Abstract
TRAIL is a promising therapeutic agent for human malignancies. TRAIL often requires mitochondrial dysfunction, referred to as the Type II death receptor pathway, to promote cytotoxicity. However, numerous malignant cells are TRAIL resistant due to inhibition of this mitochondrial pathway. Using cholangiocarcinoma cells as a model of TRAIL resistance, we found that Hedgehog signaling blockade sensitized these cancer cells to TRAIL cytotoxicity independent of mitochondrial dysfunction, referred to as Type I death receptor signaling. This switch in TRAIL requirement from Type II to Type I death receptor signaling was demonstrated by the lack of functional dependence on Bid/Bim and Bax/Bak, proapoptotic components of the mitochondrial pathway. Hedgehog signaling modulated expression of X-linked inhibitor of apoptosis (XIAP), which serves to repress the Type I death receptor pathway. siRNA targeted knockdown of XIAP mimics sensitization to mitochondria-independent TRAIL killing achieved by Hedgehog inhibition. Regulation of XIAP expression by Hedgehog signaling is mediated by the glioma-associated oncogene 2 (GLI2), a downstream transcription factor of Hedgehog. In conclusion, these data provide additional mechanisms modulating cell death by TRAIL and suggest Hedgehog inhibition as a therapeutic approach for TRAIL-resistant neoplasms.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Apoptosis / drug effects
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Apoptosis Regulatory Proteins / genetics
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Apoptosis Regulatory Proteins / metabolism
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BH3 Interacting Domain Death Agonist Protein / genetics
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BH3 Interacting Domain Death Agonist Protein / metabolism
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Bcl-2-Like Protein 11
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Cell Line
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Cell Line, Tumor
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Chromatin Immunoprecipitation
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Electrophoretic Mobility Shift Assay
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Hedgehog Proteins / genetics
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Hedgehog Proteins / metabolism*
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Humans
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Immunoblotting
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Inhibitor of Apoptosis Proteins / genetics
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Inhibitor of Apoptosis Proteins / metabolism
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Kruppel-Like Transcription Factors / genetics
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Kruppel-Like Transcription Factors / metabolism
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Membrane Proteins / genetics
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Membrane Proteins / metabolism
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Nuclear Proteins / genetics
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Nuclear Proteins / metabolism
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Promoter Regions, Genetic / genetics
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Proto-Oncogene Proteins / genetics
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Proto-Oncogene Proteins / metabolism
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RNA Interference
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Reverse Transcriptase Polymerase Chain Reaction
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Signal Transduction / drug effects
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Signal Transduction / genetics
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TNF-Related Apoptosis-Inducing Ligand / pharmacology
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Transcription Factors / genetics
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Transcription Factors / metabolism
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Veratrum Alkaloids / pharmacology
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X-Linked Inhibitor of Apoptosis Protein / genetics
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X-Linked Inhibitor of Apoptosis Protein / metabolism
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Zinc Finger Protein GLI1
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Zinc Finger Protein Gli2
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bcl-2 Homologous Antagonist-Killer Protein / genetics
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bcl-2 Homologous Antagonist-Killer Protein / metabolism
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bcl-2-Associated X Protein / genetics
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bcl-2-Associated X Protein / metabolism
Substances
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Apoptosis Regulatory Proteins
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BCL2L11 protein, human
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BH3 Interacting Domain Death Agonist Protein
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BID protein, human
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Bcl-2-Like Protein 11
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GLI1 protein, human
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GLI2 protein, human
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Hedgehog Proteins
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Inhibitor of Apoptosis Proteins
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Kruppel-Like Transcription Factors
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Membrane Proteins
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Nuclear Proteins
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Proto-Oncogene Proteins
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TNF-Related Apoptosis-Inducing Ligand
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Transcription Factors
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Veratrum Alkaloids
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X-Linked Inhibitor of Apoptosis Protein
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XIAP protein, human
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Zinc Finger Protein GLI1
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Zinc Finger Protein Gli2
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bcl-2 Homologous Antagonist-Killer Protein
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bcl-2-Associated X Protein
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cyclopamine