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Parkinson, E.K.* ; Adamski, J. ; Zahn, G.* ; Gaumann, A.* ; Flores-Borja, F.* ; Ziegler, C.* ; Mycielska, M.E.*

Extracellular citrate and metabolic adaptations of cancer cells.

Cancer Metastasis Rev., DOI: 10.1007/s10555-021-10007-1 (2021)
Verlagsversion DOI PMC
Open Access Hybrid
Creative Commons Lizenzvertrag
It is well established that cancer cells acquire energy via the Warburg effect and oxidative phosphorylation. Citrate is considered to play a crucial role in cancer metabolism by virtue of its production in the reverse Krebs cycle from glutamine. Here, we review the evidence that extracellular citrate is one of the key metabolites of the metabolic pathways present in cancer cells. We review the different mechanisms by which pathways involved in keeping redox balance respond to the need of intracellular citrate synthesis under different extracellular metabolic conditions. In this context, we further discuss the hypothesis that extracellular citrate plays a role in switching between oxidative phosphorylation and the Warburg effect while citrate uptake enhances metastatic activities and therapy resistance. We also present the possibility that organs rich in citrate such as the liver, brain and bones might form a perfect niche for the secondary tumour growth and improve survival of colonising cancer cells. Consistently, metabolic support provided by cancer-associated and senescent cells is also discussed. Finally, we highlight evidence on the role of citrate on immune cells and its potential to modulate the biological functions of pro- and anti-tumour immune cells in the tumour microenvironment. Collectively, we review intriguing evidence supporting the potential role of extracellular citrate in the regulation of the overall cancer metabolism and metastatic activity.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Review
Schlagwörter Cancer-associated Cells ; Citrate ; Oxphos ; Redox ; Senescence ; Warburg Effect; Pentose-phosphate Pathway; Malic Enzyme; Plasma Citrate; Oxidative Stress; Tumor Microenvironment; Lactate-dehydrogenase; Malate-dehydrogenase; Citric-acid; Dna-damage; Tca Cycle
Sprache englisch
Veröffentlichungsjahr 2021
HGF-Berichtsjahr 2021
ISSN (print) / ISBN 0167-7659
e-ISSN 1573-7233
Verlag Springer
Verlagsort Dordrecht, Netherlands
Begutachtungsstatus Peer reviewed
POF Topic(s) 30201 - Metabolic Health
Forschungsfeld(er) Genetics and Epidemiology
PSP-Element(e) G-500600-001
Förderungen Deutsche Forschungsgemeinschaft
Scopus ID 85121562488
PubMed ID 34932167
Erfassungsdatum 2022-01-11