医学
肝硬化
疾病
肝病
离体
临床前试验
生物信息学
脂肪肝
脂肪变性
临床试验
药品
治疗方法
病理
精密医学
药理学
慢性肝病
重症监护医学
动物模型
系统药理学
体内
药物开发
代谢性疾病
代谢活性
计算生物学
梅德林
作者
Alissa M. Cutrone,Heidi Yeh,Korkut Uygun,O. Berk Usta
标识
DOI:10.1146/annurev-bioeng-081325-053420
摘要
Metabolic dysfunction-associated steatotic liver disease (MASLD) is the most prevalent hepatic pathology worldwide, with significant potential for progression to cirrhosis and ultimately end-stage liver disease. Accordingly, a wide range of preclinical models have been developed to better understand the disease mechanisms and progression as well as to accelerate drug discovery. These include in vitro, ex vivo, and in vivo models, which offer unique advantages yet differ in terms of disease driver, species used, and biological complexity-ranging from benchtop cellular systems to whole organs and organisms. In this review, we provide a comprehensive overview of the technologies currently used for the study of MASLD, with a focus on how standardization of disease progression across models may aid therapeutic development.
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