TGF‑β signaling: A complex role in tumorigenesis (Review)

Mol Med Rep. 2018 Jan;17(1):699-704. doi: 10.3892/mmr.2017.7970. Epub 2017 Nov 6.

Abstract

Tumor progression can be affected by various cellular components of tumor cells and/or by tumor microenvironmental factors. The tumor microenvironment comprises a variety of nonmalignant stromal cells and inflammatory cytokines, which are pivotal in tumor promotion and progression. The transforming growth factor‑β (TGF‑β) ligands (TGF‑β1, 2 and 3) are secreted inflammatory cytokines, which are known to be involved in various aspects of tumor development through two transmembrane serine‑threonine kinase receptors, TGFβR1 and TGFβR2. TGF‑β promotes or inhibits tumorigenesis depending on the concurrent gene mutations and tissue microenvironment present through the small mothers against decapentaplegic (Smad) and non‑Smad pathways. This review aims to provide a comprehensive overview of the role of the TGF‑β pathway in tumor initiation and progression.

Publication types

  • Review

MeSH terms

  • Carcinogenesis / genetics*
  • Humans
  • Neoplasms / genetics*
  • Neoplasms / pathology
  • Protein Serine-Threonine Kinases / genetics
  • Receptor, Transforming Growth Factor-beta Type I
  • Receptor, Transforming Growth Factor-beta Type II
  • Receptors, Transforming Growth Factor beta / genetics
  • Signal Transduction / genetics
  • Stromal Cells / metabolism
  • Stromal Cells / pathology
  • Transforming Growth Factor beta / classification
  • Transforming Growth Factor beta / genetics*
  • Tumor Microenvironment / genetics

Substances

  • Receptors, Transforming Growth Factor beta
  • Transforming Growth Factor beta
  • Protein Serine-Threonine Kinases
  • Receptor, Transforming Growth Factor-beta Type I
  • Receptor, Transforming Growth Factor-beta Type II