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Restoration of TRAIL-induced apoptosis in resistant human pancreatic cancer cells by a novel FAK inhibitor, PH11

Authors :
Pascal Dao
Nikaïa Smith
Daniel Scott-Algara
Christiane Garbay
Huixiong Chen
Jean-Philippe Herbeuval
Laboratoire de Chimie et de Biochimie Pharmacologiques et Toxicologiques (LCBPT - UMR 8601)
Université Paris Descartes - Paris 5 (UPD5)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
Régulation des Infections Rétrovirales
Institut Pasteur [Paris]
Institut Pasteur [Paris] (IP)
Source :
Cancer Letters, Cancer Letters, Elsevier, 2015, 360 (1), pp.48-59. ⟨10.1016/j.canlet.2015.02.016⟩, Cancer Letters, 2015, 360 (1), pp.48-59. ⟨10.1016/j.canlet.2015.02.016⟩
Publication Year :
2015
Publisher :
HAL CCSD, 2015.

Abstract

International audience; Tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) emerges as one of the most-promising experimental cancer therapeutic drugs and is currently being tested in clinical trials. However, both intrinsic and acquired resistance of human cancer cells to TRAIL-induced apoptosis poses a huge problem in establishing clinically efficient TRAIL therapies. To assess the regulation of TRAIL-resistance in human pancreatic cancer cells, we studied the TRAIL resistant pancreatic cell line PANC-1. We show that treatment with PH11, a novel Focal Adhesion Kinase (FAK) inhibitor in association with TRAIL rapidly induces apoptosis in TRAIL-resistant PANC-1 cells, but not in normal human fibroblast cells. To explain sensitization, we showed that PH11 restores TRAIL apoptotic pathway in PANC-1 cells through down-regulation of c-FLIP via inhibition of FAK and the phosphatidylinositol-3 kinase (PI3K)/AKT pathways. These findings suggest that this combined treatment may offer an attractive therapeutic strategy for safely and efficiently treating pancreatic cancer.

Subjects

Subjects :
MESH: Signal Transduction
Cancer Research
MESH: CASP8 and FADD-Like Apoptosis Regulating Protein
Time Factors
MESH: Triazines
CASP8 and FADD-Like Apoptosis Regulating Protein
Apoptosis
TRAIL
FAK inhibitor
[SDV.IMM.II]Life Sciences [q-bio]/Immunology/Innate immunity
MESH: Dose-Response Relationship, Drug
TNF-Related Apoptosis-Inducing Ligand
0302 clinical medicine
MESH: Molecular Targeted Therapy
Medicine
MESH: Protein Kinase Inhibitors
Molecular Targeted Therapy
0303 health sciences
Kinase
Triazines
Imidazoles
MESH: Drug Resistance, Neoplasm
3. Good health
Cell biology
Oncology
030220 oncology & carcinogenesis
Caspases
[SDV.IMM]Life Sciences [q-bio]/Immunology
Tumor necrosis factor alpha
RNA Interference
MESH: Pancreatic Neoplasms
MESH: TNF-Related Apoptosis-Inducing Ligand
MESH: Imidazoles
Signal Transduction
MESH: Focal Adhesion Kinase 1
MESH: Enzyme Activation
c-FLIP
MESH: Cell Line, Tumor
MESH: RNA Interference
Antineoplastic Agents
Transfection
Focal adhesion
03 medical and health sciences
Pancreatic cancer
Cell Line, Tumor
Humans
Protein kinase B
Protein Kinase Inhibitors
PI3K/AKT/mTOR pathway
030304 developmental biology
Pancreatic cancer cell lines
MESH: Caspases
MESH: Humans
Dose-Response Relationship, Drug
business.industry
MESH: Proto-Oncogene Proteins c-akt
MESH: Apoptosis
MESH: Transfection
MESH: Time Factors
Cancer
medicine.disease
Enzyme Activation
Pancreatic Neoplasms
PI3K/AKT pathway
Drug Resistance, Neoplasm
Focal Adhesion Kinase 1
Cancer research
MESH: Antineoplastic Agents
MESH: Phosphatidylinositol 3-Kinase
Phosphatidylinositol 3-Kinase
business
Proto-Oncogene Proteins c-akt

Details

Language :
English
ISSN :
03043835
Database :
OpenAIRE
Journal :
Cancer Letters, Cancer Letters, Elsevier, 2015, 360 (1), pp.48-59. ⟨10.1016/j.canlet.2015.02.016⟩, Cancer Letters, 2015, 360 (1), pp.48-59. ⟨10.1016/j.canlet.2015.02.016⟩
Accession number :
edsair.doi.dedup.....aff89ae0cba6df104e704d11ff6b16fd