Growth inhibition and induction of apoptosis in MCF-7 breast cancer cells by Antrodia camphorata

Cancer Lett. 2006 Jan 18;231(2):215-27. doi: 10.1016/j.canlet.2005.02.004.

Abstract

Antrodia camphorata (A. camphorata) is well known in Taiwan as a traditional Chinese medicine, and it has been shown to exhibit antioxidant and anticancer effects. In this study, therefore, its ability to induce apoptosis in cultured MCF-7 breast cancer cells was studied. Treatment of the MCF-7 cells with a variety of concentrations of the fermented culture broth of A. camphorata (25-150 microg/ml) resulted in dose- and time-dependent sequences of events marked by apoptosis, as shown by loss of cell viability, chromatin condensation, internucleosomal DNA fragmentation, and sub-G1 phase accumulation. Furthermore, apoptosis in the MCF-7 cells was accompanied by the release of cytochrome c, activation of caspase 3, and specific proteolytic cleavage of poly (ADP-ribose) polymerase (PARP). Although, the A. camphorata-induced apoptosis was associated with Bax protein levels, negligible Bcl-2 reduction was observed. Interestingly, A. camphorata induced dose-dependent reactive oxygen species (ROS) generation in MCF-7 cells. Analysis of the data suggests that A. camphorata exerts antiproliferative action and growth inhibition on MCF-7 cells through apoptosis induction, and that it may have anticancer properties valuable for application in drug products.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Annexin A5 / metabolism
  • Apoptosis / drug effects*
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / pathology
  • Caspases / metabolism
  • Cell Proliferation / drug effects
  • Cytochromes c / metabolism
  • Dose-Response Relationship, Drug
  • Drugs, Chinese Herbal / therapeutic use*
  • Female
  • Flow Cytometry
  • G1 Phase / drug effects*
  • Humans
  • Poly(ADP-ribose) Polymerases / metabolism
  • Polyporales / chemistry*
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Reactive Oxygen Species / metabolism*
  • Tumor Cells, Cultured
  • bcl-2-Associated X Protein / metabolism

Substances

  • Annexin A5
  • Drugs, Chinese Herbal
  • Proto-Oncogene Proteins c-bcl-2
  • Reactive Oxygen Species
  • bcl-2-Associated X Protein
  • Cytochromes c
  • Poly(ADP-ribose) Polymerases
  • Caspases