Pechlivanis Sonali, Pardini Barbara, Bermejo Justo Lorenzo, Wagner Kerstin, Naccarati Alessio, Vodickova Ludmila, Novotny Jan, Hemminki Kari, Vodicka Pavel, Försti Asta
Division of Molecular Genetic Epidemiology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 580, 69120 Heidelberg, Germany.
Endocr Relat Cancer. 2007 Sep;14(3):733-40. doi: 10.1677/ERC-07-0107.
Western lifestyle leading to obesity and type 2 diabetes has been associated with increased risk of colorectal cancer (CRC). Diet and related factors may affect the risk by modifying plasma insulin levels. Thus, the inter-individual variation in insulin signaling may play a plausible role in the development of CRC. We hypothesized that functional polymorphisms in the insulin pathway genes INS, INSR, IGFBPI, insulin receptor substrate 1 (IRS1), and IRS2 may be associated with CRC. We studied the association of five single nucleotide polymorphisms (SNPs) with the risk of CRC using a hospital-based case-control design with 712 cases and 748 controls from the Czech Republic. The INSR A-603G promoter SNP, which is located within a known Sp1-binding site, was associated with the risk of CRC, with carriers of the G allele having a decreased risk (odds ratios (OR) 0.71, 95% confidence interval (CI) 0.54-0.93). Carrying the variant allele of the IRS1 Gly972Arg SNP further decreased the risk among the INSR-603G allele carriers (OR 0.28, 95% CI 0.11-0.70). SNPs in the INS, IGFBPI, and IRS2 genes did not affect the risk of CRC. In conclusion, genetic variation in the insulin signaling pathway genes may affect the risk of CRC.
西方导致肥胖和2型糖尿病的生活方式与结直肠癌(CRC)风险增加有关。饮食及相关因素可能通过改变血浆胰岛素水平来影响风险。因此,胰岛素信号传导的个体间差异可能在CRC的发生发展中发挥合理作用。我们假设胰岛素途径基因INS、INSR、IGFBPI、胰岛素受体底物1(IRS1)和IRS2中的功能多态性可能与CRC有关。我们采用基于医院的病例对照设计,对来自捷克共和国的712例病例和748例对照进行研究,分析了5个单核苷酸多态性(SNP)与CRC风险的关联。位于已知Sp1结合位点内的INSR A-603G启动子SNP与CRC风险相关,G等位基因携带者风险降低(优势比(OR)0.71,95%置信区间(CI)0.54 - 0.93)。携带IRS1 Gly972Arg SNP的变异等位基因进一步降低了INSR - 603G等位基因携带者的风险(OR 0.28,95% CI 0.11 - 0.70)。INS、IGFBPI和IRS2基因中的SNP不影响CRC风险。总之,胰岛素信号通路基因的遗传变异可能影响CRC风险。