Ontology highlight
ABSTRACT: Background
Glioblastoma is the most common malignant brain tumor in adults. Cellular plasticity and the poorly differentiated features result in a fast relapse of the tumors following treatment. Moreover, the immunosuppressive microenvironment proved to be a major obstacle to immunotherapeutic approaches. Branched-chain amino acid transaminase 1 (BCAT1) was shown to drive the growth of glioblastoma and other cancers;however, its oncogenic mechanism remains poorly understood.Methods
Using human tumor data, cell line models and orthotopic immuno-competent and -deficient mouse models, we investigated the phenotypic and mechanistic effects of BCAT1 on glioblastoma cell state and immunomodulation.Results
Here, we show that BCAT1 is crucial for maintaining the poorly diff
SUBMITTER: Boskovic P
PROVIDER: S-EPMC10836774 | biostudies-literature | 2024 Feb
REPOSITORIES: biostudies-literature