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Wnt/beta-catenin modulation: A promising frontier in chronic kidney disease management.

Authors :
Saxena S
Dagar N
Shelke V
Puri B
Gaikwad AB
Source :
Fundamental & clinical pharmacology [Fundam Clin Pharmacol] 2024 Dec; Vol. 38 (6), pp. 1020-1030. Date of Electronic Publication: 2024 Aug 05.
Publication Year :
2024

Abstract

Background: Being amongst the leading factors of death and distress, chronic kidney disease (CKD) has affected around 850 million people globally. The Wnt/β-catenin axis is vital for maintaining kidney homeostasis, from nephron generation to overall management. The β-catenin growth factor is typically not expressed in the adult kidney; however, its expression is found to increase under stress and injury conditions. It is categorised as canonical and non-canonical based on β-catenin availability, which mounts promising targets for ameliorating CKD. Hence, modulation of the Wnt/β-catenin signalling for CKD management is of utmost relevance.<br />Objectives: The primary aim of this review is to highlight the significance of targeting Wnt/β-catenin signalling for CKD management.<br />Methods: The literature review regarding the role of Wnt/β-catenin signalling and therapies modulating it in CKD was conducted using PubMed, Scopus, Science Direct and Google Scholar.<br />Results: The current review summarises the pharmacological therapies modulating the Wnt/β-catenin axis in CKD, building upon promising preclinical studies to establish a foundation for clinical studies in the future.<br />Conclusion: Wnt/β-catenin signalling is the evolution's most conserved pathway, which plays a pivotal role in CKD progression. Therapies modulating Wnt/β-catenin signalling have emerged as effective means for alleviating CKD.<br /> (© 2024 Société Française de Pharmacologie et de Thérapeutique. Published by John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1472-8206
Volume :
38
Issue :
6
Database :
MEDLINE
Journal :
Fundamental & clinical pharmacology
Publication Type :
Academic Journal
Accession number :
39102849
Full Text :
https://doi.org/10.1111/fcp.13031