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MET kinase fusions in pediatric glioblastoma

儿童胶质母细胞瘤中的 MET 激酶融合

基本信息

批准号：
10373782
负责人：
Renee D Read
金额：
$ 23.48万
依托单位：
EMORY UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2021
资助国家：
美国
起止时间：
2021-12-01 至 2023-11-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/10373782
关键词：
Adhesions Adopted Adult Apoptosis Astrocytes Automobile Driving Biological Process Blocking Antibodies Blood - brain barrier anatomy Brain Brain Diseases C-terminal Cancer Etiology Cells Child Childhood Childhood Glioblastoma Childhood Glioma Clinical Research Clinical Trials Clustered Regularly Interspaced Short Palindromic Repeats Cytokine Signaling Cytoplasmic Protein Data Development Doctor of Philosophy Drug Tolerance Drug resistance Experimental Models FDA approved Genetic Glioma Goals Growth IRAK4 gene Immune Immunocompetent Immunosuppression In Vitro Inflammation Inflammatory Interferon Receptor Interferons Investigation Lead Lesion Malignant - descriptor Mediating Modeling Mutation N-terminal Natural Immunity Neoplasm Metastasis Oncogenic Pathway interactions Patients Pediatric Neoplasm Pharmaceutical Preparations Pharmacology Phosphotransferases Precision therapeutics Primary Brain Neoplasms Process Protein Tyrosine Kinase Proteins Proteomics Publishing RNA Interference Receptor Protein-Tyrosine Kinases Research Resistance Resistance development STAT1 gene Signal Pathway Signal Transduction TBK1 gene TLR4 gene TP53 gene Testing Therapeutic Agents Tissues Toll-like receptors Treatment Efficacy Tumor Stem Cells Tumor Suppressor Proteins Tumor-Derived Tyrosine Kinase Inhibitor Variant Xenograft procedure antitumor effect autocrine base brain tissue cell type chemokine childhood cancer mortality cytokine differential expression effective therapy experimental study extracellular genetic approach human model improved in vivo insight kinase inhibitor migration mouse model mutant neoplastic cell nerve stem cell new therapeutic target novel therapeutics overexpression paracrine precision medicine predicting response predictive marker prevent programs protein protein interaction receptor recruit relating to nervous system resistance mechanism response small molecule stem stem cell function stem cell model stem cells stem-like cell synergism therapeutic evaluation therapeutic target therapy design transcriptomics treatment strategy tumor tumor microenvironment tumor progression tumorigenesis

项目摘要

ABSTRACT High grade gliomas (HGGs), the most deadly malignant primary brain tumors in children, and are incurable with current therapies. To find mutations that drive formation and progression of pediatric HGGs (pHGGs), we genomically characterized over 25 tumors, and we identified fusion mutations in the MET and ALK receptor tyrosine kinases. Recent comprehensive analyses show that RTK fusions are found in up to 40% of pHGGs, and among the most common are MET and ALK fusions, found in more than 10% of pHGGs. Our and others’ data show that for many RTK fusions, in which the C-terminal kinase domain is fused to N-terminal regions of other proteins that are normally highly expressed in neuro-glial stem/progenitor cells, indicating that MET fusions are likely overexpressed as a consequence of developmental programs. Our results show that RTK fusions, such as the MET fusions, create constitutively active kinases capable of transforming neural stem cells into pHGG-like tumors. FDA-approved small molecule tyrosine kinase inhibitors (TKIs) exist that penetrate the blood-brain barrier that may benefit pHGG patients with MET and ALK fusions as well as other RTK fusions, and these TKIs are being tested in patients with RTK fusions on an investigational basis. However, despite initial responses, MET fusion pHGG patients quickly developed resistant secondary tumors. Therefore, we are using our experiments MET fusion models, which include patient-derived pHGG tumor stem cells and xenografts as well as immunocompetent pHGG mouse models, to discover TKI resistance mechanisms. Already, our preliminary studies implicate cell-intrinsic innate immunity and inflammatory cytokine signaling in TKI drug tolerance and emergence of resistance among pHGG cells with MET fusions. To discover and study resistance mechanisms for MET and other RTK fusions in pHGG, we propose to two aims to 1) examine interactions between RTK fusions, RTK kinase inhibitors, and inflammatory cytokine signaling pathways and their effectors in vitro and in vivo in the brain using our robust MET fusion models, and to 2) test synergy between RTK kinase inhibitors and inflammatory pathway inhibition using pharmacologic and genetic approaches. We will use additional models of RTK fusions pHGGs to determine if our observations are generalizable among pHGGs with RTK fusions. The results of our research may lead to development of new combination precision treatment strategies for pHGG.

摘要