Molecular Oncology · 2024 · 12 citations · 45 references
MedicineMolecular BiologyOncologyEpigeneticsMolecular OncologyTumor ProgressionCancer GenomicsCancer Stem Cell BiologyCancer Stem CellsEpigenetic Regulation In CancerNoncoding Rna BiologyNoncoding Rna FunctionCancer Stem Cell-mediated ResistanceGlioblastoma EpigeneticsGlioblastoma Stem CellsNeuronal Lineage SpecificationPrimary Brain NeoplasmsStem Cell Fate SpecificationStem Cell SpecificationTherapy-resistant Cancer Stem Cells
Glioblastoma is the most common primary malignant brain tumor in adults, with a median survival of just over 1 year. The failure of available treatments to achieve remission in patients with glioblastoma (GBM) has been attributed to the presence of cancer stem cells (CSCs), which are thought to play a central role in tumor development and progression and serve as a treatment-resistant cell repository capable of driving tumor recurrence. In fact, the property of "stemness" itself may be responsible for treatment resistance. In this study, we identify a novel long noncoding RNA (lncRNA), cancer stem cell-associated distal enhancer of SOX2 (CASCADES), that functions as an epigenetic regulator in glioma CSCs (GSCs). CASCADES is expressed in isocitrate dehydrogenase (IDH)-wild-type GBM and is significantly enriched in GSCs. Knockdown of CASCADES in GSCs results in differentiation towards a neuronal lineage in a cell- and cancer-specific manner. Bioinformatics analysis reveals that CASCADES functions as a super-enhancer-associated lncRNA epigenetic regulator of SOX2. Our findings identify CASCADES as a critical regulator of stemness in GSCs that represents a novel epigenetic and therapeutic target for disrupting the CSC compartment in glioblastoma.
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Radiotherapy plus Concomitant and Adjuvant Temozolomide for Glioblastoma
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