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YAP/TAZ: Molecular pathway and disease therapy

The Yes‐associated protein and its transcriptional coactivator with PDZ‐binding motif (YAP/TAZ) are two homologous transcriptional coactivators that lie at the center of a key regulatory network of Hippo, Wnt, GPCR, estrogen, mechanical, and metabolism signaling. YAP/TAZ influences the expressions o...

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Autores principales: Wei, Yuzi, Hui, Victoria Lee Zhi, Chen, Yilin, Han, Ruiying, Han, Xianglong, Guo, Yongwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10412783/
https://www.ncbi.nlm.nih.gov/pubmed/37576865
http://dx.doi.org/10.1002/mco2.340
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author Wei, Yuzi
Hui, Victoria Lee Zhi
Chen, Yilin
Han, Ruiying
Han, Xianglong
Guo, Yongwen
author_facet Wei, Yuzi
Hui, Victoria Lee Zhi
Chen, Yilin
Han, Ruiying
Han, Xianglong
Guo, Yongwen
author_sort Wei, Yuzi
collection PubMed
description The Yes‐associated protein and its transcriptional coactivator with PDZ‐binding motif (YAP/TAZ) are two homologous transcriptional coactivators that lie at the center of a key regulatory network of Hippo, Wnt, GPCR, estrogen, mechanical, and metabolism signaling. YAP/TAZ influences the expressions of downstream genes and proteins as well as enzyme activity in metabolic cycles, cell proliferation, inflammatory factor expression, and the transdifferentiation of fibroblasts into myofibroblasts. YAP/TAZ can also be regulated through epigenetic regulation and posttranslational modifications. Consequently, the regulatory function of these mechanisms implicates YAP/TAZ in the pathogenesis of metabolism‐related diseases, atherosclerosis, fibrosis, and the delicate equilibrium between cancer progression and organ regeneration. As such, there arises a pressing need for thorough investigation of YAP/TAZ in clinical settings. In this paper, we aim to elucidate the signaling pathways that regulate YAP/TAZ and explore the mechanisms of YAP/TAZ‐induce diseases and their potential therapeutic interventions. Furthermore, we summarize the current clinical studies investigating treatments targeting YAP/TAZ. We also address the limitations of existing research on YAP/TAZ and propose future directions for research. In conclusion, this review aims to provide fresh insights into the signaling mediated by YAP/TAZ and identify potential therapeutic targets to present innovative solutions to overcome the challenges associated with YAP/TAZ.
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spelling pubmed-104127832023-08-11 YAP/TAZ: Molecular pathway and disease therapy Wei, Yuzi Hui, Victoria Lee Zhi Chen, Yilin Han, Ruiying Han, Xianglong Guo, Yongwen MedComm (2020) Reviews The Yes‐associated protein and its transcriptional coactivator with PDZ‐binding motif (YAP/TAZ) are two homologous transcriptional coactivators that lie at the center of a key regulatory network of Hippo, Wnt, GPCR, estrogen, mechanical, and metabolism signaling. YAP/TAZ influences the expressions of downstream genes and proteins as well as enzyme activity in metabolic cycles, cell proliferation, inflammatory factor expression, and the transdifferentiation of fibroblasts into myofibroblasts. YAP/TAZ can also be regulated through epigenetic regulation and posttranslational modifications. Consequently, the regulatory function of these mechanisms implicates YAP/TAZ in the pathogenesis of metabolism‐related diseases, atherosclerosis, fibrosis, and the delicate equilibrium between cancer progression and organ regeneration. As such, there arises a pressing need for thorough investigation of YAP/TAZ in clinical settings. In this paper, we aim to elucidate the signaling pathways that regulate YAP/TAZ and explore the mechanisms of YAP/TAZ‐induce diseases and their potential therapeutic interventions. Furthermore, we summarize the current clinical studies investigating treatments targeting YAP/TAZ. We also address the limitations of existing research on YAP/TAZ and propose future directions for research. In conclusion, this review aims to provide fresh insights into the signaling mediated by YAP/TAZ and identify potential therapeutic targets to present innovative solutions to overcome the challenges associated with YAP/TAZ. John Wiley and Sons Inc. 2023-08-09 /pmc/articles/PMC10412783/ /pubmed/37576865 http://dx.doi.org/10.1002/mco2.340 Text en © 2023 The Authors. MedComm published by Sichuan International Medical Exchange & Promotion Association (SCIMEA) and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Wei, Yuzi
Hui, Victoria Lee Zhi
Chen, Yilin
Han, Ruiying
Han, Xianglong
Guo, Yongwen
YAP/TAZ: Molecular pathway and disease therapy
title YAP/TAZ: Molecular pathway and disease therapy
title_full YAP/TAZ: Molecular pathway and disease therapy
title_fullStr YAP/TAZ: Molecular pathway and disease therapy
title_full_unstemmed YAP/TAZ: Molecular pathway and disease therapy
title_short YAP/TAZ: Molecular pathway and disease therapy
title_sort yap/taz: molecular pathway and disease therapy
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10412783/
https://www.ncbi.nlm.nih.gov/pubmed/37576865
http://dx.doi.org/10.1002/mco2.340
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