Evodiamine, a constituent of Evodiae Fructus, induces anti-proliferating effects in tumor cells

Cancer Sci. 2003 Jan;94(1):92-8. doi: 10.1111/j.1349-7006.2003.tb01358.x.

Abstract

We found that evodiamine, a major alkaloidal component of Evodiae Fructus (Goshuyu in Japan), inhibited proliferation of several tumor cell lines, but had less effect on human peripheral blood mononuclear cells (PBMC). We used human cervical cancer cells, HeLa, as a model to elucidate the molecular mechanisms of evodiamine-induced tumor cell death. The results showed that evodiamine induced oligonucleosomal fragmentation of DNA in HeLa cells and increased the activity of caspase-3, but not that of caspase-1, in vitro. Both evodiamine-induced DNA fragmentation and caspase-3 activity were effectively inhibited by a caspase-3 inhibitor, z-DEVD-fmk (z-Asp-Glu-Val-Asp-fmk). In addition, evodiamine increased the expression of the apoptosis inducer Bax, but decreased the expression of the apoptosis suppressor Bcl-2 in mitochondria. Taken together, our data indicated that evodiamine alters the balance of Bcl-2 and Bax gene expression and induces apoptosis through the caspase pathway in HeLa cells.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaloids / chemistry
  • Alkaloids / pharmacology
  • Amino Acid Chloromethyl Ketones / pharmacology
  • Animals
  • Antineoplastic Agents, Phytogenic / pharmacology*
  • Apoptosis / drug effects*
  • Caspase 3
  • Caspases / metabolism
  • Cell Division / drug effects
  • Cysteine Proteinase Inhibitors / pharmacology
  • DNA Fragmentation / drug effects
  • Dactinomycin / pharmacology
  • Drug Screening Assays, Antitumor
  • Enzyme Activation / drug effects
  • Evodia / chemistry*
  • Fibrosarcoma / pathology
  • Fluorouracil / pharmacology
  • Furans / chemistry
  • Furans / pharmacology
  • Gene Expression Regulation, Neoplastic / drug effects
  • Genes, bcl-2 / drug effects
  • HeLa Cells / drug effects
  • HeLa Cells / enzymology
  • Hepatocytes / drug effects
  • Heterocyclic Compounds, 4 or More Rings / chemistry
  • Heterocyclic Compounds, 4 or More Rings / pharmacology
  • Humans
  • Indole Alkaloids
  • Leukemia, Monocytic, Acute / pathology
  • Leukocytes, Mononuclear / drug effects
  • Melanoma / pathology
  • Mice
  • Mitochondria / drug effects
  • Molecular Structure
  • Neoplasm Proteins / metabolism
  • Oligopeptides / pharmacology
  • Plant Extracts / chemistry
  • Plant Extracts / pharmacology*
  • Proto-Oncogene Proteins / biosynthesis
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins c-bcl-2 / biosynthesis
  • Quinazolines / chemistry
  • Quinazolines / pharmacology*
  • Rats
  • Rats, Inbred BUF
  • Sarcoma 180 / pathology
  • Tumor Cells, Cultured / drug effects*
  • Tumor Cells, Cultured / enzymology
  • bcl-2-Associated X Protein

Substances

  • Alkaloids
  • Amino Acid Chloromethyl Ketones
  • Antineoplastic Agents, Phytogenic
  • BAX protein, human
  • Bax protein, mouse
  • Bax protein, rat
  • Cysteine Proteinase Inhibitors
  • Furans
  • Heterocyclic Compounds, 4 or More Rings
  • Indole Alkaloids
  • Neoplasm Proteins
  • Oligopeptides
  • Plant Extracts
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • Quinazolines
  • bcl-2-Associated X Protein
  • benzoylcarbonyl-aspartyl-glutamyl-valyl-aspartyl-fluoromethyl ketone
  • benzyloxycarbonylvalyl-alanyl-aspartyl fluoromethyl ketone
  • evodine
  • Dactinomycin
  • rutecarpine
  • evodiamine
  • CASP3 protein, human
  • Casp3 protein, mouse
  • Casp3 protein, rat
  • Caspase 3
  • Caspases
  • Fluorouracil