Su Qinghua, Wang Yuan, Zhao Jun, Ma Cangjian, Wu Tao, Jin Tianbo, Xu Jinkai
Department of General Surgery, the Second Affiliated Hospital, Xi'an Jiaotong University School of Medicine, No. 157 West Fifth Road, Xi'an, Shaanxi, 710004, China.
Inner Mongolia Medical University, Hohhot, Inner Mongolia, 010010, China.
BMC Gastroenterol. 2015 Aug 25;15:107. doi: 10.1186/s12876-015-0336-9.
Gastric and colorectal cancers have a major impact on public health, and are the most common malignant tumors in China. The aim of this research was to study whether polymorphisms of CHCHD3P1-HSP90AB7P, GRID1, HSPA12A, PRLHR, SBF2, POLD3 and C11orf93-C11orf92 genes are associated with the risk of gastric and colorectal cancers in the Chinese Han population.
We genotyped seven single nucleotide polymorphisms (SNPs) from seven genes. We selected 588 patients with gastric cancer and 449 with colorectal cancer, along with 703 healthy controls. All these SNPs were evaluated using the χ² test and genetic model analysis.
The genotype "A/T" of rs12413624 in PRLHR gene was associated with a decreased risk of colorectal cancer in allele model analysis [odds ratio (OR) = 0.81; 95% confidence interval (CI) = 0.68-0.97; p = 0.018] and log-additive model analysis (OR = 0.81; 95% CI = 0.66-0.98; p = 0.032). The genotype "A/G" of rs1665650 in HSPA12A gene was associated with a decreased risk of gastric cancer in overdominant model analysis (OR = 0.77; 95% CI = 0.60-0.99; p = 0.038).
Our results provide evidence that variants of PRLHR gene are a protective factor in colorectal cancer and variants of HSPA12A gene are a protective factor in gastric cancer in the Chinese Han population.
胃癌和结直肠癌对公众健康有重大影响,是中国最常见的恶性肿瘤。本研究的目的是探讨CHCHD3P1-HSP90AB7P、GRID1、HSPA12A、PRLHR、SBF2、POLD3和C11orf93-C11orf92基因的多态性是否与中国汉族人群患胃癌和结直肠癌的风险相关。
我们对7个基因的7个单核苷酸多态性(SNP)进行了基因分型。我们选取了588例胃癌患者和449例结直肠癌患者,以及703名健康对照。所有这些SNP均使用χ²检验和遗传模型分析进行评估。
PRLHR基因中rs12413624的基因型“A/T”在等位基因模型分析中与结直肠癌风险降低相关[比值比(OR)=0.81;95%置信区间(CI)=0.68-0.97;p=0.018],在对数加性模型分析中(OR=0.81;95%CI=0.66-0.98;p=0.032)。HSPA12A基因中rs1665650的基因型“A/G”在超显性模型分析中与胃癌风险降低相关(OR=0.77;95%CI=0.60-0.99;p=0.038)。
我们的结果表明,PRLHR基因变异是中国汉族人群结直肠癌的保护因素,HSPA12A基因变异是中国汉族人群胃癌的保护因素。