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非酒精性脂肪性肝炎向肝细胞癌的自然进展

Natural Progression of Non-Alcoholic Steatohepatitis to Hepatocellular Carcinoma.

作者信息

Ramai Daryl, Tai Waqqas, Rivera Michelle, Facciorusso Antonio, Tartaglia Nicola, Pacilli Mario, Ambrosi Antonio, Cotsoglou Christian, Sacco Rodolfo

机构信息

Department of Internal Medicine, The Brooklyn Hospital Center, Brooklyn, NY 11201, USA.

Section of Gastroenterology, Department of Medical and Surgical Sciences, University of Foggia, 71122 Foggia, Italy.

出版信息

Biomedicines. 2021 Feb 12;9(2):184. doi: 10.3390/biomedicines9020184.

Abstract

Non-alcoholic steatohepatitis (NASH) is a chronic and progressive form of non-alcoholic fatty liver disease (NAFLD). Its global incidence is increasing which makes NASH an epidemic and a public health threat. Due to repeated insults to the liver, patients are at risk for developing hepatocellular carcinoma (HCC). The progression of NASH to HCC was initially defined according to a two-hit model which involved the development of steatosis, followed by lipid peroxidation and inflammation. However, current research defines a "multi-hit" or "multi-parallel hit" model which synthesizes several contributing pathways involved in progressive fibrosis and oncogenesis. This perspective considers the effects of cellular, genetic, immunologic, metabolic, and endocrine pathways leading up to HCC which underscores the complexity of this condition. This article will provide an updated review of the pathogenic mechanisms leading from NASH to HCC as well as an exploration of the role of biomarkers and screening.

摘要

非酒精性脂肪性肝炎(NASH)是一种慢性、进行性的非酒精性脂肪性肝病(NAFLD)。其全球发病率正在上升,这使得NASH成为一种流行病,并对公共卫生构成威胁。由于肝脏反复受到损伤,患者有发展为肝细胞癌(HCC)的风险。NASH向HCC的进展最初是根据“二次打击”模型定义的,该模型包括脂肪变性的发展,随后是脂质过氧化和炎症。然而,目前的研究定义了一种“多重打击”或“多平行打击”模型,该模型综合了参与进行性纤维化和肿瘤发生的几种促成途径。这一观点考虑了导致HCC的细胞、遗传、免疫、代谢和内分泌途径的影响,突出了这种疾病的复杂性。本文将对从NASH到HCC的致病机制进行更新综述,并探讨生物标志物和筛查的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/865c/7918599/1a2434f59e1a/biomedicines-09-00184-g001.jpg

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