河马信号通路
化学
细胞生物学
细胞生长
PDZ域
HEK 293细胞
激活剂(遗传学)
磷酸化
血浆蛋白结合
基因
生物
转录因子
癌症研究
生物化学
作者
Manon Sturbaut,Fabrice Bailly,Mathilde Coevoet,Pasquale Sileo,Martine Pugnière,Maxime Liberelle,Romain Magnez,Xavier Thuru,Marie‐Christine Chartier‐Harlin,Patricia Melnyk,Muriel Gelin,Frédéric Allemand,Jean‐François Guichou,Philippe Cotelle
标识
DOI:10.1016/j.ejmech.2021.113835
摘要
Abstract The Hippo pathway is involved in organ size control and tissue homeostasis by regulating cell growth, proliferation and apoptosis. It controls the phosphorylation of the transcription co-activator YAP (Yes associated protein) and TAZ (Transcriptional coactivator with PDZ-binding motif) in order to control their nuclear import and their interaction with TEAD (Transcriptional Enhanced Associated Domain). YAP, TAZ and TEADs are dysregulated in several cancers making YAP/TAZ-TEAD interaction a new emerging anti-cancer target. We report the synthesis of a set of trisubstituted pyrazoles which bind to hTEAD2 at the interface 2 revealing for the first time a cryptic pocket created by the movement of the phenol ring of Y382. Compound 6 disrupts YAP/TAZ-TEAD interaction in HEK293T cells and inhibits TEAD target genes and cell proliferation in MDA-MB-231 cells. Compound 6 is therefore the first inhibitor of YAP/TAZ-TEAD targeting interface 2. This molecule could serve with other pan-TEAD inhibitors such as interface 3 ligands, for the delineation of the relative importance of VGLL vs YAP/TAZ in a given cellular model.
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