YAP/TAZ as master regulators in liver regeneration and disease: insights into mechanisms and therapeutic targets
- PMID: 39718664
- DOI: 10.1007/s11033-024-10177-5
YAP/TAZ as master regulators in liver regeneration and disease: insights into mechanisms and therapeutic targets
Abstract
Yes-associated protein (YAP) and transcriptional coactivator with PDZ-binding motif (TAZ) are key downstream effectors of the Hippo pathway that regulate organ size, tissue homeostasis, and cancer development. YAP/TAZ play crucial regulatory roles in organ growth, cell proliferation, cell renewal, and regeneration. Mechanistically, YAP/TAZ influence the occurrence and progression of liver regeneration (LR) through various signaling pathways, including Notch, Wnt/β-catenin, TGF-β/Smad. While the activation of YAP/TAZ can promote the regeneration of damaged liver tissue, their mechanisms of action may differ under various LR conditions. Furthermore, excessive activation of YAP/TAZ may also lead to severe liver damage, manifesting as alcoholic hepatitis, liver fibrosis, and even liver cancer. Here, we review the role and mechanisms of YAP/TAZ in LR and liver disease, highlighting the potential for advancements in clinical diagnosis and treatment targeting YAP/TAZ in these contexts.
Keywords: Liver disease; Liver regeneration; TAZ; YAP.
© 2024. The Author(s), under exclusive licence to Springer Nature B.V.
Conflict of interest statement
Declarations. Conflict of interest: The author declares that no competing interests. Ethics approval: Not applicable.
Similar articles
-
The effects of YAP/TAZ in cardiomyocytes: a scoping review.Mol Biol Rep. 2025 Apr 15;52(1):392. doi: 10.1007/s11033-025-10492-5. Mol Biol Rep. 2025. PMID: 40232357
-
Proliferation of hepatic stellate cells, mediated by YAP and TAZ, contributes to liver repair and regeneration after liver ischemia-reperfusion injury.Am J Physiol Gastrointest Liver Physiol. 2018 Apr 1;314(4):G471-G482. doi: 10.1152/ajpgi.00153.2017. Epub 2018 Jan 11. Am J Physiol Gastrointest Liver Physiol. 2018. PMID: 29351389 Free PMC article.
-
Suppression of YAP/TAZ-Notch1-NICD axis by bromodomain and extraterminal protein inhibition impairs liver regeneration.Theranostics. 2019 May 31;9(13):3840-3852. doi: 10.7150/thno.33370. eCollection 2019. Theranostics. 2019. PMID: 31281517 Free PMC article.
-
Interplay between YAP/TAZ and metabolic dysfunction-associated steatotic liver disease progression.Arch Pharm Res. 2024 Jun;47(6):558-570. doi: 10.1007/s12272-024-01501-5. Epub 2024 Jun 14. Arch Pharm Res. 2024. PMID: 38874747 Free PMC article. Review.
-
Role of Hippo-YAP/TAZ signaling pathway in organ fibrosis.Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2024 Sept 28;49(9):1509-1516. doi: 10.11817/j.issn.1672-7347.2024.230577. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2024. PMID: 39931781 Free PMC article. Review. Chinese, English.
Cited by
-
[Research Advances in Targeting the YAP/TAZ Signaling Pathway to Improve Cancer Immunotherapy].Zhongguo Fei Ai Za Zhi. 2025 Mar 20;28(3):221-229. doi: 10.3779/j.issn.1009-3419.2025.102.08. Zhongguo Fei Ai Za Zhi. 2025. PMID: 40210482 Free PMC article. Review. Chinese.
-
From Quiescence to Activation: The Reciprocal Regulation of Ras and Rho Signaling in Hepatic Stellate Cells.Cells. 2025 May 5;14(9):674. doi: 10.3390/cells14090674. Cells. 2025. PMID: 40358198 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources