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白细胞介素-18(-607 C/A)和白细胞介素-18(-137 G/C)基因变异在膀胱癌发展中的作用研究:病例对照研究。

Investigation of the roles of IL-18 (-607 C/A) and IL-18 (-137 G/C) gene variations in bladder cancer development: case-control study.

机构信息

Department of Biophysics, Faculty of Medicine, Haliç University, Istanbul, 34445, Turkey.

Department of Biophysics, Faculty of Medicine, Trakya University, Edirne, 22030, Turkey.

出版信息

J Cancer Res Clin Oncol. 2021 Dec;147(12):3627-3637. doi: 10.1007/s00432-021-03808-y. Epub 2021 Sep 22.

Abstract

BACKGROUND

The purpose of our study is to investigate the roles of IL-18 gene variations in bladder cancer development in Thrace population of Turkey.

METHODS

This study was carried out with 103 bladder cancer patients and 81 healthy controls. Genotype distributions of IL-18 (-137 G/C) and IL-18 (-607 C/A) gene variations were determined using polymerase chain reaction (PCR) method.

RESULTS

The CC homozygous genotype for IL-18 (-607 C/A) gene variation was significantly higher in patients with bladder cancer compared to healthy controls (OR 0.345, 95% Cl 0.186-0.639, p = 0.001). Besides this, allele frequencies of IL-18 (-137 G/C) and IL-18 (-607 C/A) gene variations in patient with bladder cancer and healthy control groups were significantly different from the Hardy-Weinberg distribution (p < 0.05). For IL-18 (-137 G/C) and IL-18 (-607 C/A) gene variations, significant difference was determined between the bladder cancer patient and healthy control groups in terms of GC-CA (OR 0.381, 95% Cl 0.203-0.714, p = 0.002), GC-CC (OR 2.147, 95% Cl 1.013-4.550, p = 0.043), GG-AA (OR 0.431, 95% Cl 0.365-0.509, p = 0.049), and GG-CC (OR 2.476, 95% Cl 1.177-5.208, p = 0.015) haplotypes.

CONCLUSION

In our study, CC genotype of IL-18 (-607 C/A) gene variation was determined as genetic risk factor for bladder cancer development. In bladder cancer patient and healthy control groups, G and C allele frequencies of IL-18 (-137 G/C) gene variation, and C and A allele frequencies of IL-18 (-607 C/A) gene variation were determined significantly different from the Hardy-Weinberg distribution.

摘要

背景

本研究旨在探讨白细胞介素-18(IL-18)基因变异在土耳其色雷斯人群膀胱癌发生中的作用。

方法

本研究共纳入 103 例膀胱癌患者和 81 例健康对照者。采用聚合酶链反应(PCR)方法检测 IL-18(-137 G/C)和 IL-18(-607 C/A)基因变异的基因型分布。

结果

与健康对照组相比,膀胱癌患者中 IL-18(-607 C/A)基因变异的 CC 纯合基因型显著升高(OR 0.345,95%CI 0.186-0.639,p=0.001)。此外,膀胱癌患者和健康对照组中 IL-18(-137 G/C)和 IL-18(-607 C/A)基因变异的等位基因频率与 Hardy-Weinberg 分布显著不同(p<0.05)。对于 IL-18(-137 G/C)和 IL-18(-607 C/A)基因变异,膀胱癌患者和健康对照组在 GC-CA(OR 0.381,95%CI 0.203-0.714,p=0.002)、GC-CC(OR 2.147,95%CI 1.013-4.550,p=0.043)、GG-AA(OR 0.431,95%CI 0.365-0.509,p=0.049)和 GG-CC(OR 2.476,95%CI 1.177-5.208,p=0.015)单倍型方面存在显著差异。

结论

在本研究中,IL-18(-607 C/A)基因变异的 CC 基因型被确定为膀胱癌发生的遗传危险因素。在膀胱癌患者和健康对照组中,IL-18(-137 G/C)基因变异的 G 和 C 等位基因频率以及 IL-18(-607 C/A)基因变异的 C 和 A 等位基因频率与 Hardy-Weinberg 分布存在显著差异。

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