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Identification of a Quinone Derivative as a YAP/TEAD Activity Modulator from a Repurposing Library
The transcriptional regulators YAP (Yes-associated protein) and TAZ (transcriptional co-activator with PDZ-binding motif) are the major downstream effectors in the Hippo pathway and are involved in cancer progression through modulation of the activity of TEAD (transcriptional enhanced associate doma...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8878929/ https://www.ncbi.nlm.nih.gov/pubmed/35214125 http://dx.doi.org/10.3390/pharmaceutics14020391 |
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author | Lauriola, Angela Uliassi, Elisa Santucci, Matteo Bolognesi, Maria Laura Mor, Marco Scalvini, Laura Elisi, Gian Marco Gozzi, Gaia Tagliazucchi, Lorenzo Marverti, Gaetano Ferrari, Stefania Losi, Lorena D’Arca, Domenico Costi, Maria Paola |
author_facet | Lauriola, Angela Uliassi, Elisa Santucci, Matteo Bolognesi, Maria Laura Mor, Marco Scalvini, Laura Elisi, Gian Marco Gozzi, Gaia Tagliazucchi, Lorenzo Marverti, Gaetano Ferrari, Stefania Losi, Lorena D’Arca, Domenico Costi, Maria Paola |
author_sort | Lauriola, Angela |
collection | PubMed |
description | The transcriptional regulators YAP (Yes-associated protein) and TAZ (transcriptional co-activator with PDZ-binding motif) are the major downstream effectors in the Hippo pathway and are involved in cancer progression through modulation of the activity of TEAD (transcriptional enhanced associate domain) transcription factors. To exploit the advantages of drug repurposing in the search of new drugs, we developed a similar approach for the identification of new hits interfering with TEAD target gene expression. In our study, a 27-member in-house library was assembled, characterized, and screened for its cancer cell growth inhibition effect. In a secondary luciferase-based assay, only seven compounds confirmed their specific involvement in TEAD activity. IA5 bearing a p-quinoid structure reduced the cytoplasmic level of phosphorylated YAP and the YAP–TEAD complex transcriptional activity and reduced cancer cell growth. IA5 is a promising hit compound for TEAD activity modulator development. |
format | Online Article Text |
id | pubmed-8878929 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88789292022-02-26 Identification of a Quinone Derivative as a YAP/TEAD Activity Modulator from a Repurposing Library Lauriola, Angela Uliassi, Elisa Santucci, Matteo Bolognesi, Maria Laura Mor, Marco Scalvini, Laura Elisi, Gian Marco Gozzi, Gaia Tagliazucchi, Lorenzo Marverti, Gaetano Ferrari, Stefania Losi, Lorena D’Arca, Domenico Costi, Maria Paola Pharmaceutics Article The transcriptional regulators YAP (Yes-associated protein) and TAZ (transcriptional co-activator with PDZ-binding motif) are the major downstream effectors in the Hippo pathway and are involved in cancer progression through modulation of the activity of TEAD (transcriptional enhanced associate domain) transcription factors. To exploit the advantages of drug repurposing in the search of new drugs, we developed a similar approach for the identification of new hits interfering with TEAD target gene expression. In our study, a 27-member in-house library was assembled, characterized, and screened for its cancer cell growth inhibition effect. In a secondary luciferase-based assay, only seven compounds confirmed their specific involvement in TEAD activity. IA5 bearing a p-quinoid structure reduced the cytoplasmic level of phosphorylated YAP and the YAP–TEAD complex transcriptional activity and reduced cancer cell growth. IA5 is a promising hit compound for TEAD activity modulator development. MDPI 2022-02-10 /pmc/articles/PMC8878929/ /pubmed/35214125 http://dx.doi.org/10.3390/pharmaceutics14020391 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Lauriola, Angela Uliassi, Elisa Santucci, Matteo Bolognesi, Maria Laura Mor, Marco Scalvini, Laura Elisi, Gian Marco Gozzi, Gaia Tagliazucchi, Lorenzo Marverti, Gaetano Ferrari, Stefania Losi, Lorena D’Arca, Domenico Costi, Maria Paola Identification of a Quinone Derivative as a YAP/TEAD Activity Modulator from a Repurposing Library |
title | Identification of a Quinone Derivative as a YAP/TEAD Activity Modulator from a Repurposing Library |
title_full | Identification of a Quinone Derivative as a YAP/TEAD Activity Modulator from a Repurposing Library |
title_fullStr | Identification of a Quinone Derivative as a YAP/TEAD Activity Modulator from a Repurposing Library |
title_full_unstemmed | Identification of a Quinone Derivative as a YAP/TEAD Activity Modulator from a Repurposing Library |
title_short | Identification of a Quinone Derivative as a YAP/TEAD Activity Modulator from a Repurposing Library |
title_sort | identification of a quinone derivative as a yap/tead activity modulator from a repurposing library |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8878929/ https://www.ncbi.nlm.nih.gov/pubmed/35214125 http://dx.doi.org/10.3390/pharmaceutics14020391 |
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