Ginsenoside-Rh2 blocks the cell cycle of SK-HEP-1 cells at the G1/S boundary by selectively inducing the protein expression of p27kip1

Cancer Lett. 1996 Dec 20;110(1-2):193-200. doi: 10.1016/s0304-3835(96)04502-8.

Abstract

The mechanism of action by which ginsenoside-Rh2 (G-Rh2) suppresses the proliferation of SK-HEP-1 cells is reported. The results from flow cytometric analyses show that G-Rh2 arrested the cell cycle at the G1/S transition phase. The cyclin E-dependent kinase activity which had been immunoprecipitated with cyclin E-specific antibody was down-regulated in the cells in response to G-Rh2. The IC50 value required to down-regulate the kinase activity by 50% was approximately 0.75 microM. Immunoblotting analyses show that G-Rh2 selectively induced the expression of p27kip1 in a dose-dependent manner whereas it had no effect on the levels of cyclin E, cdk2, and p21WAF1. In addition, our data show that G-Rh2 reduced the protein levels of cdc25A at doses higher than 10 microM. Collectively, these data suggest that ginsenoside-Rh2 arrests the cell cycle at the G1/S transition phase by selectively inducing protein expression of p27Kip1 and, as a consequence, down-regulating cyclin E-dependent kinase activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • COS Cells / drug effects
  • COS Cells / metabolism
  • Cell Cycle Proteins*
  • Cyclin-Dependent Kinase Inhibitor p27
  • Cyclin-Dependent Kinases / metabolism*
  • DNA, Neoplasm / biosynthesis
  • DNA, Neoplasm / drug effects
  • Down-Regulation
  • G1 Phase / drug effects
  • Ginsenosides*
  • HeLa Cells / drug effects
  • HeLa Cells / metabolism
  • Humans
  • Liver Neoplasms / metabolism
  • Microtubule-Associated Proteins / metabolism*
  • Rats
  • Saponins / pharmacology*
  • Tumor Cells, Cultured / drug effects
  • Tumor Cells, Cultured / metabolism
  • Tumor Suppressor Proteins*

Substances

  • Cdkn1b protein, rat
  • Cell Cycle Proteins
  • DNA, Neoplasm
  • Ginsenosides
  • Microtubule-Associated Proteins
  • Saponins
  • Tumor Suppressor Proteins
  • Cyclin-Dependent Kinase Inhibitor p27
  • ginsenoside Rh2
  • Cyclin-Dependent Kinases