| Literature DB >> 33758075 |
Konstantin Drexler1, Katharina M Schmidt2, Katrin Jordan2, Marianne Federlin3, Vladimir M Milenkovic4, Gerhard Liebisch5, Anna Artati6, Christian Schmidl7, Gregor Madej8, Janina Tokarz6, Alexander Cecil6, Wolfgang Jagla9, Silke Haerteis10, Thiha Aung10,11, Christine Wagner2, Maria Kolodziejczyk2, Stefanie Heinke2, Evan H Stanton2, Barbara Schwertner1, Dania Riegel7, Christian H Wetzel4, Wolfgang Buchalla3, Martin Proescholdt12, Christoph A Klein13, Mark Berneburg1, Hans J Schlitt2, Thomas Brabletz14, Christine Ziegler8, Eric K Parkinson15, Andreas Gaumann9, Edward K Geissler2, Jerzy Adamski6,16,17, Sebastian Haferkamp18, Maria E Mycielska19.
Abstract
Citrate is important for lipid synthesis and epigenetic regulation in addition to ATP production. We have previously reported that cancer cells import extracellular citrate via the pmCiC transporter to support their metabolism. Here, we show for the first time that citrate is supplied to cancer by cancer-associated stroma (CAS) and also that citrate synthesis and release is one of the latter's major metabolic tasks. Citrate release from CAS is controlled by cancer cells through cross-cellular communication. The availability of citrate from CAS regulated the cytokine profile, metabolism and features of cellular invasion. Moreover, citrate released by CAS is involved in inducing cancer progression especially enhancing invasiveness and organ colonisation. In line with the in vitro observations, we show that depriving cancer cells of citrate using gluconate, a specific inhibitor of pmCiC, significantly reduced the growth and metastatic spread of human pancreatic cancer cells in vivo and muted stromal activation and angiogenesis. We conclude that citrate is supplied to tumour cells by CAS and citrate uptake plays a significant role in cancer metastatic progression.Entities:
Year: 2021 PMID: 33758075 PMCID: PMC7994318 DOI: 10.26508/lsa.202000903
Source DB: PubMed Journal: Life Sci Alliance ISSN: 2575-1077