Abstract
Preclinical evaluation of drug candidates in experimental animal models is an essential step in drug development. Humanized mouse models have emerged as a promising alternative to traditional animal models. The purpose of this mini-review is to provide a brief survey of currently available mouse models for studying human xenobiotic metabolism. Here, we describe both genetic humanization and human liver chimeric mouse models, focusing on the advantages and limitations while outlining their key features and applications. Although this field of biomedical science is relatively young, these humanized mouse models have the potential to transform preclinical drug testing and eventually lead to a more cost-effective and rapid development of new therapies.
Footnotes
- Received June 25, 2018.
- Accepted August 3, 2018.
Q.-Y.Z. and X.D. are supported in part by the National Institutes of Health (NIH) [Grants CA092596, ES020867, and GM082978]. K.-D.B. is supported by the NIH [Grants HL134510 and DK115461] and the Texas Hepatocellular Carcinoma Consortium (THCCC) (CPRIT #RP150587). K.-D.B., M.B., F.P.P. have a financial interest in Avachrome Inc. No other potential conflicts of interest relevant to this article are reported.
- Copyright © 2018 by The American Society for Pharmacology and Experimental Therapeutics
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