Author:
Ainslie Anna P.,Klaver Myrthe,Voshart Daniëlle C.,Gerrits Emma,Eggen Bart J.L.,Bergink Steven,Barazzuol Lara
Abstract
AbstractProgressive neurocognitive dysfunction is the leading cause of a reduced quality of life in patients with primary brain tumours. Understanding the mechanisms underlying cognitive impairments that occur in response to a brain tumour and its treatment is essential to improve patients’ quality of life. Here, we show that normal-appearing non-tumour brain regions of patients with glioblastoma display hallmarks of accelerated ageing and share multiple features with Alzheimer’s disease patients. Integrated transcriptomic and tissue analysis shows that normal-appearing brain tissue from glioblastoma patients has a significant overlap with brain tissue from Alzheimer’s disease patients, revealing shared mitochondrial and neuronal dysfunction, and proteostasis deregulation. Overall, the brain of glioblastoma patients undergoes Alzheimer’s disease-like accelerated ageing, providing novel or repurposed therapeutic targets for managing brain cancer-related side effects.
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
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