Elevated Asparagine Biosynthesis Drives Brain Tumor Stem Cell Metabolic Plasticity and Resistance to Oxidative Stress.
Tom M ThomasKen MiyaguchiLincoln A EdwardsHongqiang WangHassen WolleboLi AiguoRamachandran MuraliYizhou WangDaniel BraasJustin S MichaelAllen M AndresMiqin ZhangKamel KhaliliRoberta A GottliebJ Manuel PerezJohn S YuPublished in: Molecular cancer research : MCR (2021)
Asparagine synthetase (ASNS) is a gene on the long arm of chromosome 7 that is copy-number amplified in the majority of glioblastomas. ASNS copy-number amplification is associated with a significantly decreased survival. Using patient-derived glioma stem cells (GSC), we showed that significant metabolic alterations occur in gliomas when perturbing the expression of ASNS, which is not merely restricted to amino acid homeostasis. ASNS-high GSCs maintained a slower basal metabolic profile yet readily shifted to a greatly increased capacity for glycolysis and oxidative phosphorylation when needed. This led ASNS-high cells to a greater ability to proliferate and spread into brain tissue. Finally, we demonstrate that these changes confer resistance to cellular stress, notably oxidative stress, through adaptive redox homeostasis that led to radiotherapy resistance. Furthermore, ASNS overexpression led to modifications of the one-carbon metabolism to promote a more antioxidant tumor environment revealing a metabolic vulnerability that may be therapeutically exploited. IMPLICATIONS: This study reveals a new role for ASNS in metabolic control and redox homeostasis in glioma stem cells and proposes a new treatment strategy that attempts to exploit one vulnerable metabolic node within the larger multilayered tumor network.
Keyphrases
- copy number
- stem cells
- mitochondrial dna
- oxidative stress
- genome wide
- induced apoptosis
- amino acid
- dna methylation
- transcription factor
- dna damage
- cell therapy
- heat shock
- climate change
- white matter
- radiation therapy
- anti inflammatory
- mesenchymal stem cells
- high grade
- brain injury
- gene expression
- locally advanced
- cell death
- combination therapy
- radiation induced
- long non coding rna
- functional connectivity
- heat stress
- cell cycle arrest