Radiation-Induced Cellular Plasticity: A Strategy for Combatting Glioblastoma.
Ling HeDaria AzizadKruttika BhatAngeliki IoannidisCarter J HoffmannEvelyn ArambulaAparna BhaduriHarley I KornblumFrank PajonkPublished in: bioRxiv : the preprint server for biology (2024)
Glioblastoma is the deadliest brain cancer in adults and almost all patients succumb to the tumor. While surgery followed by chemo-radiotherapy significantly delays disease progression, these treatments do not lead to long-term tumor control and targeted therapies or biologics have so far failed to further improve survival. Utilizing a transient radiation-induced state of multipotency we used the adenylcyclase activator forskolin to alter the cellular fate of glioma cells in response to radiation. The combined treatment induced the expression of neuronal markers in glioma cells, reduced proliferation and led to a distinct gene expression profile. scRNAseq revealed that the combined treatment forced glioma cells into a microglia- and neuron-like phenotypes. In vivo this treatment led to a loss of glioma stem cells and prolonged median survival in mouse models of glioblastoma. Collectively, our data suggest that revisiting a differentiation therapy with forskolin in combination with radiation could lead to clinical benefit.
Keyphrases
- radiation induced
- stem cells
- radiation therapy
- poor prognosis
- early stage
- end stage renal disease
- mouse model
- combination therapy
- immune response
- photodynamic therapy
- squamous cell carcinoma
- chronic kidney disease
- inflammatory response
- single cell
- spinal cord
- machine learning
- white matter
- rectal cancer
- coronary artery disease
- mesenchymal stem cells
- bone marrow
- ejection fraction
- replacement therapy
- drug induced
- spinal cord injury
- blood brain barrier
- neuropathic pain
- oxidative stress
- smoking cessation
- genome wide
- young adults
- electronic health record
- lymph node metastasis