Cyclooxygenase-2 inhibitor NS398 enhances radiosensitivity of radioresistant esophageal cancer cells by inhibiting AKT activation and inducing apoptosis

Cancer Invest. 2010 Aug;28(7):679-88. doi: 10.3109/07357907.2010.483504.

Abstract

This study aimed to evaluate the radiosensitizing effect of a COX-2 inhibitor, NS398, and its mechanism in radioresistant esophageal cancer Eca109R50Gy cells. NS398 enhanced radiosensitivity of Eca109R50Gy cells, characterized by redistribution of cell cycle, inhibition of DNA-dependent protein kinase catalytic subunit expression and induction of apoptosis. NS398 also reduced phospho-AKT level, upregulated expression of Bax and both procaspase-3 and active caspase-3, and downregulated Bcl-2 expression. Finally, NS398-induced radiosensitization was partly reversed by insulin-like growth factor-1, but not by prostaglandin E2. Our results suggest that NS398 may enhance radiosensitivity of Eca109R50Gy cells through blocking AKT activation and inducing apoptosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / drug effects
  • Cell Line, Tumor
  • Cyclooxygenase 2 Inhibitors / pharmacology*
  • Down-Regulation
  • Esophageal Neoplasms
  • Humans
  • Nitrobenzenes / pharmacology*
  • Proto-Oncogene Proteins c-akt / drug effects*
  • Radiation Tolerance
  • Radiation-Sensitizing Agents / pharmacology*
  • Signal Transduction / drug effects
  • Sulfonamides / pharmacology*

Substances

  • Cyclooxygenase 2 Inhibitors
  • Nitrobenzenes
  • Radiation-Sensitizing Agents
  • Sulfonamides
  • N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide
  • Proto-Oncogene Proteins c-akt