Back to Search
Start Over
A Putative Frizzled 7-Targeting Compound Acts as a Firefly Luciferase Inhibitor.
- 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.
- Subjects :
- Humans
HEK293 Cells
Structure-Activity Relationship
Molecular Docking Simulation
Animals
Frizzled Receptors metabolism
Frizzled Receptors antagonists & inhibitors
Luciferases, Firefly metabolism
Luciferases, Firefly antagonists & inhibitors
Luciferases, Firefly genetics
Wnt Signaling Pathway drug effects
Subjects
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