Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/119348
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Type: Journal article
Title: Extracellular fatty acids are the major contributor to lipid synthesis in prostate cancer
Author: Balaban, S.
Nassar, Z.
Zhang, A.
Hosseini-Beheshti, E.
Centenera, M.
Schreuder, M.
Lin, H.
Aishah, A.
Varney, B.
Liu-Fu, F.
Lee, L.
Nagarajan, S.
Shearer, R.
Hardie, R.
Raftopulos, N.
Kakani, M.
Saunders, D.
Holst, J.
Horvath, L.
Butler, L.
et al.
Citation: Molecular Cancer Research, 2019; 17(4):949-962
Publisher: American Association for Cancer Research
Issue Date: 2019
ISSN: 1541-7786
1557-3125
Statement of
Responsibility: 
Seher Balaban, Zeyad D. Nassar, Alison Y. Zhang, Elham Hosseini-Beheshti, Margaret M. Centenera, Mark Schreuder, Hui-Ming Lin, Atqiya Aishah, Bianca Varney, Frank Liu-Fu, Lisa S. Lee, Shilpa R. Nagarajan, Robert F. Shearer, Rae-Anne Hardie, Nikki L. Raftopulos, Meghna S. Kakani, Darren N. Saunders, Jeff Holst, Lisa G. Horvath, Lisa M. Butler, and Andrew J. Hoy
Abstract: Prostate cancer cells exhibit altered cellular metabolism but, notably, not the hallmarks of Warburg metabolism. Prostate cancer cells exhibit increased de novo synthesis of fatty acids (FA); however, little is known about how extracellular FAs, such as those in the circulation, may support prostate cancer progression. Here, we show that increasing FA availability increased intracellular triacylglycerol content in cultured patient-derived tumor explants, LNCaP and C4-2B spheroids, a range of prostate cancer cells (LNCaP, C4-2B, 22Rv1, PC-3), and prostate epithelial cells (PNT1). Extracellular FAs are the major source (∼83%) of carbons to the total lipid pool in all cell lines, compared with glucose (∼13%) and glutamine (∼4%), and FA oxidation rates are greater in prostate cancer cells compared with PNT1 cells, which preferentially partitioned extracellular FAs into triacylglycerols. Because of the higher rates of FA oxidation in C4-2B cells, cells remained viable when challenged by the addition of palmitate to culture media and inhibition of mitochondrial FA oxidation sensitized C4-2B cells to palmitate-induced apoptosis. Whereas in PC-3 cells, palmitate induced apoptosis, which was prevented by pretreatment of PC-3 cells with FAs, and this protective effect required DGAT-1-mediated triacylglycerol synthesis. These outcomes highlight for the first-time heterogeneity of lipid metabolism in prostate cancer cells and the potential influence that obesity-associated dyslipidemia or host circulating has on prostate cancer progression. IMPLICATIONS: Extracellular-derived FAs are primary building blocks for complex lipids and heterogeneity in FA metabolism exists in prostate cancer that can influence tumor cell behavior.
Keywords: Cell Line, Tumor; Extracellular Fluid; Humans; Prostatic Neoplasms; Lipids; Fatty Acids; Palmitates; Triglycerides; Male; Lipid Metabolism
Rights: ©2019 American Association for Cancer Research.
RMID: 0030107541
DOI: 10.1158/1541-7786.MCR-18-0347
Grant ID: http://purl.org/au-research/grants/arc/FT130101004
http://purl.org/au-research/grants/nhmrc/1052963
Appears in Collections:Medicine publications

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