Smad4 is essential for down-regulation of E-cadherin induced by TGF-beta in pancreatic cancer cell line PANC-1

J Biochem. 2007 Mar;141(3):345-51. doi: 10.1093/jb/mvm039. Epub 2007 Feb 14.

Abstract

Smad4 is a tumour suppressor gene frequently deleted in pancreatic cancer. To investigate the roles of Smad4 deficiency in invasive and matastatic capabilities of pancreatic cancer, we examined the effects of Smad4 deficiency on regulation of the invasion suppressor E-cadherin in pancreatic cancer cell line PANC-1. TGF-beta decreased expression of E-cadherin and beta-catenin proteins at the plasma membrane, increased Snail and Slug mRNA expression, and induced fibroblastoid morphology in PANC-1 cells. These effects of TGF-beta were abrogated in Smad4-knocked-down PANC-1 cells. We also found that TGF-beta-induced down-regulation of E-cadherin expression was partially inhibited in Snail- and Slug-knocked-down PANC-1 cells. Thus, Smad4 mediates down-regulation of E-cadherin induced by TGF-beta in PANC-1 cells, at least in part, through Snail and Slug induction. These results suggest that Smad4 deficiency observed in invasive and metastatic pancreatic cancer might not be linked to the loss of E-cadherin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cadherins / biosynthesis*
  • Cell Line, Tumor
  • Down-Regulation
  • Humans
  • Pancreatic Neoplasms / metabolism*
  • Smad3 Protein / deficiency
  • Smad4 Protein / deficiency
  • Smad4 Protein / physiology*
  • Snail Family Transcription Factors
  • Transcription Factors / deficiency
  • Transforming Growth Factor beta / biosynthesis
  • Transforming Growth Factor beta / pharmacology*
  • Vascular Endothelial Growth Factor A / biosynthesis

Substances

  • Cadherins
  • SMAD3 protein, human
  • SMAD4 protein, human
  • SNAI1 protein, human
  • Smad3 Protein
  • Smad4 Protein
  • Snail Family Transcription Factors
  • Transcription Factors
  • Transforming Growth Factor beta
  • VEGFA protein, human
  • Vascular Endothelial Growth Factor A