scholarly journals Recent Therapeutic Approaches to Modulate the Hippo Pathway in Oncology and Regenerative Medicine

Cells ◽  
2021 ◽  
Vol 10 (10) ◽  
pp. 2715
Author(s):  
Evan R. Barry ◽  
Vladimir Simov ◽  
Iris Valtingojer ◽  
Olivier Venier

The Hippo pathway is an evolutionary conserved signaling network that regulates essential processes such as organ size, cell proliferation, migration, stemness and apoptosis. Alterations in this pathway are commonly found in solid tumors and can lead to hyperproliferation, resistance to chemotherapy, compensation for mKRAS and tumor immune evasion. As the terminal effectors of the Hippo pathway, the transcriptional coactivators YAP1/TAZ and the transcription factors TEAD1–4 present exciting opportunities to pharmacologically modulate the Hippo biology in cancer settings, inflammation and regenerative medicine. This review will provide an overview of the progress and current strategies to directly and indirectly target the YAP1/TAZ protein–protein interaction (PPI) with TEAD1–4 across multiple modalities, with focus on recent small molecules able to selectively bind to TEAD, block its autopalmitoylation and inhibit YAP1/TAZ–TEAD-dependent transcription in cancer.

2015 ◽  
Vol 58 (12) ◽  
pp. 4857-4873 ◽  
Author(s):  
Matteo Santucci ◽  
Tatiana Vignudelli ◽  
Stefania Ferrari ◽  
Marco Mor ◽  
Laura Scalvini ◽  
...  

2020 ◽  
Vol 19 (7) ◽  
pp. 480-494 ◽  
Author(s):  
Anwesha Dey ◽  
Xaralabos Varelas ◽  
Kun-Liang Guan

Cancers ◽  
2019 ◽  
Vol 11 (10) ◽  
pp. 1596 ◽  
Author(s):  
Kazem Nouri ◽  
Taha Azad ◽  
Min Ling ◽  
Helena J. Janse van Rensburg ◽  
Alexander Pipchuk ◽  
...  

The Hippo pathway has emerged as a key signaling pathway that regulates a broad range of biological functions, and dysregulation of the Hippo pathway is a feature of a variety of cancers. Given this, some have suggested that disrupting the interaction of the Hippo core component YAP and its paralog TAZ with transcriptional factor TEAD may be an effective strategy for cancer therapy. However, there are currently no clinically available drugs targeting the YAP/TAZ–TEAD interaction for cancer treatment. To facilitate screens for small molecule compounds that disrupt the YAP–TEAD interaction, we have developed the first ultra-bright NanoLuc biosensor to quantify YAP/TAZ–TEAD protein–protein interaction (PPI) both in living cells and also in vitro using biosensor fusion proteins purified from bacteria. Using this biosensor, we have performed an in vitro high throughput screen (HTS) of small molecule compounds and have identified and validated the drug Celastrol as a novel inhibitor of YAP/TAZ–TEAD interaction. We have also demonstrated that Celastrol can inhibit cancer cell proliferation, transformation, and cell migration. In this study, we describe a new inhibitor of the YAP/TAZ–TEAD interaction warranting further investigation and offer a novel biosensor tool for the discovery of other new Hippo-targeting drugs in future work.


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