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T 细胞免疫球蛋白和黏蛋白结构域分子 3 基因多态性与胰腺癌易感性。

T cell immunoglobulin- and mucin-domain-containing molecule 3 gene polymorphisms and susceptibility to pancreatic cancer.

机构信息

Department of Surgery, The Sixth People's Hospital, Shanghai Jiao Tong University, Shanghai 200233, China.

出版信息

Mol Biol Rep. 2012 Nov;39(11):9941-6. doi: 10.1007/s11033-012-1862-y. Epub 2012 Jun 26.

Abstract

T cell immunoglobulin- and mucin-domain-containing molecule 3 (TIM-3) is a novel transmembrane protein that is involved in the regulation of T-helper 1 cell-mediated immunity. Studies have shown that polymorphisms in TIM-3 gene can be associated with various diseases. Here, we investigated the correlation of TIM-3 polymorphisms with susceptibility to pancreatic cancer in the Chinese population. Three polymorphisms in TIM-3 gene (-1516G/T, -574G/T, and +4259T/G) were identified by polymerase chain reaction-restriction fragment length polymorphism in 306 pancreatic patients and 408 healthy controls. Results showed that the prevalence of +4259TG genotype and +4259G allele were significantly increased in the pancreatic cancer cases than in controls [odds ratio (OR) = 2.82, 95 % confidence interval (CI), 1.45-5.48, p = 0.0015, and OR = 2.74, 95 % CI, 1.42-2.94, p = 0.0017]. In addition, when analyzing the TIM-3 polymorphisms with different clinical parameters in pancreatic cancer patients, the cases with vascular infiltration had higher numbers of +4259T/G polymorphism than those without vascular infiltration (OR = 3.07, 95 % CI, 1.41-6.68, p = 0.003). These results suggested polymorphisms in TIM-3 gene could be new risk factors for the development of pancreatic cancer.

摘要

T 细胞免疫球蛋白和粘蛋白结构域蛋白 3(TIM-3)是一种新型的跨膜蛋白,参与调节辅助性 T 细胞介导的免疫。研究表明,TIM-3 基因多态性与多种疾病相关。在这里,我们研究了 TIM-3 基因多态性与中国人群胰腺癌易感性的相关性。通过聚合酶链反应-限制性片段长度多态性在 306 例胰腺癌患者和 408 例健康对照中鉴定出 TIM-3 基因的三个多态性(-1516G/T、-574G/T 和+4259T/G)。结果显示,胰腺癌病例中+4259TG 基因型和+4259G 等位基因的患病率明显高于对照组[比值比(OR)=2.82,95%置信区间(CI)1.45-5.48,p=0.0015 和 OR=2.74,95%CI,1.42-2.94,p=0.0017]。此外,在分析胰腺癌患者不同临床参数的 TIM-3 多态性时,有血管浸润的病例+4259T/G 多态性的数量高于无血管浸润的病例(OR=3.07,95%CI,1.41-6.68,p=0.003)。这些结果表明 TIM-3 基因多态性可能是胰腺癌发生的新危险因素。

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