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Lipoxygenase‐mediated generation of lipid peroxides enhances ferroptosis induced by erastin and RSL3
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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666033/ https://www.ncbi.nlm.nih.gov/pubmed/28837253 http://dx.doi.org/10.1111/cas.13380 |
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author | Shintoku, Ryosuke Takigawa, Yuta Yamada, Keiichi Kubota, Chisato Yoshimoto, Yuhei Takeuchi, Toshiyuki Koshiishi, Ichiro Torii, Seiji |
author_facet | Shintoku, Ryosuke Takigawa, Yuta Yamada, Keiichi Kubota, Chisato Yoshimoto, Yuhei Takeuchi, Toshiyuki Koshiishi, Ichiro Torii, Seiji |
author_sort | Shintoku, Ryosuke |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5666033 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56660332017-11-09 Lipoxygenase‐mediated generation of lipid peroxides enhances ferroptosis induced by erastin and RSL3 Shintoku, Ryosuke Takigawa, Yuta Yamada, Keiichi Kubota, Chisato Yoshimoto, Yuhei Takeuchi, Toshiyuki Koshiishi, Ichiro Torii, Seiji Cancer Sci Original Articles 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. John Wiley and Sons Inc. 2017-09-15 2017-11 /pmc/articles/PMC5666033/ /pubmed/28837253 http://dx.doi.org/10.1111/cas.13380 Text en © 2017 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Shintoku, Ryosuke Takigawa, Yuta Yamada, Keiichi Kubota, Chisato Yoshimoto, Yuhei Takeuchi, Toshiyuki Koshiishi, Ichiro Torii, Seiji Lipoxygenase‐mediated generation of lipid peroxides enhances ferroptosis induced by erastin and RSL3 |
title | Lipoxygenase‐mediated generation of lipid peroxides enhances ferroptosis induced by erastin and RSL3 |
title_full | Lipoxygenase‐mediated generation of lipid peroxides enhances ferroptosis induced by erastin and RSL3 |
title_fullStr | Lipoxygenase‐mediated generation of lipid peroxides enhances ferroptosis induced by erastin and RSL3 |
title_full_unstemmed | Lipoxygenase‐mediated generation of lipid peroxides enhances ferroptosis induced by erastin and RSL3 |
title_short | Lipoxygenase‐mediated generation of lipid peroxides enhances ferroptosis induced by erastin and RSL3 |
title_sort | lipoxygenase‐mediated generation of lipid peroxides enhances ferroptosis induced by erastin and rsl3 |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666033/ https://www.ncbi.nlm.nih.gov/pubmed/28837253 http://dx.doi.org/10.1111/cas.13380 |
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