcinogenesis. To test our hypothesis that the MDM2 promoter polymorphisms are associated with risk of lung cancer, we conducted a hospital-based, case-control study of 1026 non-Hispanic white patients newly diagnosed with lung cancer and 1145 cancer-free controls who were frequency-matched by age (+/-5 years), sex, ethnicity and smoking status. We genotyped for the MDM2 promoter G2580T (also called SNP309) and G2164A polymorphisms that have a minor allele frequency >0.05. The distributions of the MDM2-2580G variant allele and genotypes were significantly less common among the cases than among the controls (P = 0.038 and 0.045, respectively), but this was not evident for MDM2-2164G (P = 0.865 and 0.614, respectively). Compared with the MDM2-2580TT genotype, the MDM2-2580G variant genotypes were associated with a decreased risk of lung cancer [odds ratio = 0.81 and 95% confidence interval = 0.67-0.98 for GT, 0.83 (0.63-1.08) for GG, and 0.81 (0.68-0.97) for the combined GT/GG genotype]. However, no significant association was observed between the MDM2-2164G variant genotypes and lung cancer risk. Our results suggest that the MDM2-2580G allele may be a marker of reduced genetic susceptibility to lung cancer in the non-Hispanic white population, a finding that seems to contradict previous reports.
MDM2蛋白在调节DNA修复、细胞周期控制、细胞生长和细胞凋亡过程中对p53表达水平起负调控作用。MDM2基因启动子区域的多态性已被证明会改变蛋白表达,因此可能在致癌过程中发挥作用。为了验证我们的假设,即MDM2启动子多态性与肺癌风险相关,我们开展了一项基于医院的病例对照研究,研究对象为1026例新诊断为肺癌的非西班牙裔白人患者以及1145例无癌对照者,这些对照者在年龄(±5岁)、性别、种族和吸烟状况方面进行了频率匹配。我们对MDM2启动子G2580T(也称为SNP309)和G2164A多态性进行基因分型,其次要等位基因频率>0.05。MDM2 - 2580G变异等位基因和基因型的分布在病例组中显著低于对照组(P值分别为0.038和0.045),但MDM2 - 2164G并非如此(P值分别为0.865和0.614)。与MDM2 - 2580TT基因型相比,MDM2 - 2580G变异基因型与肺癌风险降低相关[GT基因型的优势比 = 0.81,95%置信区间 = 0.67 - 0.98;GG基因型为0.83(0.63 - 1.08);GT/GG合并基因型为0.81(0.68 - 0.97)]。然而,未观察到MDM2 - 2164G变异基因型与肺癌风险之间存在显著关联。我们的结果表明,MDM2 - 2580G等位基因可能是非西班牙裔白人人群中肺癌遗传易感性降低的一个标志物,这一发现似乎与先前的报道相矛盾。