Mittelstrass Kirstin, Sauter Wiebke, Rosenberger Albert, Illig Thomas, Timofeeva Maria, Klopp Norman, Dienemann Hendrik, Meese Eckart, Sybrecht Gerhard, Woelke Gabi, Cebulla Mathias, Degen Maria, Morr Harald, Drings Peter, Groeschel Andreas, Kreymborg Karsten Grosse, Haeussinger Karl, Hoeffken Gerd, Schmidt Christine, Jilge Bettina, Schmidt Wilhelm, Ko You-Dschun, Taeuscher Dagmar, Chang-Claude Jenny, Wichmann Heinz-Erich, Bickeboeller Heike, Risch Angela
Helmholtz Center Munich, German Research Center for Environmental Health, Institute of Epidemiology, Munich/Neuherberg, Germany.
BMC Cancer. 2008 Apr 23;8:113. doi: 10.1186/1471-2407-8-113.
The polymorphism SNP309 (rs2279744) in the promoter region of the MDM2 gene has been shown to alter protein expression and may play a role in the susceptibility to lung cancer. The MDM2 protein is a key inhibitor of p53 and several mechanisms of MDM2/p53 interactions are presently known: modulating DNA-repair, cell-cycle control, cell growth and apoptosis.We used 635 Caucasian patients diagnosed with lung cancer before 51 years of age and 1300 healthy gender and age frequency matched population Caucasian controls to investigate the association between the MDM2 SNP309 and the risk of developing early onset lung cancer. Conditional logistic models were applied to assess the genotype-phenotype association, adjusted for smoking. Compared to the GG genotype, the adjusted ORs for the TG and TT genotype were 0.9 (95% CI: 0.7-1.5) and 1.0 (95% CI: 0.7-1.5), respectively. Also no association was found for histological subtypes of lung cancer. The strength of this study is that within young cases the genetic component to develop lung cancer may be greater. Our results indicate that the MDM2 SNP309 is not significantly associated with lung carcinogenesis but point towards gender-specific differences.
MDM2基因启动子区域的多态性SNP309(rs2279744)已被证明会改变蛋白质表达,并可能在肺癌易感性中发挥作用。MDM2蛋白是p53的关键抑制剂,目前已知MDM2/p53相互作用的几种机制:调节DNA修复、细胞周期控制、细胞生长和细胞凋亡。我们使用了635名51岁之前被诊断为肺癌的白种人患者以及1300名年龄和性别频率匹配的健康白种人对照,以研究MDM2 SNP309与早发性肺癌发病风险之间的关联。应用条件逻辑模型来评估基因型与表型的关联,并对吸烟因素进行了校正。与GG基因型相比,TG和TT基因型的校正比值比分别为0.9(95%置信区间:0.7 - 1.5)和1.0(95%置信区间:0.7 - 1.5)。在肺癌组织学亚型方面也未发现关联。本研究的优势在于,在年轻病例中,肺癌发生的遗传因素可能更大。我们的结果表明,MDM2 SNP309与肺癌发生没有显著关联,但存在性别特异性差异。