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乙型肝炎病毒相关肝细胞癌在发病机制及临床意义方面的独特特征

Unique Features of Hepatitis B Virus-Related Hepatocellular Carcinoma in Pathogenesis and Clinical Significance.

作者信息

Wang Sheng-Han, Yeh Shiou-Hwei, Chen Pei-Jer

机构信息

Hepatitis Research Center, National Taiwan University Hospital, Taipei 10002, Taiwan.

Graduate Institute of Microbiology, National Taiwan University College of Medicine, Taipei 10051, Taiwan.

出版信息

Cancers (Basel). 2021 May 18;13(10):2454. doi: 10.3390/cancers13102454.

Abstract

Hepatitis B virus (HBV) infection is one of the important risk factors for hepatocellular carcinoma (HCC) worldwide, accounting for around 50% of cases. Chronic hepatitis B infection generates an inflammatory microenvironment, in which hepatocytes undergoing repeated cycles of damage and regeneration accumulate genetic mutations predisposing them to cancer. A striking male dominance in HBV-related HCC highlights the influence of sex hormones which interact with viral factors to influence carcinogenesis. HBV is also considered an oncogenic virus since its X and surface mutant proteins showed tumorigenic activity in mouse models. The other unique mechanism is the insertional mutagenesis by integration of HBV genome into hepatocyte chromosomes to activate oncogenes. HCC survival largely depends on tumor stages at diagnosis and effective treatment. However, early diagnosis by the conventional protein biomarkers achieves limited success. A new biomarker, the circulating virus-host chimera DNA from HBV integration sites in HCC, provides a liquid biopsy approach for monitoring the tumor load in the majority of HBV-HCC patients. To maximize the efficacy of new immunotherapies or molecular target therapies, it requires better classification of HCC based on the tumor microenvironment and specific carcinogenic pathways. An in-depth study may benefit both the diagnosis and treatment of HBV-related HCC.

摘要

乙型肝炎病毒(HBV)感染是全球肝细胞癌(HCC)的重要危险因素之一,约占病例的50%。慢性乙型肝炎感染会产生炎症微环境,在这种环境中,经历反复损伤和再生循环的肝细胞会积累基因突变,使其易患癌症。HBV相关肝癌中男性明显占主导地位,这突出了性激素的影响,性激素与病毒因素相互作用影响致癌作用。HBV也被认为是一种致癌病毒,因为其X蛋白和表面突变蛋白在小鼠模型中显示出致瘤活性。另一个独特的机制是HBV基因组整合到肝细胞染色体中激活癌基因的插入诱变。HCC的生存率很大程度上取决于诊断时的肿瘤分期和有效治疗。然而,通过传统蛋白质生物标志物进行早期诊断取得的成功有限。一种新的生物标志物,即HCC中HBV整合位点的循环病毒-宿主嵌合DNA,为监测大多数HBV-HCC患者的肿瘤负荷提供了一种液体活检方法。为了使新的免疫疗法或分子靶向疗法的疗效最大化,需要根据肿瘤微环境和特定致癌途径对HCC进行更好的分类。深入研究可能对HBV相关HCC的诊断和治疗都有益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9f5/8158142/4d7aecea80cc/cancers-13-02454-g001.jpg

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