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Furthermore, the effects of selective CK1δ inhibition during zebrafish embryonic development were analyzed in vivo. To this end, the kinetic parameters of human CK1 isoforms were compared with those of zebrafish orthologues. Methods: In this study, we investigated the suitability of the zebrafish model system for the evaluation of such CK1 inhibitors.

There is increasing evidence that CK1 isoform specific small molecule inhibitors, including CK1δ- and CK1ε-specific inhibitors of Wnt production (IWP)-based small molecules with structural similarity to benzimidazole compounds, have promising therapeutic potential. Mutations or dysregulation of kinases in general and of CK1 in particular are known to promote the development of cancer, neurodegenerative diseases and inflammation. Introduction: The CK1 family is involved in a variety of physiological processes by regulating different signaling pathways, including the Wnt/β-catenin, the Hedgehog and the p53 signaling pathways.

3Institute of Pharmacy, Christian-Albrechts-University of Kiel, Kiel, Germany.

2Molecular Cardiology, Department of Internal Medicine II, University Hospital Ulm, Ulm, Germany.

1Surgery Center, Department of General- and Visceral Surgery, University Hospital Ulm, Ulm, Germany.

GraphPad Prism.Laura Meier 1 † ‡ Bernd Martin Gahr 2 ‡ Aileen Roth 1 Adrian Gihring 1 Stefan Kirschner 3 Clemens Woitaske-Proske 3 Joana Baier 3 Christian Peifer 3 Steffen Just 2 Uwe Knippschild 1*

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