Article
作者: Gelin, Muriel ; Bailly, Fabrice ; MELNYK, Patricia ; COEVOET, Mathilde ; ALLEMAND, Frédéric ; Jean-François, G.U.I.C.H.O.U. ; GELIN, Muriel ; TOULOTTE, Florine ; Liberelle, Maxime ; Melnyk, Patricia ; Cotelle, Philippe ; Guichou, Jean-François ; COTELLE, Philippe ; Zagiel, Benjamin ; FOURQUET, Patrick ; LIBERELLE, Maxime ; Toulotte, Florine ; BAILLY, Fabrice ; Allemand, Frédéric ; ZAGIEL, Benjamin ; Coevoet, Mathilde ; Fourquet, Patrick
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.