Anti-proliferative Effect of Coptis Chinensis Extract in Hep G2 Cells

  • Kim, Jun-Lae (Department of East-West Cancer Center, Dunsan Oriental Hospital of Daejeon University) ;
  • Oh, Se-Mi (Department of East-West Cancer Center, Dunsan Oriental Hospital of Daejeon University) ;
  • Shin, Jang-Woo (Department of East-West Cancer Center, Dunsan Oriental Hospital of Daejeon University) ;
  • Son, Jin-Young (Department of East-West Cancer Center, Dunsan Oriental Hospital of Daejeon University) ;
  • Cho, Jung-Hyo (Department of East-West Cancer Center, Dunsan Oriental Hospital of Daejeon University) ;
  • Lee, Yeon-Weol (Department of East-West Cancer Center, Dunsan Oriental Hospital of Daejeon University) ;
  • Son, Chang-Gue (Department of East-West Cancer Center, Dunsan Oriental Hospital of Daejeon University) ;
  • Cho, Chong-Kwan (Department of East-West Cancer Center, Dunsan Oriental Hospital of Daejeon University) ;
  • Yoo, Hwa-Seung (Department of East-West Cancer Center, Dunsan Oriental Hospital of Daejeon University)
  • Published : 2006.12.30

Abstract

Objectives : This study is aimed to elucidate anti-hepatoma activity of Coptis Chinensis Extract (CCE) and evaluate its effect on proliferation of human hepatoma Hep G2 cells. Methods : To identify CCE and control the quality, we performed fingerprinting by high-performance thin layer chromatography (HPTLC). To investigate effects of CCE on anti-hepatoma activity, we measured cytotoxicity against Hep G2 cells compared with treatment of paclitaxel and 5-fluorouracil (5-FU). To examine the mechanism of inhibitory effect of CCE on Hep G2 cell proliferation, cell cycle distribution was evaluated using fluorescent activated cell sorter (FACS) Result : CCE showed a significant effect that arrests Hep G2 cells at the G2/M phase of the cell cycle. CCE combined with paclitaxel inhibited synergistically cell growth of Hep G2 cells. Conclusion : CCE may present anticancer effects through inhibition of hepatocellular carcinoma (HCC) cell proliferation via G2/M arrest, and may be a useful anticancer agent for HCC.

Keywords