Signaling components involved in Bcl-w-induced migration of gastric cancer cells

Cancer Lett. 2009 May 8;277(1):22-8. doi: 10.1016/j.canlet.2008.11.022. Epub 2008 Dec 20.

Abstract

We have previously reported that Bcl-w enhances the invasiveness of gastric cancer cells by inducing MMP-2 expression via phosphoinositide 3-kinase (PI3K), Akt and Sp1. This study demonstrates that Bcl-w additionally induces uPA expression and FAK activation. Analyses of the hierarchical relationship and functions of these components showed that the PI3K-Akt-Sp1 pathway also mediates the induction of uPA, and that both uPA and MMP-2 contribute to Bcl-w-induced invasion via the stimulation of the FAK-dependent migratory pathway. These findings significantly advance our understandings of the Bcl-w-induced signaling processes that results in the migration and invasion of cancer cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis Regulatory Proteins / physiology*
  • Cell Line, Tumor
  • Cell Movement
  • Focal Adhesion Protein-Tyrosine Kinases / physiology
  • Humans
  • Matrix Metalloproteinase 2 / physiology
  • Phosphatidylinositol 3-Kinases / physiology
  • Proto-Oncogene Proteins c-akt / physiology
  • Signal Transduction / physiology*
  • Sp1 Transcription Factor / physiology
  • Stomach Neoplasms / pathology*
  • Urokinase-Type Plasminogen Activator / physiology

Substances

  • Apoptosis Regulatory Proteins
  • BCL2L2 protein, human
  • Sp1 Transcription Factor
  • Phosphatidylinositol 3-Kinases
  • Focal Adhesion Protein-Tyrosine Kinases
  • Proto-Oncogene Proteins c-akt
  • Urokinase-Type Plasminogen Activator
  • Matrix Metalloproteinase 2