Caspase-independent death of human osteosarcoma cells by flavonoids is driven by p53-mediated mitochondrial stress and nuclear translocation of AIF and endonuclease G

Apoptosis. 2007 Jul;12(7):1289-98. doi: 10.1007/s10495-007-0056-x.

Abstract

Flavonoids have antioxidant and antitumor promoting effects. Rhus verniciflua Stokes (RVS) is a flavonoid-rich herbal medicine that has long been used in Korea as both a food additive and antitumor agent. It was previous reported that a purified flavonoid fraction prepared from RVS, herein named RCMF (the RVS chloroform-methanol fraction), inhibited the proliferation and induced apoptosis in human osteosarcoma (HOS) cells. This study examined the mechanisms involved in the RCMF-mediated apoptosis in HOS cells. RCMF was shown to be capable of inducing apoptosis in HOS cells by inducing p53 in the cells resulting in the decrease in Bcl-2 level, activation of Bax, and cytoplasmic release of cytochrome c, which led to the translocation of apoptosis-inducing factor (AIF) and endonuclease G (EndoG) into the nucleus. However, the RCMF-induced apoptosis was suppressed by transfecting the cells with antisense p53 oligonucleotides but not by treating them with a MAPK or caspase inhibitor. This suppression occurred through the regulation of Bcl-2 members as well as by preventing the nuclear translocation of the mitochondrial apoptogenic factors. Overall, it appears that p53-mediated mitochondrial stress and the nuclear translocation of AIF and EndoG are mainly required for the apoptosis induced by RCMF.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / physiology*
  • Apoptosis Inducing Factor / metabolism*
  • Caspases / metabolism
  • Cell Line, Tumor / cytology
  • Cell Line, Tumor / metabolism*
  • Endodeoxyribonucleases / metabolism*
  • Flavonoids
  • Humans
  • Korea
  • Membrane Potential, Mitochondrial
  • Mitochondria / metabolism*
  • Mitogen-Activated Protein Kinases / metabolism
  • Osteosarcoma
  • Rhus
  • Tumor Suppressor Protein p53 / metabolism*

Substances

  • Apoptosis Inducing Factor
  • Flavonoids
  • Tumor Suppressor Protein p53
  • Mitogen-Activated Protein Kinases
  • Endodeoxyribonucleases
  • endonuclease G
  • Caspases