Oncogenic H-Ras and PI3K signaling can inhibit E-cadherin-dependent apoptosis and promote cell survival after photodynamic therapy in mouse keratinocytes

J Cell Physiol. 2009 Apr;219(1):84-93. doi: 10.1002/jcp.21652.

Abstract

Maintenance of E-cadherin mediated cell-cell contacts is often required for the survival of epithelial cells and tissues. Here we report that oncogenic activation of H-Ras in murine keratinocytes can prevent cell death induced by immunological disruption of E-cadherin adhesion. A similar situation was observed in cells showing constitutive activation of the p110 alpha catalytic subunit of class IA PI3K. This protective effect is associated with beta-catenin-dependent transcription and with activation of survival factor Akt/PKB. In addition, we induced cell death by employing photodynamic therapy, using Zn-phthalocyanine as a photosensitizer that targets E-cadherin adhesion complexes. We have found that cell death based on this photodynamic action is also bypassed in cells showing constitutive activation of H-Ras and p110 alpha. Taken together, these results indicate that H-Ras/PI3K/Akt signaling plays a key role in cell survival mediated by E-cadherin cell-cell contacts.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / physiology*
  • Cadherins / genetics
  • Cadherins / metabolism*
  • Cell Cycle / physiology
  • Cell Line
  • Cell Survival / physiology*
  • Enzyme Activation
  • Indoles / metabolism
  • Intercellular Junctions / metabolism
  • Isoindoles
  • Keratinocytes / cytology
  • Keratinocytes / physiology*
  • Keratinocytes / radiation effects*
  • Mice
  • Mice, Inbred BALB C
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Photochemotherapy*
  • Proto-Oncogene Proteins c-akt / metabolism
  • Proto-Oncogene Proteins p21(ras) / genetics
  • Proto-Oncogene Proteins p21(ras) / metabolism*
  • Radiation-Sensitizing Agents / metabolism
  • Signal Transduction

Substances

  • Cadherins
  • Indoles
  • Isoindoles
  • Radiation-Sensitizing Agents
  • Proto-Oncogene Proteins c-akt
  • Proto-Oncogene Proteins p21(ras)
  • phthalocyanine