Target intelligence / Profile preview

Yes-associated protein 1 (YAP1) - Transcriptional enhancer factor domain (TEAD) protein-protein interaction (YAP-TEAD PPI)

Target
YAP-TEAD PPI
Molecular classification
Transcription factor, Protein-protein interaction, Other
01

Overview

The Yes-associated protein 1 (YAP1) - Transcriptional enhancer factor domain (TEAD) protein-protein interaction is the central terminal component of the Hippo signaling pathway, which plays a fundamental role in controlling organ size, cell proliferation, and tissue homeostasis (Nature Reviews Drug Discovery, 2019). YAP1 and its paralog TAZ function as transcriptional co-activators that lack intrinsic DNA-binding activity and must interact with TEAD family transcription factors (TEAD1-4) to regulate the expression of genes that promote cell survival and epithelial-to-mesenchymal transition (UniProt, P46937). In many human cancers, particularly those harboring mutations in Neurofibromin 2 (NF2) or Large Tumor Suppressor Kinases (LATS1/2), the Hippo pathway is inactivated, leading to the constitutive nuclear localization of YAP1 and hyperactivation of TEAD-mediated transcription (PubMed, 30447548). Therapeutic strategies targeting this interaction include small molecules that bind to the highly conserved palmitoylation pocket of TEAD or directly block the YAP-TEAD binding interface (Journal of Medicinal Chemistry, 2022). Several inhibitors, such as VT3989 and IK-930, are currently in clinical development for the treatment of malignant pleural mesothelioma and other Hippo-pathway-deficient solid tumors (ClinicalTrials.gov, NCT04665206).

Other names
YAP1-TEAD interactionTAZ-TEAD interactionHippo pathway effector complexYAP-TEAD complex
02

Mechanism of action

Inhibition of the protein-protein interaction between the transcriptional co-activators YAP1 or TAZ and the TEAD family of transcription factors, primarily through small-molecule binding to the TEAD palmitoylation pocket or the YAP-binding interface, which prevents the formation of a functional transcriptional complex (Nature Reviews Drug Discovery, 2019; Journal of Medicinal Chemistry, 2022).

03

Biological functions

Signal transductionCell cycleCell proliferationOrgan size controlTissue regenerationOther
04

Disease associations

CancerOther
05

Safety considerations

Impairment of normal tissue regenerationPotential liver toxicityPotential renal toxicityGastrointestinal adverse effects
06

Interacting drugs

VT3989

4 more in the full profile.

07

Biomarkers

NF2 mutationLATS1/2 mutationYAP1 nuclear localizationCTGF expressionCYR61 expression

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