Regulatory mechanisms for transforming growth factor beta as an autocrine inhibitor in human hepatocellular carcinoma: implications for roles of smads in its growth

Hepatology. 2000 Aug;32(2):218-27. doi: 10.1053/jhep.2000.9145.

Abstract

Transforming growth factor beta (TGF-beta) initiates signaling through heteromeric complexes of transmembrane type I and type II serine/threonine kinase receptors. Activated TGF-beta type I receptor phosphorylates receptor-regulated Smads (2 and 3). Antagonistic Smad 7 forms stable association with the activated TGF-beta type I receptor, blocking phosphorylation of receptor-regulated Smads. On the other hand, elevated serum concentration of TGF-beta along with resistance to its growth-inhibitory effect is commonly observed in human hepatocellular carcinoma (HCC) patients. In this study, we investigated the mechanisms of resistance to tumor-derived TGF-beta in human HCC and hepatoblastoma-derived cell lines, focusing on the roles of receptor-regulated Smads and antagonistic Smad 7. HuH-7 and HepG2 cells showed poor response to TGF-beta-mediated growth inhibition. Because neutralization of TGF-beta in the medium or blockage of signal transduction pathway by inductions of dominant negative Smad 2/3 resulted in a stimulation of cell growth, tumor-derived TGF-beta signal acts on cell growth negatively. However, Smad 7 induced by TGF-beta negatively regulated Smad 2 action and rendered most Smad 2 proteins in the cytoplasm. Taken together, these results indicate that endogenous TGF-beta-mediated induction of Smad 7 results in a higher "threshold" for the antiproliferative signals mediated by receptor-regulated Smads, and can be involved in reduced responsiveness to the cytokine in some human HCC cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinoma, Hepatocellular / pathology*
  • Cell Cycle Proteins*
  • Cyclin-Dependent Kinase Inhibitor p15
  • DNA-Binding Proteins / physiology*
  • Humans
  • Liver Neoplasms / pathology*
  • Phosphorylation
  • Plasminogen Activator Inhibitor 1 / genetics
  • RNA, Messenger / analysis
  • Receptor, IGF Type 2 / analysis
  • Smad2 Protein
  • Smad3 Protein
  • Smad7 Protein
  • Trans-Activators / physiology*
  • Transcription Factors / physiology
  • Transforming Growth Factor beta / genetics
  • Transforming Growth Factor beta / physiology*
  • Tumor Cells, Cultured
  • Tumor Suppressor Proteins*

Substances

  • CDKN2B protein, human
  • Cell Cycle Proteins
  • Cyclin-Dependent Kinase Inhibitor p15
  • DNA-Binding Proteins
  • Plasminogen Activator Inhibitor 1
  • RNA, Messenger
  • Receptor, IGF Type 2
  • SMAD2 protein, human
  • SMAD3 protein, human
  • SMAD7 protein, human
  • Smad2 Protein
  • Smad3 Protein
  • Smad7 Protein
  • Trans-Activators
  • Transcription Factors
  • Transforming Growth Factor beta
  • Tumor Suppressor Proteins