Ontology highlight
ABSTRACT: Background
Glioblastoma (GBM) is an aggressive, age-associated malignant glioma that contains populations of cancer stem cells. These glioma stem cells (GSCs) evade therapeutic interventions and repopulate tumors due to their existence in a slowly cycling quiescent state. Although aging is well known to increase cancer initiation, the extent to which the mechanisms supporting GSC tumorigenicity are related to physiological aging remains unknown.Aims
Here, we investigate the transcriptional mechanisms by which Forkhead Box O3 (FOXO3), a transcriptional regulator that promotes healthy aging, affects GSC function and the extent to which FOXO3 transcriptional networks are dysregulated in aging and GBM.Methods and results
We performed transcriptome analysis of clinical G
SUBMITTER: Audesse AJ
PROVIDER: S-EPMC9601604 | biostudies-literature | 2021 Dec
REPOSITORIES: biostudies-literature