Use of Zebrafish in Drug Discovery Toxicology
- Cassar, S., Adatto, I., Freeman, J.L., Gamse, J.T., Iturria, I., Lawrence, C., Muriana, A., Peterson, R., Van Cruchten, S., Zon, L.
- Chemical Research in Toxicology 33(1): 95-118 (Review)
- Registered Authors
- Adatto, Isaac, Freeman, Jennifer, Gamse, Josh, Lawrence, Christian, Muriana, Arantza, Peterson, Randall, Van Cruchten, Steven, Zon, Leonard I.
- MeSH Terms
- Animal Use Alternatives
- Drug Discovery*
- Drug-Related Side Effects and Adverse Reactions
- Embryo, Nonmammalian
- Models, Animal*
- Toxicity Tests/methods*
- 31625720 Full text @ Chem. Res. Toxicol.
Cassar, S., Adatto, I., Freeman, J.L., Gamse, J.T., Iturria, I., Lawrence, C., Muriana, A., Peterson, R., Van Cruchten, S., Zon, L. (2019) Use of Zebrafish in Drug Discovery Toxicology. Chemical Research in Toxicology. 33(1):95-118.
Unpredicted human safety events in clinical trials for new drugs are costly in terms of human health and money. The drug discovery industry attempts to minimize those events with diligent preclinical safety testing. Current standard practices are good at preventing toxic compounds from being tested in the clinic; however, false negative preclinical toxicity results are still a reality. Continual improvement must be pursued in the preclinical realm. Higher quality therapies can be brought forward with more information about potential toxicities and associated mechanisms. The zebrafish model is a bridge between in vitro assays and mammalian in vivo studies. This model is powerful in its breadth of application and tractability for research. In the past two decades our understanding of disease biology and drug toxicity has grown significantly owing to thousands of studies on this tiny vertebrate. This review summarizes challenges and strengths of the model, discusses the 3Rs value that it can deliver, highlights translatable and untranslatable biology, and brings together reports from recent studies with zebrafish focusing on new drug discovery toxicology.
Genes / Markers
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Engineered Foreign Genes