Apoptosis induction by glycoprotein isolated from Laminaria japonica is associated with down-regulation of telomerase activity and prostaglandin E2 synthesis in AGS human gastric cancer cells

Int J Oncol. 2011 Feb;38(2):577-84. doi: 10.3892/ijo.2010.853. Epub 2010 Dec 3.

Abstract

Glycoprotein isolated from Laminaria japonica (LJGP) is known to exhibit significant cytotoxic activity against human cancer cells; however, the mechanisms of its cytoxicity are poorly understood. In this study, we investigated further possible mechanisms by which LJGP exerts its anti-cancer action in cultured human gastric carcinoma AGS cells. LJGP treatment of AGS cells resulted in inhibition of growth and induction of apoptosis in a time- and concentration-dependent manner, as determined by MTT assay, fluorescence microscopy, and flow cytometry analysis. The increase in apoptosis was associated with up-regulation of pro-apoptotic Bax expression, down-regulation of anti-apoptotic Bcl-2 and IAP family members, and activation of caspase-3 and -9. LJGP treatment markedly down-regulated the activity of telomerase and expression of human telomerase reverse transcriptase, a main determinant of telomerase enzymatic activity, with inhibition of Sp1 and c-Myc expression in a concentration-dependent manner. Furthermore, LJGP treatment also caused a progressive decrease in the expression levels of cyclooxygenase (COX)-2 without significant changes in the levels of COX-1, which was correlated with a decrease in prostaglandin E2 synthesis. These results provide important new insights into the possible molecular mechanisms of the anti-cancer activity of LJGP.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis*
  • Blotting, Western
  • Caspase 3 / metabolism
  • Cell Line, Tumor
  • Cyclooxygenase 2 / chemistry
  • Cyclooxygenase 2 / metabolism
  • Dinoprostone / antagonists & inhibitors
  • Dinoprostone / metabolism*
  • Down-Regulation
  • Flow Cytometry
  • Glycoproteins / metabolism*
  • Humans
  • Laminaria / chemistry*
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Stomach Neoplasms / pathology*
  • Telomerase / antagonists & inhibitors*
  • Telomerase / metabolism

Substances

  • Glycoproteins
  • Proto-Oncogene Proteins c-bcl-2
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • TERT protein, human
  • Telomerase
  • Caspase 3
  • Dinoprostone