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白细胞介素-10 多态性、幽门螺杆菌感染和吸烟对非贲门胃癌发病风险的影响。

Effects of interleukin-10 polymorphisms, Helicobacter pylori infection, and smoking on the risk of noncardia gastric cancer.

机构信息

Cancer Epidemiology Branch, National Cancer Center, Goyang, Korea.

出版信息

PLoS One. 2012;7(1):e29643. doi: 10.1371/journal.pone.0029643. Epub 2012 Jan 3.

Abstract

OBJECTIVE

Both variations in the interleukin-10 (IL10) gene and environmental factors are thought to influence inflammation and gastric carcinogenesis. Therefore, we investigated the associations between IL10 polymorphisms, Helicobacter pylori (H. pylori) infection, and smoking in noncardia gastric carcinogenesis in Koreans.

METHODS

We genotyped three promoter polymorphisms (-1082A>G, -819T>C, and -592 A>C) of IL10 in a case-control study of 495 noncardia gastric cancer patients and 495 sex- and age-matched healthy controls. Multiple logistic regression models were used to detect the effects of IL10 polymorphisms, H. pylori infection, and smoking on the risk of gastric cancer, which was stratified by the histological type of gastric cancer.

RESULTS

The IL10-819C and -592C alleles were found to have complete linkage disequilibrium, and all three IL10 polymorphisms were associated with an increased risk of intestinal-type noncardia gastric cancer. These associations were observed only in H. pylori-positive subjects and current smokers. A statistically significant interaction between the IL10-592 genotype and H. pylori infection on the risk of intestinal-type gastric cancer was observed (P for interaction  = 0.047). In addition, H. pylori-positive smokers who were carriers of either the IL10-1082G (OR [95% CI]  = 17.76 [6.17-51.06]) or the -592C (OR [95% CI]  = 8.37 [2.79-25.16]) allele had an increased risk of intestinal-type gastric cancer compared to H. pylori-negative nonsmokers homozygous for IL10-1082A and -592A, respectively. The interaction between the IL10-1082 polymorphism and the combined effects of H. pylori infection and smoking tended towards significance (P for interaction  = 0.080).

CONCLUSIONS

Inflammation-related genetic variants may interact with H. pylori infection and smoking to increase the risk of noncardia gastric cancer, particularly the intestinal-type. These findings may be helpful in identifying individuals at an increased risk for developing noncardia gastric cancer.

摘要

目的

白细胞介素-10(IL10)基因的变异和环境因素都被认为会影响炎症和胃癌的发生。因此,我们研究了白细胞介素-10 多态性、幽门螺杆菌(H. pylori)感染和吸烟与韩国非贲门胃癌发生的关系。

方法

我们在一项病例对照研究中对 495 例非贲门胃癌患者和 495 例性别和年龄匹配的健康对照者进行了白细胞介素-10 启动子-1082A>G、-819T>C 和-592A>C 三个多态性的基因分型。采用多因素逻辑回归模型检测白细胞介素-10 多态性、H. pylori 感染和吸烟对胃癌风险的影响,并按胃癌组织学类型进行分层。

结果

IL10-819C 和 -592C 等位基因完全连锁不平衡,所有三种白细胞介素-10 多态性均与肠型非贲门胃癌的发病风险增加相关。这些关联仅见于 H. pylori 阳性者和现吸烟者。IL10-592 基因型与 H. pylori 感染对肠型胃癌发病风险的交互作用具有统计学意义(交互作用 P 值=0.047)。此外,H. pylori 阳性吸烟者中,无论携带 IL10-1082G(OR[95%CI]为 17.76[6.17-51.06])或-592C(OR[95%CI]为 8.37[2.79-25.16])等位基因,其患肠型胃癌的风险均高于 H. pylori 阴性且白细胞介素-10-1082A 和 -592A 均为纯合子的非吸烟者。IL10-1082 多态性与 H. pylori 感染和吸烟联合作用的交互作用有统计学意义(交互作用 P 值=0.080)。

结论

与炎症相关的遗传变异可能与 H. pylori 感染和吸烟相互作用,增加非贲门胃癌的发病风险,尤其是肠型。这些发现可能有助于识别发生非贲门胃癌风险增加的个体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a445/3250465/5e7fc58f256c/pone.0029643.g001.jpg

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