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微粒体环氧化物水解酶基因 Tyr113His 和 His139Arg 活性改变基因型与食管鳞癌的相关性。

Association of Activity Altering Genotypes - Tyr113His and His139Arg in Microsomal Epoxide Hydrolase Enzyme with Esophageal Squamous Cell Carcinoma.

机构信息

a Department of Biochemistry , University of Kashmir , Srinagar , J&K , India.

b Department of Radiation Oncology , SK Institute of Medical Sciences , Srinagar , J&K , India.

出版信息

Nutr Cancer. 2019;71(5):806-817. doi: 10.1080/01635581.2018.1484934. Epub 2019 Jan 11.

Abstract

The study aimed to explore the relationship of microsomal epoxide hydrolase (mEH) exon 3 (Tyr113His) and exon 4 (His139Arg) polymorphisms and predicted mEH activity with esophageal squamous cell carcinoma (ESCC) risk. 482 histologically confirmed cases and equal number of matched controls were analyzed by polymerase chain reaction-restriction length polymorphism (PCR-RFLP). Conditional logistic regression models were used to examine the association of polymorphisms with ESCC. We noted exon 3 slow genotype (OR = 6.57; CI 3.43-12.57) as well as predicted low mEH activity (OR = 3.99; CI 2.32-6.85) was associated with the ESCC risk. Elevated ESCC risk estimates were seen in smokers independent of genotypes but the association was stronger among smokers with exon 3 variant (OR = 6.67; 3.29-13.53) and low activity (OR = 7.52; CI 3.46-16.37) genotypes. Positive family history of cancer synergistically increased ESCC risk in the individuals who harbored exon 3 (OR = 13.59; CI 5.63-32.81) or altered mEH activity genotypes (OR = 13.35; CI 5.10-34.94). Significant interaction was seen between mEH exon 3 and exon 4 genotypes (P = 0.006) and between predicted mEH activity and positive family history of cancer (P = 0.018). These findings suggest association of ESCC risk with mEH polymorphisms which get modified by tobacco smoking and positive family history of cancer.

摘要

本研究旨在探讨细胞色素 P450 2E1(CYP2E1)基因多态性与食管癌易感性的关系。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法对 482 例经组织学证实的食管癌患者和 482 例匹配的对照进行分析。采用条件 logistic 回归模型分析多态性与食管癌的关系。我们发现,exon 3 慢代谢基因型(OR=6.57;95%CI:3.43-12.57)和预测的低 mEH 活性(OR=3.99;95%CI:2.32-6.85)与食管癌的发病风险相关。在不考虑基因型的情况下,我们发现吸烟者食管癌发病风险升高,但这种相关性在携带 exon 3 变异(OR=6.67;95%CI:3.29-13.53)和低活性(OR=7.52;95%CI:3.46-16.37)基因型的吸烟者中更强。有癌症阳性家族史的个体,携带 exon 3 或改变 mEH 活性的基因型,食管癌发病风险协同增加(OR=13.59;95%CI:5.63-32.81;OR=13.35;95%CI:5.10-34.94)。我们还观察到 mEH exon 3 和 exon 4 基因型(P=0.006)以及预测的 mEH 活性和阳性家族史(P=0.018)之间存在显著的交互作用。这些结果提示 mEH 多态性与食管癌风险相关,这种相关性受到吸烟和阳性家族史的影响。

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