Pan Xiong-Fei, Yang Shu-Juan, Loh Marie, Xie Yao, Wen Yuan-Yuan, Tian Zhi, Huang He, Lan Hui, Chen Feng, Soong Richie, Yang Chun-Xia
Department of Epidemiology, West China School of Public Health, Sichuan University, Chengdu, Sichuan, China.
Asian Pac J Cancer Prev. 2013;14(4):2577-82. doi: 10.7314/apjcp.2013.14.4.2577.
Interleukin (IL) -10 is a potent cytokine with a dual ability to immunosuppress or immunostimulate. We aimed to explore the association of IL10 promoter polymorphisms with risk of gastric cancer (GC) in a Han population in Southwestern China.
We enrolled 308 pairs of GC and control subjects from four hospitals and a community between October 2010 and August 2011 in a 1:1 matched case-control design. Demographic information was collected using a designed questionnaire. IL10-592 A>C and IL10-1082 A>G polymorphisms were determined by Sequenom MassARRAY analysis.
Patients with GC reported statistically higher proportions of family history of cancer (29.9% versus 10.7%, P<0.01) and alcohol drinking (54.6% versus 43.2%, P<0.01) than did controls. Similar results were observed in comparison between non-cardia GC patients and controls (P<0.01 and P=0.03). Variant genotypes of IL10-592 A>C and IL10-1082 A>G were not associated with overall GC risk (adjusted OR, 0.94, 95% CI, 0.66-1.33; adjusted OR, 1.00, 95% CI, 0.62-1.60). Sub-analysis showed that the IL10-592 AC/CC variant genotype was associated with decreased non-cardia GC risk (adjusted OR, 0.58; 95% CI, 0.36-0.95). No association was found between any of the IL10 haplotypes established from two polymorphisms and risk of non-cardia GC.
In conclusion, our data do not link the two SNPs of IL10-592 and IL10-1082 with overall GC risk. We demonstrate that IL10-592 polymorphism is associated with protective effect against non-cardia GC. Our findings may offer insight into risk associated with the development of GC in this region.
白细胞介素(IL)-10是一种具有免疫抑制或免疫刺激双重能力的强效细胞因子。我们旨在探讨中国西南地区汉族人群中IL10启动子多态性与胃癌(GC)风险的关联。
在2010年10月至2011年8月期间,我们采用1:1匹配的病例对照设计,从四家医院和一个社区招募了308对GC患者和对照受试者。使用设计好的问卷收集人口统计学信息。通过Sequenom MassARRAY分析确定IL10 -592 A>C和IL10 -1082 A>G多态性。
与对照组相比,GC患者报告的癌症家族史比例(29.9%对10.7%,P<0.01)和饮酒比例(54.6%对43.2%,P<0.01)在统计学上更高。在非贲门GC患者与对照组的比较中也观察到了类似结果(P<0.01和P = 0.03)。IL10 -592 A>C和IL10 -1082 A>G的变异基因型与总体GC风险无关(校正OR,0.94,95%CI,0.66 - 1.33;校正OR,1.00,95%CI,0.62 - 1.60)。亚分析表明,IL10 -592 AC/CC变异基因型与非贲门GC风险降低相关(校正OR,0.58;95%CI,0.36 - 0.95)。从两个多态性建立的任何IL10单倍型与非贲门GC风险之间均未发现关联。
总之,我们的数据并未将IL10 -592和IL10 -1082的两个单核苷酸多态性与总体GC风险联系起来。我们证明IL10 -592多态性与非贲门GC的保护作用相关。我们的研究结果可能为该地区GC发生的相关风险提供见解。