Rescue of cognitive function following fractionated brain irradiation in a novel preclinical glioma model.
Xi FengSharon LiuDavid ChenSusanna RosiNalin GuptaPublished in: eLife (2018)
More than half of long-term brain tumor survivors develop irreversible cognitive decline that severely affect their quality of life. However, there is no pre-clinical model that allows long-term assessment of cognition, and there is no treatment which ameliorates cognitive deficits in patients. Here, we report a novel glioma mouse model that offers manageable tumor growth and reliable assessment of cognitive functions in a post-treatment manner. Using this model, we found that fractionated whole-brain irradiation (fWBI), but not tumor growth, results in memory deficits. Transient inhibition of CSF-1R during fWBI prolongs survival of glioma-bearing mice and fully prevents fWBI-induced memory deficits. This result suggests that CSF-1R inhibition during radiotherapy can be explored as an approach to improve both survival and cognitive outcomes in patients who will receive fWBI. Taken together, the current study provides a proof of concept of a powerful tool to study radiation-induced cognitive deficits in glioma-bearing animals.
Keyphrases
- radiation induced
- cognitive decline
- mouse model
- radiation therapy
- mild cognitive impairment
- white matter
- traumatic brain injury
- end stage renal disease
- resting state
- cerebral ischemia
- chronic kidney disease
- mesenchymal stem cells
- newly diagnosed
- ejection fraction
- early stage
- stem cells
- prognostic factors
- squamous cell carcinoma
- metabolic syndrome
- type diabetes
- weight loss
- adipose tissue
- oxidative stress
- high glucose
- insulin resistance
- functional connectivity
- bone marrow
- brain metastases
- stress induced
- subarachnoid hemorrhage
- high fat diet induced
- clinical evaluation