类有机物
药品
医学
药物毒性
肝细胞癌
原发性硬化性胆管炎
药物开发
胆道
病理
生物
癌症研究
疾病
药理学
内科学
遗传学
作者
Haoyu Fang,Haoying Xu,Jiong Yu,Hongcui Cao,Lanjuan Li
出处
期刊:Biomolecules
[Multidisciplinary Digital Publishing Institute]
日期:2024-07-04
卷期号:14 (7): 794-794
被引量:14
摘要
Many drug and therapeutic modalities have emerged over the past few years. However, successful commercialization is dependent on their safety and efficacy evaluations. Several preclinical models are available for drug-screening and safety evaluations, including cellular- and molecular-level models, tissue and organoid models, and animal models. Organoids are three-dimensional cell cultures derived from primary tissues or stem cells that are structurally and functionally similar to the original organs and can self-renew, and they are used to establish various disease models. Human hepatobiliary organoids have been used to study the pathogenesis of diseases, such as hepatitis, liver fibrosis, hepatocellular carcinoma, primary sclerosing cholangitis and biliary tract cancer, as they retain the physiological and histological characteristics of the liver and bile ducts. Here, we review recent research progress in validating drug toxicity, drug screening and personalized therapy for hepatobiliary-related diseases using human hepatobiliary organoid models, discuss the challenges encountered in current research and evaluate the possible solutions.
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