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  Targeting Glutaminolysis: New Perspectives to Understand Cancer Development and Novel Strategies for Potential Target Therapies

Wang, Z., Liu, F., Fan, N., Zhou, C., Li, D., MacVicar, T., et al. (2020). Targeting Glutaminolysis: New Perspectives to Understand Cancer Development and Novel Strategies for Potential Target Therapies. Front Oncol, 10, 589508. doi:10.3389/fonc.2020.589508.

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externe Referenz:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7649373/ (beliebiger Volltext)
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 Urheber:
Wang, Z., Autor
Liu, F., Autor
Fan, N., Autor
Zhou, C., Autor
Li, D., Autor
MacVicar, T.1, Autor           
Dong, Q., Autor
Bruns, C. J., Autor
Zhao, Y., Autor
Affiliations:
1Department Langer - Mitochondrial Proteostasis, Max Planck Institute for Biology of Ageing, Max Planck Society, ou_3393994              

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Schlagwörter: cancer metabolism combination therapy glutaminase inhibitor glutaminolysis metastasis
 Zusammenfassung: Metabolism rewiring is an important hallmark of cancers. Being one of the most abundant free amino acids in the human blood, glutamine supports bioenergetics and biosynthesis, tumor growth, and the production of antioxidants through glutaminolysis in cancers. In glutamine dependent cancer cells, more than half of the tricarboxylic/critic acid (TCA) metabolites are derived from glutamine. Glutaminolysis controls the process of converting glutamine into TCA cycle metabolites through the regulation of multiple enzymes, among which the glutaminase shows the importance as the very first step in this process. Targeting glutaminolysis via glutaminase inhibition emerges as a promising strategy to disrupt cancer metabolism and tumor progression. Here, we review the regulation of glutaminase and the role of glutaminase in cancer metabolism and metastasis. Furthermore, we highlight the glutaminase inhibitor based metabolic therapy strategy and their potential applications in clinical scenarios.

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Sprache(n): eng - English
 Datum: 2020-10-262020-10-26
 Publikationsstatus: Erschienen
 Seiten: -
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: -
 Identifikatoren: Anderer: 33194749
DOI: 10.3389/fonc.2020.589508
ISSN: 2234-943X (Print)2234-943x
 Art des Abschluß: -

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Titel: Front Oncol
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: -
Seiten: - Band / Heft: 10 Artikelnummer: - Start- / Endseite: 589508 Identifikator: -