Doxorubicin and selenium cooperatively induce fas signaling in the absence of Fas/Fas ligand interaction

Anticancer Res. 2007 Sep-Oct;27(5A):3075-82.

Abstract

Background: The synergistic effect of doxorubicin and selenium in apoptosis induction in MCF-7 breast cancer cells has been previously reported. Mitochondrial activation of caspase-9 is in part responsible for the synergy. The present study aimed at examining the death receptor pathway in activating caspase-8 by the two-drug combination.

Materials and methods: We determined the expression of TRAIL and FasL signaling molecules and monitored activated caspase-8 in response to neutralizing/blocking antibodies against ligands/receptors.

Results: Our data suggest that TRAIL signaling might not play a role. With respect to the Fas pathway, it was found that doxorubicin enhanced Fas oligomerization (i.e. activation) independent of FasL-Fas interaction. Selenium, on the other hand, increased the expression of FADD, a key adaptor molecule responsible for recruitment of caspase-8 to the Fas oligomer. The significance of the above changes was confirmed by the detection of considerably more caspase-8 in both the Fas or FADD immunoprecipitate obtained from cells treated with the doxorubicin/selenium combination.

Conclusion: Doxorubicin and selenium cooperatively activate Fas signaling by targeting key regulatory steps.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / pharmacology*
  • Apoptosis / drug effects
  • Breast Neoplasms / drug therapy
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology
  • Caspase 8 / metabolism
  • Cell Line, Tumor
  • Doxorubicin / administration & dosage
  • Doxorubicin / pharmacology*
  • Drug Synergism
  • Enzyme Activation
  • Fas Ligand Protein / metabolism*
  • Fas-Associated Death Domain Protein / metabolism
  • Humans
  • Immunoprecipitation
  • Organoselenium Compounds / administration & dosage
  • Organoselenium Compounds / pharmacology*
  • Receptors, Death Domain / metabolism
  • Signal Transduction / drug effects
  • TNF-Related Apoptosis-Inducing Ligand / metabolism
  • fas Receptor / metabolism*

Substances

  • FADD protein, human
  • Fas Ligand Protein
  • Fas-Associated Death Domain Protein
  • Organoselenium Compounds
  • Receptors, Death Domain
  • TNF-Related Apoptosis-Inducing Ligand
  • TNFSF10 protein, human
  • fas Receptor
  • Doxorubicin
  • methylselenic acid
  • Caspase 8