Targeting Wnt/β-catenin signaling and its interplay with TGF-β and Notch signaling pathways for the treatment of chronic wounds

Cell Commun Signal. 2024 Apr 26;22(1):244. doi: 10.1186/s12964-024-01623-9.

Abstract

Wound healing is a tightly regulated process that ensures tissue repair and normal function following injury. It is modulated by activation of pathways such as the transforming growth factor-beta (TGF-β), Notch, and Wnt/β-catenin signaling pathways. Dysregulation of this process causes poor wound healing, which leads to tissue fibrosis and ulcerative wounds. The Wnt/β-catenin pathway is involved in all phases of wound healing, primarily in the proliferative phase for formation of granulation tissue. This review focuses on the role of the Wnt/β-catenin signaling pathway in wound healing, and its transcriptional regulation of target genes. The crosstalk between Wnt/β-catenin, Notch, and the TGF-β signaling pathways, as well as the deregulation of Wnt/β-catenin signaling in chronic wounds are also considered, with a special focus on diabetic ulcers. Lastly, we discuss current and prospective therapies for chronic wounds, with a primary focus on strategies that target the Wnt/β-catenin signaling pathway such as photobiomodulation for healing diabetic ulcers.

Keywords: Inflammation; Notch; Photobiomodulation; Signaling Pathway; TGF-β; Wnt/β-catenin; Wound healing.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chronic Disease
  • Humans
  • Receptors, Notch* / metabolism
  • Signal Transduction
  • Transforming Growth Factor beta* / metabolism
  • Wnt Signaling Pathway*
  • Wound Healing*
  • beta Catenin / metabolism

Substances

  • Receptors, Notch
  • Transforming Growth Factor beta
  • beta Catenin