Targeting Glutamine Addiction in Gliomas.
Marta Obara-MichlewskaMonika SzeligaPublished in: Cancers (2020)
The most common malignant brain tumors are those of astrocytic origin, gliomas, with the most aggressive glioblastoma (WHO grade IV) among them. Despite efforts, medicine has not made progress in terms of the prognosis and life expectancy of glioma patients. Behind the malignant phenotype of gliomas lies multiple genetic mutations leading to reprogramming of their metabolism, which gives those highly proliferating cells an advantage over healthy ones. The so-called glutamine addiction is a metabolic adaptation that supplements oxidative glycolysis in order to secure neoplastic cells with nutrients and energy in unfavorable conditions of hypoxia. The present review aims at presenting the research and clinical attempts targeting the different metabolic pathways involved in glutamine metabolism in gliomas. A brief description of the biochemistry of glutamine transport, synthesis, and glutaminolysis, etc. will forego a detailed comparison of the therapeutic strategies undertaken to inhibit glutamine utilization by gliomas.
Keyphrases
- high grade
- induced apoptosis
- cell cycle arrest
- end stage renal disease
- newly diagnosed
- ejection fraction
- cancer therapy
- prognostic factors
- endoplasmic reticulum stress
- peritoneal dialysis
- cell death
- gene expression
- oxidative stress
- endothelial cells
- quality improvement
- risk assessment
- copy number
- genome wide
- patient reported outcomes