Tgf-β signaling: From tissue fibrosis to tumor microenvironment

  • Jeff Yat Fai Chung*
  • , Max Kam Kwan Chan*
  • , Jane Siu Fan Li*
  • , Alex Siu Wing Chan*
  • , Philip Chiu Tsun Tang*
  • , Kam Tong Leung*
  • , Ka Fai To*
  • , Hui Yao Lan*
  • , Patrick Ming Kuen Tang*
  • *Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

163 Citations (Scopus)

Abstract

Transforming growth factor-β (TGF-β) signaling triggers diverse biological actions in inflammatory diseases. In tissue fibrosis, it acts as a key pathogenic regulator for promoting immunoregulation via controlling the activation, proliferation, and apoptosis of immunocytes. In cancer, it plays a critical role in tumor microenvironment (TME) for accelerating invasion, metastasis, angiogenesis, and immunosuppression. Increasing evidence suggest a pleiotropic nature of TGF-β signaling as a critical pathway for generating fibrotic TME, which contains numerous cancer-associated fibroblasts (CAFs), extracellular matrix proteins, and remodeling enzymes. Its pathogenic roles and working mechanisms in tumorigenesis are still largely unclear. Importantly, recent studies successfully demonstrated the clinical implications of fibrotic TME in cancer. This review systematically summarized the latest updates and discoveries of TGF-β signaling in the fibrotic TME.

Original languageEnglish
Article number7575
Number of pages18
JournalInternational Journal of Molecular Sciences
Volume22
Issue number14
DOIs
Publication statusPublished - 15 Jul 2021

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

User-Defined Keywords

  • Fibrosis
  • TGF-β
  • Tumor microenvironment

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