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白细胞介素-6基因启动子-174G/C单核苷酸多态性与克什米尔族人群结直肠癌风险降低的强关联:一项病例对照研究

Strong association of interleukin-6 -174G/C promoter single nucleotide polymorphism with a decreased risk of colorectal cancer in ethnic Kashmiri population: A case control study.

作者信息

Banday Mujeeb Zafar, Balkhi Henah Mehraj, Sameer Aga Syed, Chowdri Nissar A, Haq Ehtishamul

机构信息

1 Department of Biotechnology, University of Kashmir, Srinagar, India.

2 Department of Basic Medical Sciences, College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Jeddah, Kingdom of Saudi Arabia.

出版信息

Tumour Biol. 2017 Mar;39(3):1010428317695940. doi: 10.1177/1010428317695940.

Abstract

Chronic inflammation increases the risk of development of various cancers, including colorectal cancer. Interleukin-6 has been described as a key regulator of colorectal cancer development and is important in the process of colorectal tumorigenesis largely through the regulation of tumor-promoting inflammation. Several studies have reported the association of various polymorphisms in human interleukin-6 gene including IL-6 -174G/C single nucleotide polymorphism with various cancers, including colorectal cancer, but the results are mixed and inconclusive. The aim of this study was to analyze the association of IL-6 -174G/C promoter single nucleotide polymorphism with colorectal cancer risk and also to evaluate the modifying effects of possible IL-6 -174G/C single nucleotide polymorphism genotypes on different risk factors of colorectal cancer or the reciprocal effect in ethnic Kashmiri population through a case control setup. The genotype frequencies of IL-6 -174G/C promoter single nucleotide polymorphism were compared between 142 colorectal cancer patients and 184 individually matched healthy controls by using polymerase chain reaction-restriction fragment length polymorphism method. The association between the IL-6 -174G/C single nucleotide polymorphism and colorectal cancer risk was examined through conditional logistic regression models adjusted for multiple possible confounding (third) variables. The possible effect measure modification of the association between the relevant single nucleotide polymorphism genotypes and colorectal cancer risk by various colorectal cancer risk factors including age, gender, and smoking status was also evaluated. Furthermore, the associations between these single nucleotide polymorphisms and various clinicopathological parameters, demographic variables, and environmental factors within the case group subjects with regard to colorectal cancer risk were also analyzed. The overall association between the IL-6 -174G/C single nucleotide polymorphism and the modulation of colorectal cancer risk was found to be highly significant (p = 0.001). The variant genotype (CC) was significantly associated with a decreased risk of colorectal cancer (odds ratio, 0.15 (95% confidence interval, 0.04-0.54); p = 0.004). Furthermore, the less common IL-6-174C allele was associated with a decreased risk of colorectal cancer (odds ratio, 0.49 (95% confidence interval, 0.33-0.73); p = 0.0006). The combined variant genotype (GC + CC) was also significantly associated with a decreased risk of colorectal cancer (odds ratio, 0.54 (95% confidence interval, 0.33-0.89); p = 0.015). This study demonstrates that there is a strong and highly significant association between the IL-6 -174G/C promoter single nucleotide polymorphism and a decreased risk of colorectal cancer in ethnic Kashmiri population. However, in order to substantiate our findings, this study needs to be replicated with larger sample size and with other ethnically defined populations with comparable colorectal cancer incidence.

摘要

慢性炎症会增加包括结直肠癌在内的各种癌症发生的风险。白细胞介素-6被认为是结直肠癌发生发展的关键调节因子,在结直肠癌的发生过程中起着重要作用,主要是通过调节促肿瘤炎症来实现的。多项研究报道了人类白细胞介素-6基因中的各种多态性,包括IL-6 -174G/C单核苷酸多态性与包括结直肠癌在内的各种癌症之间的关联,但结果不一且尚无定论。本研究的目的是分析IL-6 -174G/C启动子单核苷酸多态性与结直肠癌风险之间的关联,并通过病例对照研究评估IL-6 -174G/C单核苷酸多态性可能的基因型对结直肠癌不同危险因素的修饰作用或相互作用,研究对象为克什米尔族人群。采用聚合酶链反应-限制性片段长度多态性方法,比较了142例结直肠癌患者和184例个体匹配的健康对照者中IL-6 -174G/C启动子单核苷酸多态性的基因型频率。通过对多个可能的混杂(第三)变量进行校正的条件逻辑回归模型,检验IL-6 -174G/C单核苷酸多态性与结直肠癌风险之间的关联。还评估了包括年龄、性别和吸烟状况在内的各种结直肠癌危险因素对相关单核苷酸多态性基因型与结直肠癌风险之间关联的可能效应修饰。此外,还分析了这些单核苷酸多态性与病例组中结直肠癌风险相关的各种临床病理参数、人口统计学变量和环境因素之间的关联。发现IL-6 -174G/C单核苷酸多态性与结直肠癌风险的调节之间存在高度显著的总体关联(p = 0.001)。变异基因型(CC)与结直肠癌风险降低显著相关(优势比,0.15(95%置信区间,0.04 - 0.54);p = 0.004)。此外,较罕见的IL-6-174C等位基因与结直肠癌风险降低相关(优势比,0.49(95%置信区间,0.33 - 0.73);p = 0.0006)。联合变异基因型(GC + CC)也与结直肠癌风险降低显著相关(优势比,0.54(95%置信区间,0.33 - 0.89);p = 0.015)。本研究表明,在克什米尔族人群中,IL-6 -174G/C启动子单核苷酸多态性与结直肠癌风险降低之间存在强烈且高度显著的关联。然而,为了证实我们的发现,本研究需要在更大样本量以及其他结直肠癌发病率相当的不同种族定义人群中进行重复验证。

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