Your browser doesn't support javascript.
loading
Kinome Profiling of NF1-Related MPNSTs in Response to Kinase Inhibition and Doxorubicin Reveals Therapeutic Vulnerabilities.
Grit, Jamie L; Pridgeon, Matt G; Essenburg, Curt J; Wolfrum, Emily; Madaj, Zachary B; Turner, Lisa; Wulfkuhle, Julia; Petricoin, Emanuel F; Graveel, Carrie R; Steensma, Matthew R.
Affiliation
  • Grit JL; Center for Cancer and Cell Biology, Van Andel Research Institute, Grand Rapids, MI 49503, USA.
  • Pridgeon MG; Center for Cancer and Cell Biology, Van Andel Research Institute, Grand Rapids, MI 49503, USA.
  • Essenburg CJ; Helen DeVos Children's Hospital, Spectrum Health System, Grand Rapids, MI 49503, USA.
  • Wolfrum E; Center for Cancer and Cell Biology, Van Andel Research Institute, Grand Rapids, MI 49503, USA.
  • Madaj ZB; Bioinformatics & Biostatistics Core, Van Andel Research Institute, Grand Rapids, MI 49503, USA.
  • Turner L; Bioinformatics & Biostatistics Core, Van Andel Research Institute, Grand Rapids, MI 49503, USA.
  • Wulfkuhle J; Pathology and Biorepository Core, Van Andel Research Institute, Grand Rapids, MI 49503, USA.
  • Petricoin EF; Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA 22030, USA.
  • Graveel CR; Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA 22030, USA.
  • Steensma MR; Center for Cancer and Cell Biology, Van Andel Research Institute, Grand Rapids, MI 49503, USA.
Genes (Basel) ; 11(3)2020 03 20.
Article in En | MEDLINE | ID: mdl-32245042
Neurofibromatosis Type 1 (NF1)-related Malignant Peripheral Nerve Sheath Tumors (MPNST) are highly resistant sarcomas that account for significant mortality. The mechanisms of therapy resistance are not well-understood in MPNSTs, particularly with respect to kinase inhibition strategies. In this study, we aimed to quantify the impact of both the genomic context and targeted therapy on MPNST resistance using reverse phase phosphoproteome array (RPPA) analysis. We treated tumorgrafts from three genetically engineered mouse models using MET (capmatinib) and MEK (trametinib) inhibitors and doxorubicin, and assessed phosphosignaling at 4 h, 2 days, and 21 days. Baseline kinase signaling in our mouse models recapitulated an MET-addicted state (NF1-MET), P53 mutation (NF1-P53), and HGF overexpression (NF1). Following perturbation with the drug, we observed broad and redundant kinome adaptations that extended well beyond canonical RAS/ERK or PI3K/AKT/mTOR signaling. MET and MEK inhibition were both associated with an initial inflammatory response mediated by kinases in the JAK/STAT pathway and NFkB. Growth signaling predominated at the 2-day and 21-day time points as a result of broad RTK and intracellular kinase activation. Interestingly, AXL and NFkB were strongly activated at the 2-day and 21-day time points, and tightly correlated, regardless of the treatment type or genomic context. The degree of kinome adaptation observed in innately resistant tumors was significantly less than the surviving fractions of responsive tumors that exhibited a latency period before reinitiating growth. Lastly, doxorubicin resistance was associated with kinome adaptations that strongly favored growth and survival signaling. These observations confirm that MPNSTs are capable of profound signaling plasticity in the face of kinase inhibition or DNA damaging agent administration. It is possible that by targeting AXL or NFkB, therapy resistance can be mitigated.
Subject(s)
Antineoplastic Agents/therapeutic use; MAP Kinase Signaling System; Nerve Sheath Neoplasms/drug therapy; Protein Kinase Inhibitors/pharmacology; Proteome/metabolism; Animals; Antineoplastic Agents/administration & dosage; Antineoplastic Combined Chemotherapy Protocols; Benzamides; Doxorubicin/administration & dosage; Doxorubicin/therapeutic use; Extracellular Signal-Regulated MAP Kinases/antagonists & inhibitors; Extracellular Signal-Regulated MAP Kinases/genetics; Extracellular Signal-Regulated MAP Kinases/metabolism; Imidazoles/administration & dosage; Imidazoles/therapeutic use; Mice; Mice, SCID; NF-kappa B/genetics; NF-kappa B/metabolism; Nerve Sheath Neoplasms/genetics; Neurofibromin 1/genetics; Phosphatidylinositol 3-Kinases/genetics; Phosphatidylinositol 3-Kinases/metabolism; Protein Kinase Inhibitors/administration & dosage; Protein Kinase Inhibitors/therapeutic use; Proteome/genetics; Proto-Oncogene Proteins c-akt/antagonists & inhibitors; Proto-Oncogene Proteins c-akt/genetics; Proto-Oncogene Proteins c-akt/metabolism; Pyridones/administration & dosage; Pyridones/therapeutic use; Pyrimidinones/administration & dosage; Pyrimidinones/therapeutic use; STAT Transcription Factors/genetics; STAT Transcription Factors/metabolism; TOR Serine-Threonine Kinases/genetics; TOR Serine-Threonine Kinases/metabolism; Topoisomerase II Inhibitors/administration & dosage; Topoisomerase II Inhibitors/therapeutic use; Triazines/administration & dosage; Triazines/therapeutic use; ras Proteins/genetics; ras Proteins/metabolism
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Nerve Sheath Neoplasms / MAP Kinase Signaling System / Proteome / Protein Kinase Inhibitors / Antineoplastic Agents Type of study: Prognostic_studies Language: En Journal: Genes (Basel) Year: 2020 Document type: Article Affiliation country: United States Country of publication: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Nerve Sheath Neoplasms / MAP Kinase Signaling System / Proteome / Protein Kinase Inhibitors / Antineoplastic Agents Type of study: Prognostic_studies Language: En Journal: Genes (Basel) Year: 2020 Document type: Article Affiliation country: United States Country of publication: Switzerland