Targeting c-FLIP in cancer

Cancer Lett. 2013 May 28;332(2):141-50. doi: 10.1016/j.canlet.2010.10.009. Epub 2010 Nov 10.

Abstract

Cellular-FLICE inhibitory protein (c-FLIP) is a key anti-apoptotic regulator that inhibits cell death mediated by the death receptors Fas, DR4, DR5, and TNF-R1. Three splice variants of c-FLIP function at the DISC level by blocking the processing and activation of procaspase-8 and -10. Overexpression of c-FLIP has been identified in many different tumour types, and its downregulation in vitro has been shown to restore apoptosis mediated by CD95L and TRAIL. c-FLIP therefore represents a promising target for cancer therapy. This review focuses on the molecular mechanisms that control c-FLIP expression and current research into inhibitors of the protein. Increasing evidence supports the investigation of c-FLIP as a therapeutic target to restore an apoptotic response in cancer cells.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Apoptosis*
  • CASP8 and FADD-Like Apoptosis Regulating Protein / metabolism*
  • Fas Ligand Protein / metabolism
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Ligands
  • Neoplasms / drug therapy*
  • Neoplasms / metabolism*
  • Neoplasms / pathology
  • Protein Processing, Post-Translational
  • RNA, Small Interfering / metabolism
  • TNF-Related Apoptosis-Inducing Ligand / metabolism
  • Transcription, Genetic

Substances

  • Antineoplastic Agents
  • CASP8 and FADD-Like Apoptosis Regulating Protein
  • CFLAR protein, human
  • Fas Ligand Protein
  • Ligands
  • RNA, Small Interfering
  • TNF-Related Apoptosis-Inducing Ligand