학술논문

Glut3 Addiction Is a Druggable Vulnerability for a Molecularly Defined Subpopulation of Glioblastoma
Document Type
article
Source
Cancer Cell. 32(6)
Subject
Biochemistry and Cell Biology
Biomedical and Clinical Sciences
Biological Sciences
Brain Disorders
Stem Cell Research
Brain Cancer
Rare Diseases
Neurosciences
Stem Cell Research - Nonembryonic - Human
Cancer
Genetics
2.1 Biological and endogenous factors
Aetiology
Good Health and Well Being
Animals
Antineoplastic Agents
Brain Neoplasms
Cell Line
Tumor
Gene Expression Profiling
Glioblastoma
Glucose Transporter Type 3
Humans
Integrin alphaVbeta3
Kaplan-Meier Estimate
Mice
Mice
Nude
Signal Transduction
Snake Venoms
Transcriptome
Xenograft Model Antitumor Assays
Glut3
cancer stem cells
glioblastoma
glucose metabolism
integrin
Oncology and Carcinogenesis
Oncology & Carcinogenesis
Biochemistry and cell biology
Oncology and carcinogenesis
Language
Abstract
While molecular subtypes of glioblastoma (GBM) are defined using gene expression and mutation profiles, we identify a unique subpopulation based on addiction to the high-affinity glucose transporter, Glut3. Although Glut3 is a known driver of a cancer stem cell phenotype, direct targeting is complicated by its expression in neurons. Using established GBM lines and patient-derived stem cells, we identify a subset of tumors within the "proneural" and "classical" subtypes that are addicted to aberrant signaling from integrin αvβ3, which activates a PAK4-YAP/TAZ signaling axis to enhance Glut3 expression. This defined subpopulation of GBM is highly sensitive to agents that disrupt this pathway, including the integrin antagonist cilengitide, providing a targeted therapeutic strategy for this unique subset of GBM tumors.