|Title||Targeted reduction of cholesterol uptake in cholesterol-addicted lymphoma cells blocks turnover of oxidized lipids to cause ferroptosis.|
|Publication Type||Journal Article|
|Year of Publication||2021|
|Authors||Rink JS, Lin AYuh, McMahon KM, Calvert AE, Yang S, Taxter T, Moreira J, Chadburn A, Behdad A, Karmali R, C Thaxton S, Gordon LI|
|Journal||J Biol Chem|
|Date Published||2021 Jan-Jun|
|Keywords||Animals, Cholesterol, Ferroptosis, Humans, Jurkat Cells, Lymphoma, Mice, Mice, SCID, Neoplasm Proteins, Oxidation-Reduction, Phospholipid Hydroperoxide Glutathione Peroxidase, Scavenger Receptors, Class B, U937 Cells|
Normal human cells can either synthesize cholesterol or take it up from lipoproteins to meet their metabolic requirements. In some malignant cells, de novo cholesterol synthesis genes are transcriptionally silent or mutated, meaning that cholesterol uptake from lipoproteins is required for survival. Recent data suggest that lymphoma cells dependent upon lipoprotein-mediated cholesterol uptake are also subject to ferroptosis, an oxygen- and iron-dependent cell death mechanism triggered by accumulation of oxidized lipids in cell membranes unless the lipid hydroperoxidase, glutathione peroxidase 4 (GPX4), reduces these toxic lipid species. To study mechanisms linking cholesterol uptake with ferroptosis and determine the potential role of the high-density lipoprotein (HDL) receptor as a target for cholesterol depleting therapy, we treated lymphoma cell lines known to be sensitive to the reduction of cholesterol uptake with HDL-like nanoparticles (HDL NPs). HDL NPs are a cholesterol-poor ligand that binds to the receptor for cholesterol-rich HDLs, scavenger receptor type B1 (SCARB1). Our data reveal that HDL NP treatment activates a compensatory metabolic response in treated cells toward increased de novo cholesterol synthesis, which is accompanied by nearly complete reduction in expression of GPX4. As a result, oxidized membrane lipids accumulate, leading to cell death through a mechanism consistent with ferroptosis. We obtained similar results in vivo after systemic administration of HDL NPs in mouse lymphoma xenografts and in primary samples obtained from patients with lymphoma. In summary, targeting SCARB1 with HDL NPs in cholesterol uptake-addicted lymphoma cells abolishes GPX4, resulting in cancer cell death by a mechanism consistent with ferroptosis.
|Alternate Journal||J Biol Chem|
|PubMed Central ID||PMC7949030|
|Grant List||R01 CA167041 / CA / NCI NIH HHS / United States |
T32 AR060710 / AR / NIAMS NIH HHS / United States
T32 CA186897 / CA / NCI NIH HHS / United States
T32 HL094293 / HL / NHLBI NIH HHS / United States
Amy Chadburn, M.D.