Zhou Cheng-Jiang, Zhang Liu-Wei, Gao Fang, Zhang Bin, Wang Ying, Chen Da-Fang, Jia Yan-Bin
School of Basic Medicine, Baotou Medical College, Baotou, China E-mail :
Asian Pac J Cancer Prev. 2014;15(10):4207-10. doi: 10.7314/apjcp.2014.15.10.4207.
Several lines of evidence suggest that genetic variation in MUC5AC gene might contribute to the risk of gastric cancer. We conducted a case-control study to evaluate the relationship between common genetic variations in MUC5AC gene and non-cardia gastric cancer using an LD-based tagSNP approach in Baotou, north-western China. We genotyped 12 tagSNPs by TaqMan method among 288 cases with non-cardia gastric cancer and 281 normal controls. Unconditional logistic regression was used to calculate odds ratios (ORs) and 95% confidence intervals (CIs) for non-cardia gastric cancer risk in association with alleles, genotypes and haplotypes. We observed that the frequencies of rs3793964 C allele and rs11040869 A allele were significantly lower in cases than in controls. Meanwhile, minor allele homozygotes of rs3793964 and rs11040869 were significantly associated with a decreased risk of non-cardia gastric cancer when compared with their major allele homozygotes. Furthermore, a statistically significantly protective effect of rs885454 genotypes on non-cardia gastric cancer was also observed (for CT vs. CC: OR=0.581, 95%CI=0.408-0.829; for CT/TT vs. CC: OR=0.623, 95%CI=0.451-0.884). Our results indicated that some common genetic variations in the MUC5AC gene might have effects on the risk of non-cardia gastric cancer in our studied population.
多条证据表明,MUC5AC基因的遗传变异可能会增加患胃癌的风险。我们在中国西北部的包头进行了一项病例对照研究,采用基于连锁不平衡的标签单核苷酸多态性(tagSNP)方法,评估MUC5AC基因常见遗传变异与非贲门胃癌之间的关系。我们采用TaqMan方法对288例非贲门胃癌患者和281名正常对照进行了12个标签单核苷酸多态性的基因分型。采用非条件逻辑回归计算等位基因、基因型和单倍型与非贲门胃癌风险相关的比值比(OR)和95%置信区间(CI)。我们观察到,病例组中rs3793964 C等位基因和rs11040869 A等位基因的频率显著低于对照组。同时,与主要等位基因纯合子相比,rs3793964和rs11040869的次要等位基因纯合子与非贲门胃癌风险降低显著相关。此外,还观察到rs885454基因型对非贲门胃癌具有统计学显著的保护作用(CT与CC相比:OR = 0.581,95%CI = 0.408 - 0.829;CT/TT与CC相比:OR = 0.623,95%CI = 0.451 - 0.884)。我们的结果表明,MUC5AC基因的一些常见遗传变异可能会影响我们研究人群中非贲门胃癌的风险。