23-hydroxyursolic acid causes cell growth-inhibition by inducing caspase-dependent apoptosis in human cervical squamous carcinoma HeLa cells

Anticancer Res. 2009 Apr;29(4):995-1000.

Abstract

Background: There are few reports on the biological activities of 23-hydroxyursolic acid (23-HUA). The mechanism of growth-inhibition induced by 23-HUA, isolated from Cussonia bancoensis, in human cervical squamous carcinoma HeLa cells is hereby investigated.

Materials and methods: The growth-inhibitory activity was measured by MTS assay. Caspases activation and expression of apoptosis-related proteins were detected by Western blotting. Apoptotic cells were observed by morphological analysis with Hoechst 33342.

Results: 23-HUA inhibited the growth of HeLa cells in a concentration dependent manner. Proteolytically generated fragments of caspase-3, -8 and -9 were observed in HeLa cells treated with 60 microM 23-HUA. The expression of Bcl-X(L), an anti-apoptotic protein, was markedly decreased by 60 microM 23-HUA. Morphological analysis showed that apoptotic changes occurred after treatment with 60 microM 23-HUA, and the changes were inhibited by a pan-caspase inhibitor, Z-VAD-FMK.

Conclusion: These results indicate that 23-HUA causes potent growth-inhibition by the induction of apoptosis via activation of caspases in HeLa cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / drug effects*
  • Blotting, Western
  • Caspases / metabolism*
  • Fas-Associated Death Domain Protein / metabolism
  • Female
  • HeLa Cells / metabolism
  • HeLa Cells / pathology
  • Humans
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Triterpenes / pharmacology*
  • Tumor Cells, Cultured

Substances

  • FADD protein, human
  • Fas-Associated Death Domain Protein
  • Proto-Oncogene Proteins c-bcl-2
  • Triterpenes
  • 23-hydroxyursolic acid
  • Caspases