Defining a Water-Soluble Formulation of Arachidonic Acid as a Novel Ferroptosis Inducer in Cancer Cells

被引:1
作者
Day, Zoe I. [1 ]
Mayfosh, Alyce J. [1 ,2 ]
Baxter, Amy A. [1 ]
Williams, Scott A. [1 ]
Hildebrand, Joanne M. [3 ]
Rau, Thomas F. [2 ]
Poon, Ivan K. H. [1 ]
Hulett, Mark D. [1 ]
机构
[1] La Trobe Univ, La Trobe Inst Mol Sci, Dept Biochem & Chem, Melbourne, Vic 3086, Australia
[2] Wintermute Biomed, Geelong, Vic 3220, Australia
[3] Walter & Eliza Hall Inst Med Res, Parkville, Vic 3052, Australia
关键词
ferroptosis; arachidonic acid; cell death; L-lysine; fatty acids; cancer; POLYUNSATURATED FATTY-ACIDS; MECHANISMS; PEROXIDATION; TRANSPORTER; INHIBITION; ROLES; DEATH; TNF;
D O I
10.3390/biom14050555
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Here, we describe GS-9, a novel water-soluble fatty acid-based formulation comprising L-lysine and arachidonic acid, that we have shown to induce ferroptosis. GS-9 forms vesicle-like structures in solution and mediates lipid peroxidation, as evidenced by increased C11-BODIPY fluorescence and an accumulation of toxic malondialdehyde, a downstream product of lipid peroxidation. Ferroptosis inhibitors counteracted GS-9-induced cell death, whereas caspase 3 and 7 or MLKL knock-out cell lines are resistant to GS-9-induced cell death, eliminating other cell death processes such as apoptosis and necroptosis as the mechanism of action of GS-9. We also demonstrate that through their role of sequestering fatty acids, lipid droplets play a protective role against GS-9-induced ferroptosis, as inhibition of lipid droplet biogenesis enhanced GS-9 cytotoxicity. In addition, Fatty Acid Transport Protein 2 was implicated in GS-9 uptake. Overall, this study identifies and characterises the mechanism of GS-9 as a ferroptosis inducer. This formulation of arachidonic acid offers a novel tool for investigating and manipulating ferroptosis in various cellular and anti-cancer contexts.
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页数:18
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