Elingarami Sauli, Liu Hongna, Kalinjuma Aneth Vedastus, Hu Weiyue, Li Song, He Nongyue
J Nanosci Nanotechnol. 2015 Jul;15(7):4815-28. doi: 10.1166/jnn.2015.10028.
China is one of the countries with the highest incidence of gastric cancer, and accounts for over 40% of all new gastric cancer cases in the world. Genetic factors as well as environmental factors play a role in development of gastric cancer. To investigate the independent roles of single nucleotide polymorphisms (SNPs) in base excision repair (BER) genes (APE1 and NEIL2), carcinogen metabolism gene (CYP2E1) and tumor suppressor pathway gene (MDM2) for gastric cancer susceptibility in a Chinese population, we conducted a hospital based case-control study to evaluate the potential association between these polymorphisms and susceptibility to gastric cancer in a Northern Jiangsu population. We also associated the NEIL-2 mRNA expression with the studied NEIL2 SNP genotypes to assess whether the genotypes have influence on the NEIL2 mRNA (hence protein) expression. Five SNPs, APE 1 (rs2275008), NEIL 2 (rs804270), MDM2 (rs2279744), and CYP 2E1 (rs2480256 and rs2031920), were genotyped by TaqMan assays in 105 gastric cancer cases and 118 controls. Genotype frequency distribution showed that the APE 1 SNP (rs2275008), NEIL 2 SNP (rs804270), MDM2 SNP (rs2279744), and CYP 2E1 SNP (rs2031920) had more mutant alleles in gastric cancer cases than controls (76.19, 68.57, 54.29, and 43.81%, respectively), while CYP 2E1 SNP (rs2480256) had large percentage of both alleles (43.81%). Risk analysis revealed that there was increased risk for gastric cancer in subjects with mutant alleles in APE 1 (rs2275008: OR 5.49, 95% CI = 2.6-5.7, p <.0001), NEIL 2 (rs804270: OR 2.3, 95% CI = 1.22-4.3, p=0.01), MDM2 (rs2279744: OR 14.65, 95% CI = 5.63-8.15, p < .0001), and CYP 2E1 (rs2031920: OR 8.385, 95% CI = 3.2-5.3, p < .0001) SNPs. Moreover, the NEIL2 mRNA expression analysis showed that there was significant differential expression of NEIL2 mRNA among the randomly tested NEIL2 genotypes (p = 0.005), with low expression seen in variant genotypes than in other genotypes. In conclusion, variant alleles in the NEIL2 (rs804270), APE1 (rs2275008), CYP2E1 (rs2031920) and MDM2 (rs2279744) SNPs may independently influence susceptibility to gastric cancer in a Northern Jiangsu Chinese population. The genotypes may also independently influence their respective gene mRNA expression, as seen in our study, where there was differential expression of the NEIL2 mRNA among the genotypes, with low NEIL2 mRNA expression seen in the variant genotype.
中国是胃癌发病率最高的国家之一,占全球胃癌新发病例的40%以上。遗传因素和环境因素在胃癌的发生发展中均起作用。为了研究碱基切除修复(BER)基因(APE1和NEIL2)、致癌物代谢基因(CYP2E1)和肿瘤抑制途径基因(MDM2)中的单核苷酸多态性(SNP)在中国人群胃癌易感性中的独立作用,我们进行了一项基于医院的病例对照研究,以评估这些多态性与苏北人群胃癌易感性之间的潜在关联。我们还将NEIL-2 mRNA表达与所研究的NEIL2 SNP基因型相关联,以评估这些基因型是否对NEIL2 mRNA(进而蛋白质)表达有影响。通过TaqMan分析对105例胃癌病例和118例对照进行了5个SNP的基因分型,分别为APE 1(rs2275008)、NEIL 2(rs804270)、MDM(rs2279744)和CYP 2E1(rs2480256和rs2031920)。基因型频率分布显示,APE 1 SNP(rs2275008)、NEIL 2 SNP(rs804270)、MDM2 SNP(rs2279744)和CYP 2E1 SNP(rs2031920)在胃癌病例中的突变等位基因比对照中更多(分别为76.19%、68.57%、54.29%和43.81%),而CYP 2E1 SNP(rs2480256)的两个等位基因比例都很高(43.81%)。风险分析显示,APE 1(rs2275008:OR 5.49,95%CI = 2.6 - 5.7,p <.0001)、NEIL 2(rs804270:OR 2.3,95%CI = 1.22 - 4.3,p = 0.01)、MDM2(rs2279744:OR 14.65,95%CI = 5.63 - 8.15,p <.0001)和CYP 2E1(rs2031920:OR 8.385,95%CI = 3.2 - 5.3,p <.0001)SNP中携带突变等位基因的受试者患胃癌的风险增加。此外,NEIL2 mRNA表达分析显示,在随机检测的NEIL2基因型中,NEIL2 mRNA存在显著差异表达(p = 0.005),变异基因型中的表达低于其他基因型。总之,NEIL2(rs804270)、APE1(rs2275008)、CYP2E1(rs2031920)和MDM2(rs2279744)SNP中的变异等位基因可能独立影响苏北中国人群的胃癌易感性。如我们的研究所示,这些基因型也可能独立影响其各自基因的mRNA表达,其中NEIL2 mRNA在基因型间存在差异表达,变异基因型中NEIL2 mRNA表达较低。