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A Putative Frizzled 7-Targeting Compound Acts as a Firefly Luciferase Inhibitor.

Authors :
Kinsolving J
Grätz L
Voss JH
Löw B
Shorter E
Jude B
Lanner JT
Löber S
Gmeiner P
Schulte G
Source :
Journal of medicinal chemistry [J Med Chem] 2024 Dec 26; Vol. 67 (24), pp. 22332-22341. Date of Electronic Publication: 2024 Dec 13.
Publication Year :
2024

Abstract

The Frizzled family (FZD <subscript>1-10</subscript> ) of G protein-coupled receptors regulates WNT signaling mediating proliferative input. Dysregulation of FZD <subscript>7</subscript> and exaggerated WNT/β-catenin signaling is frequently observed in intestinal cancers. Therefore, it is attractive to develop therapeutics targeting FZD <subscript>7</subscript> for cancer treatment. Structure-based virtual screening has identified compound 28, which inhibited WNT/β-catenin signaling based on the luciferase-based reporter gene TOPFlash assay. However, upon pharmacological validation, compound 28 rather acts as a potent Firefly luciferase (Fluc) inhibitor (IC <subscript>50</subscript> = 30 nM), matching the reported IC <subscript>50</subscript> for compound 28-mediated inhibition in the TOPFlash assay. Moreover, we employed Fluc-independent assays, a FZD <subscript>7</subscript> -focused bioluminescence resonance energy transfer biosensor and quantitative PCR, to emphasize the inability of compound 28 to inhibit the WNT-3A-induced conformational dynamics in FZD <subscript>7</subscript> and transcription of Axin2, a WNT target gene. Thus, we underline the importance of counter screens to validate compounds that interfere with the detection technology used for compound screening.

Details

Language :
English
ISSN :
1520-4804
Volume :
67
Issue :
24
Database :
MEDLINE
Journal :
Journal of medicinal chemistry
Publication Type :
Academic Journal
Accession number :
39670643
Full Text :
https://doi.org/10.1021/acs.jmedchem.4c02766