中国白族人群CTLA-4多态性与胃癌风险的相关性

IF 2.3 4区 医学 Q3 GENETICS & HEREDITY
Ping Yan, Shan Kong, Yong Zheng, Mingjing Cheng, Weidong Zhao
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引用次数: 0

摘要

细胞毒性T淋巴细胞相关抗原-4 (CTLA-4)参与调节T细胞介导的免疫反应。本研究旨在探讨CTLA-4基因多态性与中国西南白族人群胃癌(GC)发病风险的关系。本病例对照研究共纳入422例胃癌患者和397例健康对照。选择CTLA-4基因的4个单核苷酸多态性位点(rs231775、rs733618、rs16840252和rs3087243)进行分析。结果显示,rs733618位点在GC组和HC组之间存在显著差异。与HC组相比,GC组rs733618多态性“TC”基因型的频率显著降低[优势比(OR), 95%可信区间(CI): 0.47 (0.35 - 0.63), p <措施)。显性遗传模式为“TC + CC”的胃癌患者发生胃癌的风险降低47% [OR, 95%CI: 0.53 (0.40 - 0.71), p <措施)。亚组分析显示,rs733618“TC + CC”基因型与男性患者较低的GC风险相关[OR, 95%CI: 0.42 (0.31 - 0.58), p <.001],年龄≤60岁者[OR, 95%CI: 0.27 (0.18 - 0.42), p <措施,不喝酒(或者,95%置信区间ci: .21 (13 .33), p & lt;措施),非吸烟者(或者,95%置信区间ci: 38 (.25 .57), p & lt;.001]和未感染幽门螺杆菌的个体[OR, 95%CI: 0.16 (0.10 - 0.26), p <措施)。进一步的多变量分析表明,年龄≤60岁[OR, 95%CI: 0.42 (0.29 - 0.83), p = 0.032]且未感染幽门螺杆菌[OR, 95%CI: 0.35 (0.28 - 0.76), p = 0.018]的“TC + CC”rs733618基因型个体对胃癌具有保护作用。此外,可溶性CTLA-4在“TC”和“TC + CC”基因型的GC患者中显著降低(p <.05). 我们的研究结果提示CTLA-4基因rs733618多态性可能在GC的预防中起关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Correlation of CTLA-4 polymorphism and the risk of gastric cancer in a Chinese Bai population

Cytotoxic T lymphocyte-associated antigen-4 (CTLA-4) is involved in the regulation of immune responses mediated by T cells. This study aimed to explore the correlation between CTLA-4 gene polymorphisms and the risk of gastric cancer (GC) in the Bai minority population of southwestern China. A total of 422 GC patients and 397 healthy controls (HC) were included in this case–control study. Four single nucleotide polymorphism sites of CTLA-4 gene (rs231775, rs733618, rs16840252 and rs3087243) were selected and analysed. The results showed a significant difference in the rs733618 loci between GC and HC groups. The frequency of the rs733618 polymorphism ‘TC’ genotype was significantly lower in GC group compared to the HC group [odds ratio (OR), 95% confidence interval (CI): .47 (.35–.63), p < .001]. GC cases with dominant genetic model ‘TC + CC’ had a 47% reduced risk of GC [OR, 95%CI: .53 (.40–.71), p < .001]. Subgroup analyses revealed that the rs733618 ‘TC + CC’ genotype was associated with a lower risk of GC in male patients [OR, 95%CI: .42 (.31–.58), p < .001], those aged ≤60 years old [OR, 95%CI: .27 (.18–.42), p < .001], non-drinkers [OR, 95%CI: .21 (.13–.33), p < .001], non-smokers [OR, 95%CI: .38 (.25–.57), p < .001] and individuals without Helicobacter pylori infection [OR, 95%CI: .16 (.10–.26), p < .001]. Further multivariated analyses indicated that individuals with the ‘TC + CC’ rs733618 genotype who were aged ≤60 years old [OR, 95%CI: .42 (.29–.83), p = .032] and had no H. pylori infection [OR, 95%CI: .35 (.28–.76), p = .018] were found to have a protective effect against GC. Additionally, soluble CTLA-4 were significantly lower in GC patients with ‘TC’ and ‘TC + CC’ genotypes (all p < .05). Our findings suggest that the rs733618 polymorphism of CTLA-4 gene may play a critical role in the prevention of GC.

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来源期刊
CiteScore
4.70
自引率
0.00%
发文量
48
审稿时长
6-12 weeks
期刊介绍: The International Journal of Immunogenetics (formerly European Journal of Immunogenetics) publishes original contributions on the genetic control of components of the immune system and their interactions in both humans and experimental animals. The term ''genetic'' is taken in its broadest sense to include studies at the evolutionary, molecular, chromosomal functional and population levels in both health and disease. Examples are: -studies of blood groups and other surface antigens- cell interactions and immune response- receptors, antibodies, complement components and cytokines- polymorphism- evolution of the organisation, control and function of immune system components- anthropology and disease associations- the genetics of immune-related disease: allergy, autoimmunity, immunodeficiency and other immune pathologies- All papers are seen by at least two independent referees and only papers of the highest quality are accepted.
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