Centenary Institute, The University of Sydney, Newtown, New South Wales, 2042, Australia; The University of Sydney Faculty of Medicine and Health, New South Wales, 2006, Australia.
Centenary Institute, The University of Sydney, Newtown, New South Wales, 2042, Australia; The University of Sydney Faculty of Medicine and Health, New South Wales, 2006, Australia.
Biochim Biophys Acta Mol Basis Dis. 2019 May 1;1865(5):993-1002. doi: 10.1016/j.bbadis.2018.08.009. Epub 2018 Aug 10.
Hepatocellular carcinoma (HCC) represents ~90% of all cases of primary liver cancer and occurs predominantly in patients with underlying chronic liver disease and cirrhosis. Establishing appropriate animal models for HCC is required for basic and translational studies, especially the models that can recapitulate one of the human disease settings. Current animal models can be categorized as chemically-induced, genetically-engineered, xenograft, or a combination of these with each other or with a metabolic insult. A single approach to resemble human HCC in animals is not sufficient. Combining pathogenic insults in animal models may more realistically recapitulate the multiple etiologic agents occurring in humans. Combining chemical injury with metabolic disorder or alcohol consumption in mice reduces the time taken to hepatocarcinogenesis. Genetically-engineering weak activation of HCC-promoting pathways combined with disease-specific injury models will possibly mimic the pathophysiology of human HCC in distinct clinical settings.
肝细胞癌(HCC)占原发性肝癌的 90%左右,主要发生在有潜在慢性肝病和肝硬化的患者中。建立适当的 HCC 动物模型对于基础和转化研究是必要的,特别是能够重现人类疾病状态之一的模型。目前的动物模型可分为化学诱导、基因工程、异种移植,或彼此之间以及与代谢损伤相结合的模型。单一的方法不足以在动物中模拟人类 HCC。在动物模型中结合致病因素的刺激可能更真实地再现人类中发生的多种病因。在小鼠中结合化学损伤与代谢紊乱或酒精摄入可减少肝致癌发生的时间。结合 HCC 促进途径的弱激活的基因工程与特定疾病的损伤模型,可能会在不同的临床环境中模拟人类 HCC 的病理生理学。