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

Author:

Day Zoe I.1ORCID,Mayfosh Alyce J.12ORCID,Baxter Amy A.1,Williams Scott A.1,Hildebrand Joanne M.3ORCID,Rau Thomas F.2,Poon Ivan K. H.1,Hulett Mark D.1ORCID

Affiliation:

1. Department of Biochemistry and Chemistry, La Trobe Institute for Molecular Science, La Trobe University, Melbourne, VIC 3086, Australia

2. Wintermute Biomedical, Geelong, VIC 3220, Australia

3. The Walter and Eliza Hall Institute of Medical Research, Parkville, VIC 3052, Australia

Abstract

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.

Funder

Cooperative Research Centre project (CRC-P) grant from AusIndustry, Department of Industry, Science, Energy and Resources

Publisher

MDPI AG

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