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The glutathione redox system is essential to prevent ferroptosis caused by impaired lipid metabolism in clear cell renal cell carcinoma.
Oncogene. 2018 10; 37(40):5435-5450.O

Abstract

Metabolic reprogramming is a prominent feature of clear cell renal cell carcinoma (ccRCC). Here we investigated metabolic dependencies in a panel of ccRCC cell lines using nutrient depletion, functional RNAi screening and inhibitor treatment. We found that ccRCC cells are highly sensitive to the depletion of glutamine or cystine, two amino acids required for glutathione (GSH) synthesis. Moreover, silencing of enzymes of the GSH biosynthesis pathway or glutathione peroxidases, which depend on GSH for the removal of cellular hydroperoxides, selectively reduced viability of ccRCC cells but did not affect the growth of non-malignant renal epithelial cells. Inhibition of GSH synthesis triggered ferroptosis, an iron-dependent form of cell death associated with enhanced lipid peroxidation. VHL is a major tumour suppressor in ccRCC and loss of VHL leads to stabilisation of hypoxia inducible factors HIF-1α and HIF-2α. Restoration of functional VHL via exogenous expression of pVHL reverted ccRCC cells to an oxidative metabolism and rendered them insensitive to the induction of ferroptosis. VHL reconstituted cells also exhibited reduced lipid storage and higher expression of genes associated with oxidiative phosphorylation and fatty acid metabolism. Importantly, inhibition of β-oxidation or mitochondrial ATP-synthesis restored ferroptosis sensitivity in VHL reconstituted cells. We also found that inhibition of GSH synthesis blocked tumour growth in a MYC-dependent mouse model of renal cancer. Together, our data suggest that reduced fatty acid metabolism due to inhibition of β-oxidation renders renal cancer cells highly dependent on the GSH/GPX pathway to prevent lipid peroxidation and ferroptotic cell death.

Authors+Show Affiliations

Gene Expression Analysis Laboratory, Cancer Research UK London Research Institute, 44 Lincoln's Inn Fields, London, WC2A 3LY, UK. Oncogene Biology Laboratory, The Francis Crick Institute, 1 Midland Road London, London, NW1 1AT, UK.Theodor-Boveri-Institute, Biocenter, Am Hubland, 97074, Würzburg, Germany.Division of Medical Oncology, Stanford University School of Medicine, Stanford, CA, 94305, USA.Institute of Pathology, University Hospital Würzburg, 97080, Würzburg, Germany.Theodor-Boveri-Institute, Biocenter, Am Hubland, 97074, Würzburg, Germany.High Throughput Screening, The Francis Crick Institute, 1 Midland Road London, London, NW1 1AT, UK.High Throughput Screening, The Francis Crick Institute, 1 Midland Road London, London, NW1 1AT, UK.High Throughput Screening, The Francis Crick Institute, 1 Midland Road London, London, NW1 1AT, UK.Oncogene Biology Laboratory, The Francis Crick Institute, 1 Midland Road London, London, NW1 1AT, UK. Division of Cancer Biology, The Institute of Cancer Research, 237 Fulham Road, London, SW7 3RP, UK.Division of Medical Oncology, Stanford University School of Medicine, Stanford, CA, 94305, USA.Gene Expression Analysis Laboratory, Cancer Research UK London Research Institute, 44 Lincoln's Inn Fields, London, WC2A 3LY, UK. Division of Cancer Biology, The Institute of Cancer Research, 237 Fulham Road, London, SW7 3RP, UK.Gene Expression Analysis Laboratory, Cancer Research UK London Research Institute, 44 Lincoln's Inn Fields, London, WC2A 3LY, UK. almut.schulze@uni-wuerzburg.de. Theodor-Boveri-Institute, Biocenter, Am Hubland, 97074, Würzburg, Germany. almut.schulze@uni-wuerzburg.de. Comprehensive Cancer Center Mainfranken, Josef-Schneider-Str.6, 97080, Würzburg, Germany. almut.schulze@uni-wuerzburg.de.

