Literature DB >> 34510305

WNT Signalling in Osteoarthritis and Its Pharmacological Targeting.

Anna De Palma1, Giovanna Nalesso2.   

Abstract

Osteoarthritis (OA) is a highly disabling musculoskeletal condition affecting millions of people worldwide. OA is characterised by progressive destruction and irreversible morphological changes of joint tissues and architecture. At molecular level, de-regulation of several pathways contributes to the disruption of tissue homeostasis in the joint. Overactivation of the WNT/β-catenin signalling pathway has been associated with degenerative processes in OA. However, the multiple layers of complexity in the modulation of the signalling and the still insufficient knowledge of the specific molecular drivers of pathogenetic mechanisms have made difficult the pharmacological targeting of this pathway for therapeutic purposes. This review aims to provide an overview of the WNT/β-catenin signalling in OA with a particular focus on its role in the articular cartilage. Pathway components whose targeting showed therapeutic potential will be highlighted and described. A specific section will be dedicated to Lorecivivint, the first inhibitor of the β-catenin-dependent pathway currently in phase III clinical trial as OA-modifying agent.
© 2021. The Author(s), under exclusive license to Springer Nature Switzerland AG.

Entities:  

Keywords:  Lorecivivint; Osteoarthritis; Pharmacological targets; WNT signalling

Mesh:

Year:  2021        PMID: 34510305     DOI: 10.1007/164_2021_525

Source DB:  PubMed          Journal:  Handb Exp Pharmacol        ISSN: 0171-2004


  88 in total

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  1 in total

1.  Dickkopf‑3 and β‑catenin play opposite roles in the Wnt/β‑catenin pathway during the abnormal subchondral bone formation of human knee osteoarthritis.

Authors:  Xuegang Liang; Qunhua Jin; Xiaochun Yang; Wenhui Jiang
Journal:  Int J Mol Med       Date:  2022-02-09       Impact factor: 4.101

  1 in total

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