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Humanized liver mouse models in preclinical drug development: current status, translation challenges and emerging
Xumiao Zhang1, Lu Lu1, Wei Xiao2
1Department of Hematologic Oncology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, China.
None:
Humanized liver mouse models are constructed by engrafting primary human hepatocytes into immunodeficient mouse livers, thereby reconstructing human-specific metabolic and transport pathways and significantly improving the prediction of pharmacokinetics, drug interactions and hepatotoxicity. These models have been widely applied to MASLD/MASH, fibrosis, hepatocellular carcinoma and viral hepatitis research but remain constrained by the absence of intestinal CYP3A4 expression and functional immune compartments. Emerging approaches, including dual humanization, non-parenchymal cell supplementation, vascularized 3D bioprinting and application of patient-derived hepatocytes, combined with advanced in vitro and computational platforms, further strengthen translational fidelity, reduce R&D attrition and expand the scope for modeling complex metabolism-related diseases.
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