Toulotte Florine, Coevoet Mathilde, Liberelle Maxime, Bailly Fabrice, Zagiel Benjamin, Gelin Muriel, Allemand Frédéric, Fourquet Patrick, Melnyk Patricia, Guichou Jean-François, Cotelle Philippe
Univ Lille, INSERM, CHU Lille, UMR-S 1172, Lille Neuroscience and Cognition Research Center, F-59000, Lille, France.
Centre de Biologie Structurale (CBS), CNRS, INSERM, Univ Montpellier, F-34090, Montpellier, France.
Eur J Med Chem. 2025 Jan 15;282:117026. doi: 10.1016/j.ejmech.2024.117026. Epub 2024 Nov 12.
The Hippo pathway controls in organ size and tissue homeostasis through regulating cell growth, proliferation and apoptosis. Phosphorylation of the transcription co-activator YAP (Yes associated protein) and TAZ (Transcriptional coactivator with PDZ-binding motif) regulates their nuclear import and therefore their interaction with TEAD (Transcriptional Enhanced Associated Domain). YAP, TAZ and TEADs are dysregulated in several solid cancers making YAP/TAZ-TEAD interaction a new anti-cancer target. We identified by screening a small in-house library, 5-benzyloxindole which binds to hTEAD2 at its internal/palmitate pocket. Its optimization led to covalent inhibitors bearing different warhead. Soaking with hTEAD2 gave seven new crystal structures where the ligands occupied palmitate pocket. 5-Benzyloxyindoles armed with vinylsulfamide moiety inhibit YAP/TAZ-TEAD target genes expression and breast cancer cell proliferation at micromolar concentration.