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Targeting Glutamine Addiction in Gliomas

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...

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Autores principales: Obara-Michlewska, Marta, Szeliga, Monika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072559/
https://www.ncbi.nlm.nih.gov/pubmed/32013066
http://dx.doi.org/10.3390/cancers12020310
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author Obara-Michlewska, Marta
Szeliga, Monika
author_facet Obara-Michlewska, Marta
Szeliga, Monika
author_sort Obara-Michlewska, Marta
collection PubMed
description 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.
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spelling pubmed-70725592020-03-19 Targeting Glutamine Addiction in Gliomas Obara-Michlewska, Marta Szeliga, Monika Cancers (Basel) Review 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. MDPI 2020-01-29 /pmc/articles/PMC7072559/ /pubmed/32013066 http://dx.doi.org/10.3390/cancers12020310 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Obara-Michlewska, Marta
Szeliga, Monika
Targeting Glutamine Addiction in Gliomas
title Targeting Glutamine Addiction in Gliomas
title_full Targeting Glutamine Addiction in Gliomas
title_fullStr Targeting Glutamine Addiction in Gliomas
title_full_unstemmed Targeting Glutamine Addiction in Gliomas
title_short Targeting Glutamine Addiction in Gliomas
title_sort targeting glutamine addiction in gliomas
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072559/
https://www.ncbi.nlm.nih.gov/pubmed/32013066
http://dx.doi.org/10.3390/cancers12020310
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