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Tie2/血管生成素系统在丙型肝炎病毒诱导的肝细胞癌中的潜在作用

Potential Role of the Tie2/ Angiopoietin System in Hepatitis C Virus- Induced Hepatocellular Carcinoma.

作者信息

Fouad Rabab, Madkour Bothaina, Zahran Manal, Abdel Rahim Ali, Salem Dalia, Nassar Omar, Elnashar Shereen, Mahmoud Ola

机构信息

Department of Hematology, Theodor Bilharz Research Institute (TBRI), Giza, Egypt.

Department of Hepato-Gastroenterology, Theodor Bilharz Research Institute (TBRI), Giza, Egypt.

出版信息

Asian Pac J Cancer Prev. 2024 Dec 1;25(12):4137-4144. doi: 10.31557/APJCP.2024.25.12.4137.

Abstract

BACKGROUND

The Tie2/Ang pathway was found to be involved in forming tumor blood vessels in various tumors. The goal of this study was to evaluate the value of Tie2/Ang pathway as a novel biomarkers for the early detection of chronic hepatitis C virus (CHC)-related hepatocellular carcinoma (HCC). And the possibility of their future application in HCC treatment.

METHODS

Flow cytometry was performed to identify and count Tie2 expressing monocytes (TEMs) in peripheral blood monocytes from HCC patients (n = 25), CHC cirrhotic patients (n = 25) and healthy volunteers (n = 25). In addition, Angiopoietin 1 and 2 (Ang) levels in the serum were determined by enzyme linked immunosorbent assay (ELIZA).

RESULTS

Percentage of TEMs in peripheral blood monocytes, serum Ang2 levels and Ang2/Ang1 ratio significantly increased in HCC patients compared with CHC patients and healthy controls (P< 0.001). However significant increase was only noticed in serum Ang1 levels in HCC group compared to the control group (P <0.05).

CONCLUSIONS

TEMs may promote angiogenesis in HCC regarding the Ang2/Tie2 signal pathway. Percentage of TEMs in peripheral blood monocytes, Ang2 serum levels and Ang2/Ang1 ratio may be applied as a biomarkers for identifying CHC-related HCC. Moreover, inhibiting the proangiogenic functions of this pathway may represent a promising strategy to improve the efficacy of current treatments for HCC.

摘要

背景

发现Tie2/Ang通路参与多种肿瘤的血管形成。本研究的目的是评估Tie2/Ang通路作为慢性丙型肝炎病毒(CHC)相关肝细胞癌(HCC)早期检测的新型生物标志物的价值,以及它们未来在HCC治疗中应用的可能性。

方法

采用流式细胞术鉴定并计数HCC患者(n = 25)、CHC肝硬化患者(n = 25)和健康志愿者(n = 25)外周血单核细胞中表达Tie2的单核细胞(TEMs)。此外,采用酶联免疫吸附测定(ELISA)法测定血清中血管生成素1和2(Ang)的水平。

结果

与CHC患者和健康对照组相比,HCC患者外周血单核细胞中TEMs的百分比、血清Ang2水平和Ang2/Ang1比值显著升高(P < 0.001)。然而,与对照组相比,仅在HCC组中观察到血清Ang1水平显著升高(P < 0.05)。

结论

关于Ang2/Tie2信号通路,TEMs可能促进HCC中的血管生成。外周血单核细胞中TEMs的百分比、血清Ang2水平和Ang2/Ang1比值可作为识别CHC相关HCC的生物标志物。此外,抑制该通路的促血管生成功能可能是提高当前HCC治疗疗效的一种有前景的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9703/12008347/5b7955f5ac3a/APJCP-25-4137-g001.jpg

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