Matrine induces apoptosis in gastric carcinoma cells via alteration of Fas/FasL and activation of caspase-3

J Ethnopharmacol. 2009 May 4;123(1):91-6. doi: 10.1016/j.jep.2009.02.022. Epub 2009 Mar 3.

Abstract

Aim of the study: Matrine, an alkaloid purified from the chinese herb Sophora flavescens Ait, is well known to possess activities including anti-inflammation, anti-fibrotic and anticancer. In this study, the mechanism of matrine inducing the apoptosis of gastric carcinoma cells was investigated.

Materials and methods: Proliferation of SGC-7901 cells was examined by MTT assay. Cellular morphology was observed under transmission electron microscope. Flow cytometry (FCM) was used to observe the apoptosis of SGC-7901 cells by staining with annexinV-FITC/PI. The expression levels of Fas/FasL in SGC-7901 cells were monitored by FCM analysis using an indirect immunofluorescence method. Activity of caspase-3 enzyme was measured by spectrofluorometry.

Results: MTT assay showed that matrine inhibited SGC-7901 cells proliferation in a dose-dependent and time-dependent manner. Apoptosis induction was demonstrated by morphological changes under electron microscope and FCM analysis. Fluorescence intensity levels of Fas and FasL were found to be equally up-regulated after matrine treatment, which were both correlated with apoptosis rate. The activity of caspase-3 enzyme increased in matrine groups, positively correlated with apoptosis rate.

Conclusions: Matrine could inhibit cell proliferation and induce apoptosis of SGC-7901 cells in vitro. The apoptosis induction appears to proceed by up-regulating Fas/FasL expression and activating caspase-3 enzyme.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaloids / pharmacology*
  • Apoptosis / drug effects*
  • Caspase 3 / metabolism*
  • Cell Line, Tumor
  • Enzyme Activation
  • Fas Ligand Protein / metabolism*
  • Flow Cytometry
  • Fluorescent Antibody Technique
  • Humans
  • Matrines
  • Microscopy, Electron, Transmission
  • Quinolizines / pharmacology*
  • Stomach Neoplasms / enzymology
  • Stomach Neoplasms / metabolism
  • Stomach Neoplasms / pathology*
  • Stomach Neoplasms / ultrastructure
  • fas Receptor / metabolism*

Substances

  • Alkaloids
  • Fas Ligand Protein
  • Quinolizines
  • fas Receptor
  • Caspase 3
  • Matrines