Cimicifuga foetida extract inhibits proliferation of hepatocellular cells via induction of cell cycle arrest and apoptosis

J Ethnopharmacol. 2007 Nov 1;114(2):227-33. doi: 10.1016/j.jep.2007.08.008. Epub 2007 Aug 12.

Abstract

The purpose of this study is to determine whether the ethyl acetate fraction (EAF) from the aerial part of Cimicifuga foetida Linnaeus possesses the anti-tumor action on hepatoma, and therefore, provide evidence for the traditional use of the plant as a detoxification agent. EAF was extracted and its cytotoxicity was evaluated on a panel of Hepatocytes by MTT assay. The IC(50) values of EAF on HepG2, R-HepG2 and primary cultured normal mouse hepatocytes were 21, 43 and 80 microg/mL, respectively. Morphology observation, Annexin V-FITC/PI staining, cell cycle analysis and western blot were used to further elucidate the cytotoxic mechanism of EAF. EAF induced G(0)/G(1)cell cycle arrest at lower concentration (25 microg/mL), and triggered G(2)/M arrest and apoptosis at higher concentrations (50 and 100 microg/mL, respectively). An increase in the ratio of Bax/Bcl-2, activation of downstream effector Caspase 3, and cleavage of poly-ADP-ribose polymerase (PARP) were implicated in EAF-induced apoptosis. In addition, EAF inhibited the growth of the implanted mouse H(22) tumor in a dose-dependent manner with the growth inhibitory rate of 63.32% at 200 mg/kg. In conclusion, EAF may potentially find use as a new therapy for the treatment of hepatoma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Annexin A5 / metabolism
  • Antineoplastic Agents, Phytogenic / pharmacology
  • Apoptosis / drug effects*
  • Apoptosis Regulatory Proteins / metabolism
  • Betulinic Acid
  • Carcinoma, Hepatocellular / drug therapy
  • Carcinoma, Hepatocellular / pathology
  • Cell Cycle / drug effects*
  • Cell Proliferation / drug effects*
  • Cells, Cultured
  • Cimicifuga / chemistry*
  • Dose-Response Relationship, Drug
  • Fluorescein-5-isothiocyanate
  • Fluorescent Dyes
  • Hepatocytes / drug effects*
  • Humans
  • Male
  • Mice
  • Mice, Inbred ICR
  • Neoplasm Transplantation
  • Pentacyclic Triterpenes
  • Plant Extracts / pharmacology
  • Triterpenes / chemistry
  • Triterpenes / isolation & purification
  • Triterpenes / pharmacology
  • Xenograft Model Antitumor Assays

Substances

  • Annexin A5
  • Antineoplastic Agents, Phytogenic
  • Apoptosis Regulatory Proteins
  • Fluorescent Dyes
  • Pentacyclic Triterpenes
  • Plant Extracts
  • Triterpenes
  • Fluorescein-5-isothiocyanate
  • Betulinic Acid