TGF-β Signaling in Liver, Pancreas, and Gastrointestinal Diseases and Cancer

Gastroenterology. 2021 Aug;161(2):434-452.e15. doi: 10.1053/j.gastro.2021.04.064. Epub 2021 Apr 30.

Abstract

Genetic alterations affecting transforming growth factor-β (TGF-β) signaling are exceptionally common in diseases and cancers of the gastrointestinal system. As a regulator of tissue renewal, TGF-β signaling and the downstream SMAD-dependent transcriptional events play complex roles in the transition from a noncancerous disease state to cancer in the gastrointestinal tract, liver, and pancreas. Furthermore, this pathway also regulates the stromal cells and the immune system, which may contribute to evasion of the tumors from immune-mediated elimination. Here, we review the involvement of the TGF-β pathway mediated by the transcriptional regulators SMADs in disease progression to cancer in the digestive system. The review integrates human genomic studies with animal models that provide clues toward understanding and managing the complexity of the pathway in disease and cancer.

Keywords: Cancers; Digestive System; Transforming Growth Factor–β.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Digestive System Neoplasms / genetics
  • Digestive System Neoplasms / metabolism*
  • Digestive System Neoplasms / pathology
  • Disease Progression
  • Gastrointestinal Diseases / genetics
  • Gastrointestinal Diseases / metabolism*
  • Gastrointestinal Diseases / pathology
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Liver Diseases / genetics
  • Liver Diseases / metabolism*
  • Liver Diseases / pathology
  • Pancreatic Diseases / genetics
  • Pancreatic Diseases / metabolism*
  • Pancreatic Diseases / pathology
  • Receptors, Transforming Growth Factor beta / genetics
  • Receptors, Transforming Growth Factor beta / metabolism*
  • Signal Transduction
  • Smad Proteins / genetics
  • Smad Proteins / metabolism*
  • Transforming Growth Factor beta / genetics
  • Transforming Growth Factor beta / metabolism*
  • Tumor Microenvironment

Substances

  • Receptors, Transforming Growth Factor beta
  • Smad Proteins
  • Transforming Growth Factor beta