非酒精性脂肪性肝炎导致肝细胞癌的临床前模型

Q1 Biochemistry, Genetics and Molecular Biology Advances in biological regulation Pub Date : 2023-01-01 DOI:10.1016/j.jbior.2022.100925
Christopher D. Green, Sarah Spiegel
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引用次数: 0

摘要

肝细胞癌(HCC)是全球癌症相关死亡的第三大原因,其发病率因地方性肥胖和非酒精性脂肪性肝炎(NASH)相关癌症负担的增加而增加。尽管人们对NASH驱动的人类HCC的临床和组织病理学知之甚少,但其病因尚不清楚,缺乏可靠的生物标志物和有限的有效治疗方法。由于缺乏标准化的动物模型来概括在人类中观察到的NASH向HCC的逐渐进展,这一进展受到了阻碍。在这里,我们回顾了现有的小鼠模型及其对研究NASH驱动的HCC的适用性,特别强调了我们最近开发的一种临床前模型,该模型忠实地模拟了人类疾病进展的所有临床终点。此外,它是高度可翻译的,允许使用基因靶向小鼠,并且适合于获得NASH如何发展为HCC的知识和开发新的治疗靶点。
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Preclinical models of non-alcoholic steatohepatitis leading to hepatocellular carcinoma

Hepatocellular carcinoma (HCC) is the third leading cause of cancer related deaths worldwide and its incidence is increasing due to endemic obesity and the growing burden of non-alcoholic steatohepatitis (NASH) associated liver cancer. Although much is known about the clinical and histological pathology of NASH-driven HCC in humans, its etiology remains unclear and there is a lack of reliable biomarkers and limited effective therapies. Progress has been hampered by the scarcity of standardized animal models that recapitulate the gradual progression of NASH towards HCC observed in humans. Here we review existing mouse models and their suitability for studying NASH-driven HCC with special emphasis on a preclinical model that we recently developed that faithfully mimics all the clinical endpoints of progression of the human disease. Moreover, it is highly translatable, allows the use of gene-targeted mice, and is suitable for gaining knowledge of how NASH progresses to HCC and development of new targets for treatment.

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来源期刊
Advances in biological regulation
Advances in biological regulation Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
8.90
自引率
0.00%
发文量
41
审稿时长
17 days
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