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

29872221

Citation

Miess, Heike, et al. "The Glutathione Redox System Is Essential to Prevent Ferroptosis Caused By Impaired Lipid Metabolism in Clear Cell Renal Cell Carcinoma." Oncogene, vol. 37, no. 40, 2018, pp. 5435-5450.
Miess H, Dankworth B, Gouw AM, et al. The glutathione redox system is essential to prevent ferroptosis caused by impaired lipid metabolism in clear cell renal cell carcinoma. Oncogene. 2018;37(40):5435-5450.
Miess, H., Dankworth, B., Gouw, A. M., Rosenfeldt, M., Schmitz, W., Jiang, M., Saunders, B., Howell, M., Downward, J., Felsher, D. W., Peck, B., & Schulze, A. (2018). The glutathione redox system is essential to prevent ferroptosis caused by impaired lipid metabolism in clear cell renal cell carcinoma. Oncogene, 37(40), 5435-5450. https://doi.org/10.1038/s41388-018-0315-z
Miess H, et al. The Glutathione Redox System Is Essential to Prevent Ferroptosis Caused By Impaired Lipid Metabolism in Clear Cell Renal Cell Carcinoma. Oncogene. 2018;37(40):5435-5450. PubMed PMID: 29872221.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - The glutathione redox system is essential to prevent ferroptosis caused by impaired lipid metabolism in clear cell renal cell carcinoma. AU - Miess,Heike, AU - Dankworth,Beatrice, AU - Gouw,Arvin M, AU - Rosenfeldt,Mathias, AU - Schmitz,Werner, AU - Jiang,Ming, AU - Saunders,Becky, AU - Howell,Michael, AU - Downward,Julian, AU - Felsher,Dean W, AU - Peck,Barrie, AU - Schulze,Almut, Y1 - 2018/06/05/ PY - 2017/09/12/received PY - 2018/04/08/accepted PY - 2018/03/22/revised PY - 2018/6/7/pubmed PY - 2019/2/23/medline PY - 2018/6/7/entrez SP - 5435 EP - 5450 JF - Oncogene JO - Oncogene VL - 37 IS - 40 N2 - Metabolic reprogramming is a prominent feature of clear cell renal cell carcinoma (ccRCC). Here we investigated metabolic dependencies in a panel of ccRCC cell lines using nutrient depletion, functional RNAi screening and inhibitor treatment. We found that ccRCC cells are highly sensitive to the depletion of glutamine or cystine, two amino acids required for glutathione (GSH) synthesis. Moreover, silencing of enzymes of the GSH biosynthesis pathway or glutathione peroxidases, which depend on GSH for the removal of cellular hydroperoxides, selectively reduced viability of ccRCC cells but did not affect the growth of non-malignant renal epithelial cells. Inhibition of GSH synthesis triggered ferroptosis, an iron-dependent form of cell death associated with enhanced lipid peroxidation. VHL is a major tumour suppressor in ccRCC and loss of VHL leads to stabilisation of hypoxia inducible factors HIF-1α and HIF-2α. Restoration of functional VHL via exogenous expression of pVHL reverted ccRCC cells to an oxidative metabolism and rendered them insensitive to the induction of ferroptosis. VHL reconstituted cells also exhibited reduced lipid storage and higher expression of genes associated with oxidiative phosphorylation and fatty acid metabolism. Importantly, inhibition of β-oxidation or mitochondrial ATP-synthesis restored ferroptosis sensitivity in VHL reconstituted cells. We also found that inhibition of GSH synthesis blocked tumour growth in a MYC-dependent mouse model of renal cancer. Together, our data suggest that reduced fatty acid metabolism due to inhibition of β-oxidation renders renal cancer cells highly dependent on the GSH/GPX pathway to prevent lipid peroxidation and ferroptotic cell death. SN - 1476-5594 UR - https://www.unboundmedicine.com/medline/citation/29872221/The_glutathione_redox_system_is_essential_to_prevent_ferroptosis_caused_by_impaired_lipid_metabolism_in_clear_cell_renal_cell_carcinoma_ L2 - http://dx.doi.org/10.1038/s41388-018-0315-z DB - PRIME DP - Unbound Medicine ER -