Wu Chen, Wang Guanghai, Yang Ming, Huang Liming, Yu Dianke, Tan Wen, Lin Dongxin
Bejing Key Laboratory of Cancer Prevention, Cancer Institute and Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Mol Carcinog. 2009 Dec;48(12):1131-8. doi: 10.1002/mc.20565.
Genetic factors play important roles in pathogenesis of human cancer. A recent genome-wide association study (GWAS) linked two single nucleotide polymorphisms (SNPs) in prostate stem cell antigen (PSCA), rs2294008C>T and rs2976392G>A, to risk of diffuse-type of gastric cancer in Japanese and Korean populations. We hypothesized that these two SNPs are also associated with risk of gastric cancer in Chinese population. We examined genotypes and haplotypes of PSCA, rs2294008C/T and rs2976392G/A in 716 patients with cardia gastric carcinoma (CGC), 1020 patients with noncardia gastric carcinoma (NCGC), and 1020 controls. We found that individuals with at least one copy of the rs2294008T allele (CT or TT genotype) had an elevated risk for developing NCGC compared with those without this allele (OR = 1.35, 95% CI = 1.13-1.61). Individuals with at least one copy of the rs2976392A allele (GA or AA genotype) had nonsignificantly increased risk for NCGC compared with those without this allele (OR = 1.20, 95% CI = 1.01-1.43). Stratification analysis showed that the increased risk associated with the SNPs was restricted in female subjects. Moreover, the rs2294008T and rs2976392A allele carriers were predisposed to developing poorly differentiated and high stage NCGC at diagnosis. However, no such association was detected for CGC. In addition, we observed considerably lower allelic and genotype frequencies of these genetic variants in Chinese population compared with Japanese and Korean populations. These findings are in general consistent with previous GWAS and suggest that PSCA may play a role in the development of NCGC in Chinese population.
遗传因素在人类癌症的发病机制中起着重要作用。最近一项全基因组关联研究(GWAS)将前列腺干细胞抗原(PSCA)中的两个单核苷酸多态性(SNP),即rs2294008C>T和rs2976392G>A,与日本和韩国人群中弥漫型胃癌的风险联系起来。我们假设这两个SNP也与中国人群胃癌风险相关。我们检测了716例贲门胃癌(CGC)患者、1020例非贲门胃癌(NCGC)患者和1020例对照中PSCA的rs2294008C/T和rs2976392G/A的基因型和单倍型。我们发现,与没有该等位基因的个体相比,至少有一个rs2294008T等位基因拷贝(CT或TT基因型)的个体患NCGC的风险升高(OR = 1.35,95%CI = 1.13 - 1.61)。与没有该等位基因的个体相比,至少有一个rs2976392A等位基因拷贝(GA或AA基因型)的个体患NCGC的风险非显著增加(OR = 1.20,95%CI = 1.01 - 1.43)。分层分析表明,与这些SNP相关的风险增加仅限于女性受试者。此外,rs2294008T和rs2976392A等位基因携带者在诊断时易患低分化和高分期的NCGC。然而,在CGC中未检测到这种关联。此外,与日本和韩国人群相比,我们观察到中国人群中这些遗传变异的等位基因和基因型频率显著较低。这些发现总体上与之前的GWAS一致,并表明PSCA可能在中国人群NCGC的发生中起作用。