c-FLIP knockdown induces ligand-independent DR5-, FADD-, caspase-8-, and caspase-9-dependent apoptosis in breast cancer cells

Travis W. Day, Su Huang, Ahmad R. Safa

Research output: Contribution to journalArticle

62 Scopus citations

Abstract

Cellular-FLICE inhibitory protein (c-FLIP) is an inhibitor of apoptosis downstream of the death receptors Fas, DR4, and DR5, and is expressed as long (c-FLIPL) and short (c-FLIPS) splice forms. We found that the knockdown of c-FLIP using small interfering RNA (siRNA) triggered ligand-independent caspase-8- and -9-dependent spontaneous apoptosis and decreased the proliferation of MCF-7 breast cancer cells. Further analysis revealed that an apoptotic inhibitory complex (AIC) comprised of DR5, FADD, caspase-8, and c-FLIPL exists in MCF-7 cells, and the absence of c-FLIPL from this complex induces DR5- and FADD-mediated caspase-8 activation in the death inducing signaling complex (DISC). c-FLIPS was not detected in the AIC, and using splice form-specific siRNAs we showed that c-FLIPL but not c-FLIPS is required to prevent spontaneous death signaling in MCF-7 cells. These results clearly show that c-FLIPL prevents ligand-independent death signaling and provides direct support for studying c-FLIP as a relevant therapeutic target for breast cancers.

Original languageEnglish (US)
Pages (from-to)1694-1704
Number of pages11
JournalBiochemical Pharmacology
Volume76
Issue number12
DOIs
StatePublished - Dec 15 2008

Keywords

  • Apoptosis
  • Breast cancer
  • c-FLIP
  • Small interfering RNA (siRNA)
  • TRAIL receptor 5

ASJC Scopus subject areas

  • Pharmacology
  • Biochemistry

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