Upregulated expression of periostin by hypoxia in non-small-cell lung cancer cells promotes cell survival via the Akt/PKB pathway

Cancer Lett. 2009 Aug 28;281(2):213-9. doi: 10.1016/j.canlet.2009.02.030. Epub 2009 Mar 27.

Abstract

Periostin is a secreted protein and has been shown to be frequently overexpressed in various types of human cancers. We have previously reported that periostin potently promotes metastatic growth of colon cancer by augmenting cell survival. However, little is known about the functions of periostin in non-small-cell lung cancer. Here, we revealed that increased expression of periostin in non-small-cell lung cancer A549 cells was one kind of cellular responses to the stress of chemical-mimic hypoxia, and this effect could be regulated by hypoxia inducible growth factors, such as TGF-alpha and bFGF. We further demonstrated that RTK/PI3-K pathway activated by TGF-alpha and bFGF was evoked in upregulating the expression of periostin, and then periostin promoted the survival of A549 cells under hypoxic microenvironment via activation of Akt/PKB pathway. Therefore, periostin and the pathway that it involved might provide a target for lung cancer treatment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / physiology
  • Blotting, Western
  • Carcinoma, Non-Small-Cell Lung / metabolism*
  • Cell Adhesion Molecules / metabolism*
  • Cell Hypoxia / physiology*
  • Cell Line, Tumor
  • Cell Survival / physiology
  • Fibroblast Growth Factor 2 / metabolism
  • Humans
  • Lung Neoplasms / metabolism*
  • Proto-Oncogene Proteins c-akt / metabolism
  • Signal Transduction / physiology
  • Transfection
  • Transforming Growth Factor alpha / metabolism
  • Up-Regulation

Substances

  • Cell Adhesion Molecules
  • POSTN protein, human
  • Transforming Growth Factor alpha
  • Fibroblast Growth Factor 2
  • Proto-Oncogene Proteins c-akt