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Lipoxygenase‐mediated generation of lipid peroxides enhances ferroptosis induced by erastin and RSL3
- Source :
- Cancer Science
- Publication Year :
- 2017
- Publisher :
- Wiley, 2017.
-
Abstract
- In cancer cells the small compounds erastin and RSL3 promote a novel type of cell death called ferroptosis, which requires iron‐dependent accumulation of lipid reactive oxygen species. Here we assessed the contribution of lipid peroxidation activity of lipoxygenases (LOX) to ferroptosis in oncogenic Ras‐expressing cancer cells. Several 12/15‐LOX inhibitors prevented cell death induced by erastin and RSL3. Furthermore, siRNA‐mediated silencing of ALOX15 significantly decreased both erastin‐induced and RSL3‐induced ferroptotic cell death, whereas exogenous overexpression of ALOX15 enhanced the effect of these compounds. Immunofluorescence analyses revealed that the ALOX15 protein consistently localizes to cell membrane during the course of ferroptosis. Importantly, treatments of cells with ALOX15‐activating compounds accelerated cell death at low, but not high doses of erastin and RSL3. These observations suggest that tumor ferroptosis is promoted by LOX‐catalyzed lipid hydroperoxide generation in cellular membranes.
- Subjects :
- Cell death
0301 basic medicine
Cancer Research
Programmed cell death
Fibrosarcoma
Biology
Piperazines
Cell membrane
Lipid peroxidation
03 medical and health sciences
chemistry.chemical_compound
Lipoxygenase
iron
0302 clinical medicine
Cell, Molecular, and Stem Cell Biology
Cell Line, Tumor
medicine
Arachidonate 15-Lipoxygenase
Humans
Gene silencing
RNA, Small Interfering
glutathione peroxidase
reactive oxygen species
chemistry.chemical_classification
Reactive oxygen species
Glutathione peroxidase
Original Articles
General Medicine
Cell biology
Gene Expression Regulation, Neoplastic
Pancreatic Neoplasms
030104 developmental biology
medicine.anatomical_structure
Oncology
chemistry
030220 oncology & carcinogenesis
Cancer cell
biology.protein
Original Article
Lipid Peroxidation
Carbolines
Ras
Subjects
Details
- ISSN :
- 13497006 and 13479032
- Volume :
- 108
- Database :
- OpenAIRE
- Journal :
- Cancer Science
- Accession number :
- edsair.doi.dedup.....b7219df9626a3feed9d1ffaf4a2f84a3
- Full Text :
- https://doi.org/10.1111/cas.13380