Reverse correlation of Jab1 and Smad4 in PANC-1 cells involved in the pathogenesis of pancreatic cancer

Int J Clin Exp Pathol. 2015 Aug 1;8(8):9279-85. eCollection 2015.

Abstract

Objective: Steps in the genetic basis of pancreatic cancer (PC) have been recently identified, however, Studies focusing on the relationship between Jab1 and Smad4 in PC are rarely reported. This study was performed to examine the expression patterns and association of Jab1 and Smad4 in PC cells for gaining a further understanding of PC pathogenesis.

Methods: Human pancreatic cancer cell line PANC-1 cells were infected with retrovirus vector containing GFP, HA-Jab1, siGFP, and siJab1 respectively. The expression of Jab1 and Smad4 in PANC-1 cells was analyzed by Western blot and immunocytochemistry. Subsequently, the effect of overexpression of Jab1 on cell proliferation inhibition mediated by TGF-β was examined with MTT colorimetry.

Results: The expression of Smad4 in PANC-1 cells was inhibited after the overexpression of Jab1. Inversely, the expression of Smad4 was increased after the down-regulation of Jab1 silenced by SiRNA. Smad4 expression in PANC-1 cells was negatively correlated with Jab1 expression. In addition, the cell proliferation inhibitory effect induced by TGF-β in PANC-1 cells was attenuated after the overexpression of Jab1.

Conclusions: The reverse correlation of Jab1 and Smad4 in PANC-1 cells may be involved in the Pathogenesis of PC. Jab1 can cause degradation of Smad4 via TGF-β signal pathway, consequently contributing to the proliferation of PC cells.

Keywords: Jab1; Smad4; TGF-β; pancreatic cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • COP9 Signalosome Complex
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cell Proliferation / genetics
  • Humans
  • Intracellular Signaling Peptides and Proteins / genetics
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Pancreatic Neoplasms / genetics
  • Pancreatic Neoplasms / metabolism*
  • Pancreatic Neoplasms / pathology
  • Peptide Hydrolases / genetics
  • Peptide Hydrolases / metabolism*
  • Signal Transduction / drug effects
  • Signal Transduction / genetics
  • Smad4 Protein / genetics
  • Smad4 Protein / metabolism*
  • Transforming Growth Factor beta / pharmacology

Substances

  • Intracellular Signaling Peptides and Proteins
  • Smad4 Protein
  • Transforming Growth Factor beta
  • Peptide Hydrolases
  • COPS5 protein, human
  • COP9 Signalosome Complex