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白细胞介素 4、白细胞介素 17 和 CD163 免疫表达与慢性丙型肝炎患者及其相关肝细胞癌的白细胞介素 6 基因多态性。

IL-4, IL-17 and CD163 Immunoexpression and IL-6 Gene Polymorphism in Chronic Hepatitis C Patients and Associated Hepatocellular Carcinoma.

机构信息

Department oF Pathology, Theodor Bilharz Research Institute, Giza, Egypt.

Faculty of Biotechnology, October University for Modern Sciences and Arts, Giza, Egypt.

出版信息

Asian Pac J Cancer Prev. 2021 Apr 1;22(4):1105-1113. doi: 10.31557/APJCP.2021.22.4.1105.

DOI:10.31557/APJCP.2021.22.4.1105
PMID:33906302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8325124/
Abstract

OBJECTIVE

To assess the expression of IL-4, IL-17 and CD-163 as well as study of IL6-572 C/G gene polymorphism in chronic HCV and HCC on top of HCV.

METHODS

Sixty HCC specimens and 60 adjacent hepatic tissue with HCV of different grades of necro-inflammation and different stages of fibrosis. In addition to 55 HCV, 60 HCC and 50 healthy venous blood samples for evaluation of IL6-572 C/G gene polymorphism.

RESULTS

high expression of IL-4, IL-17 and CD163 in higher grades of activity, late stages of fibrosis and higher degrees of steatosis of HCV. IL-4 and CD163 showed higher expression in advanced grades of HCC, while IL-17 more expressed in lower grades. No significant difference in IL6-572 C/G gene polymorphism among studied groups regarding G/C, G/G, C/C frequencies or G and C allele's frequencies.

CONCLUSION

IL-4, IL-17 and CD163 were associated with HCV severity. Their expression in HCC suggests their important role in HCC development. Blocking of these proteins may be a good target to control inflammation in HCV and can hinder progression to cirrhosis then to HCC. On the other hand, IL6-572 promoter gene polymorphism is neither associated with HCV infection nor with HCC development and its progression.
.

摘要

目的

评估慢性 HCV 和 HCC 中 IL-4、IL-17 和 CD-163 的表达,并研究 IL6-572 C/G 基因多态性。

方法

对 60 例 HCC 标本和 60 例伴有不同坏死炎症程度和不同纤维化阶段的 HCV 的肝组织进行研究。除了 55 例 HCV 外,还评估了 60 例 HCC 和 50 例健康静脉血样本的 IL6-572 C/G 基因多态性。

结果

IL-4、IL-17 和 CD163 在 HCV 活性较高、纤维化晚期和脂肪变性程度较高的患者中高表达。IL-4 和 CD163 在 HCC 的晚期分级中表达较高,而 IL-17 在较低的分级中表达较高。在研究组中,IL6-572 C/G 基因多态性在 G/C、G/G、C/C 频率或 G 和 C 等位基因频率方面没有显著差异。

结论

IL-4、IL-17 和 CD163 与 HCV 的严重程度有关。它们在 HCC 中的表达表明它们在 HCC 发展中起着重要作用。阻断这些蛋白可能是控制 HCV 炎症的一个很好的靶点,并可以阻止其进展为肝硬化,然后进展为 HCC。另一方面,IL6-572 启动子基因多态性既与 HCV 感染无关,也与 HCC 的发展及其进展无关。

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