Literature DB >> 24496635

Fishing for teratogens: a consortium effort for a harmonized zebrafish developmental toxicology assay.

Jonathan S Ball1, Donald B Stedman, Jedd M Hillegass, Cindy X Zhang, Julie Panzica-Kelly, Aleasha Coburn, Brian P Enright, Belen Tornesi, Hamid R Amouzadeh, Malcolm Hetheridge, Anne-Lee Gustafson, Karen A Augustine-Rauch.   

Abstract

A consortium of biopharmaceutical companies previously developed an optimized Zebrafish developmental toxicity assay (ZEDTA) where chorionated embryos were exposed to non-proprietary test compounds from 5 to 6 h post fertilization and assessed for morphological integrity at 5 days post fertilization. With the original 20 test compounds, this achieved an overall predictive value for teratogenicity of 88% of mammalian in vivo outcome [Gustafson, A. L., Stedman, D. B., Ball, J., Hillegass, J. M., Flood, A., Zhang, C. X., Panzica-Kelly, J., Cao, J., Coburn, A., Enright, B. P., et al. (2012). Interlaboratory assessment of a harmonized Zebrafish developmental toxicology assay-Progress report on phase I. Reprod. Toxicol. 33, 155-164]. In the second phase of this project, 38 proprietary pharmaceutical compounds from four consortium members were evaluated in two laboratories using the optimized method using either pond-derived or cultivated-strain wild-type Zebrafish embryos at concentrations up to 100μM. Embryo uptake of all compounds was assessed using liquid chromatography-tandem mass spectrometry. Twenty eight of 38 compounds had a confirmed embryo uptake of >5%, and with these compounds the ZEDTA achieved an overall predictive value of 82% and 65% at the two respective laboratories. When low-uptake compounds (≤ 5%) were retested with logarithmic concentrations up to 1000μM, the overall predictivity across all 38 compounds was 79% and 62% respectively, with the first laboratory achieving 74% sensitivity (teratogen detection) and 82% specificity (non-teratogen detection) and the second laboratory achieving 63% sensitivity (teratogen detection) and 62% specificity (non-teratogen detection). Subsequent data analyses showed that technical differences rather than strain differences were the primary contributor to interlaboratory differences in predictivity. Based on these results, the ZEDTA harmonized methodology is currently being used for compound assessment at lead optimization stage of development by 4/5 of the consortium companies.

Entities:  

Keywords:  Zebrafish; developmental toxicity assay; embryo; interlaboratory assessment; pharmaceutical compounds; teratogenicity; teratogenicity screen

Mesh:

Substances:

Year:  2014        PMID: 24496635     DOI: 10.1093/toxsci/kfu017

Source DB:  PubMed          Journal:  Toxicol Sci        ISSN: 1096-0929            Impact factor:   4.849


  19 in total

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Review 2.  Zebrafish in Toxicology and Environmental Health.

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Review 3.  Nrf2 and Nrf2-related proteins in development and developmental toxicity: Insights from studies in zebrafish (Danio rerio).

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6.  Pluripotent stem cell assays: Modalities and applications for predictive developmental toxicity.

Authors:  Aldert H Piersma; Nancy C Baker; George P Daston; Burkhard Flick; Michio Fujiwara; Thomas B Knudsen; Horst Spielmann; Noriyuki Suzuki; Katya Tsaioun; Hajime Kojima
Journal:  Curr Res Toxicol       Date:  2022-05-13

Review 7.  Use of Zebrafish in Drug Discovery Toxicology.

Authors:  Steven Cassar; Isaac Adatto; Jennifer L Freeman; Joshua T Gamse; Iñaki Iturria; Christian Lawrence; Arantza Muriana; Randall T Peterson; Steven Van Cruchten; Leonard I Zon
Journal:  Chem Res Toxicol       Date:  2019-11-16       Impact factor: 3.739

8.  The nematode Caenorhabditis elegans as a tool to predict chemical activity on mammalian development and identify mechanisms influencing toxicological outcome.

Authors:  Philippa H Harlow; Simon J Perry; Stephanie Widdison; Shannon Daniels; Eddie Bondo; Clemens Lamberth; Richard A Currie; Anthony J Flemming
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9.  A targeted gene expression platform allows for rapid analysis of chemical-induced antioxidant mRNA expression in zebrafish larvae.

Authors:  Margaret G Mills; Evan P Gallagher
Journal:  PLoS One       Date:  2017-02-17       Impact factor: 3.240

Review 10.  Retinoids and developmental neurotoxicity: Utilizing toxicogenomics to enhance adverse outcome pathways and testing strategies.

Authors:  Hao Chen; Megan A Chidboy; Joshua F Robinson
Journal:  Reprod Toxicol       Date:  2020-06-13       Impact factor: 3.143

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