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FINO(2) Initiates Ferroptosis Through GPX4 Inactivation and Iron Oxidation
Ferroptosis is a non-apoptotic form of regulated cell death caused by the failure of the glutathione-dependent lipid-peroxide-scavenging network. FINO(2) is an endoperoxide-containing 1,2-dioxolane that can initiate ferroptosis selectively in engineered cancer cells. We investigated the mechanism an...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5899674/ https://www.ncbi.nlm.nih.gov/pubmed/29610484 http://dx.doi.org/10.1038/s41589-018-0031-6 |
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author | Gaschler, Michael M. Andia, Alexander A. Liu, Hengrui Csuka, Joleen M. Hurlocker, Brisa Vaiana, Christopher A. Heindel, Daniel W. Zuckerman, Dylan S. Bos, Pieter H. Reznik, Eduard Ye, Lingplak Tyurina, Yulia Y. Lin, Annie J. Shchepinov, Mikhail S. Chan, Amy Y. Peguero-Pereira, Eveliz Fomich, Maksim A. Daniels, Jacob. D. Bekish, Andrei V. Shmanai, Vadim V. Kagan, Valerian E. Mahal, Lara K. Woerpel, Keith A. Stockwell, Brent R. |
author_facet | Gaschler, Michael M. Andia, Alexander A. Liu, Hengrui Csuka, Joleen M. Hurlocker, Brisa Vaiana, Christopher A. Heindel, Daniel W. Zuckerman, Dylan S. Bos, Pieter H. Reznik, Eduard Ye, Lingplak Tyurina, Yulia Y. Lin, Annie J. Shchepinov, Mikhail S. Chan, Amy Y. Peguero-Pereira, Eveliz Fomich, Maksim A. Daniels, Jacob. D. Bekish, Andrei V. Shmanai, Vadim V. Kagan, Valerian E. Mahal, Lara K. Woerpel, Keith A. Stockwell, Brent R. |
author_sort | Gaschler, Michael M. |
collection | PubMed |
description | Ferroptosis is a non-apoptotic form of regulated cell death caused by the failure of the glutathione-dependent lipid-peroxide-scavenging network. FINO(2) is an endoperoxide-containing 1,2-dioxolane that can initiate ferroptosis selectively in engineered cancer cells. We investigated the mechanism and structural features necessary for ferroptosis initiation by FINO(2). We found that FINO(2) requires both an endoperoxide moiety and a nearby hydroxyl head group to initiate ferroptosis. In contrast to previously described ferroptosis inducers, FINO(2) does not inhibit system x(c)(−) or directly target GPX4, as do erastin and RSL3, respectively, or deplete GPX4 protein, as does FIN56. Instead, FINO(2) causes both indirect loss of GPX4 enzymatic function and directly oxidizes iron, ultimately causing widespread lipid peroxidation. These findings suggest that endoperoxides such as FINO(2) can initiate a multi-pronged mechanism of ferroptosis. |
format | Online Article Text |
id | pubmed-5899674 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
spelling | pubmed-58996742018-10-02 FINO(2) Initiates Ferroptosis Through GPX4 Inactivation and Iron Oxidation Gaschler, Michael M. Andia, Alexander A. Liu, Hengrui Csuka, Joleen M. Hurlocker, Brisa Vaiana, Christopher A. Heindel, Daniel W. Zuckerman, Dylan S. Bos, Pieter H. Reznik, Eduard Ye, Lingplak Tyurina, Yulia Y. Lin, Annie J. Shchepinov, Mikhail S. Chan, Amy Y. Peguero-Pereira, Eveliz Fomich, Maksim A. Daniels, Jacob. D. Bekish, Andrei V. Shmanai, Vadim V. Kagan, Valerian E. Mahal, Lara K. Woerpel, Keith A. Stockwell, Brent R. Nat Chem Biol Article Ferroptosis is a non-apoptotic form of regulated cell death caused by the failure of the glutathione-dependent lipid-peroxide-scavenging network. FINO(2) is an endoperoxide-containing 1,2-dioxolane that can initiate ferroptosis selectively in engineered cancer cells. We investigated the mechanism and structural features necessary for ferroptosis initiation by FINO(2). We found that FINO(2) requires both an endoperoxide moiety and a nearby hydroxyl head group to initiate ferroptosis. In contrast to previously described ferroptosis inducers, FINO(2) does not inhibit system x(c)(−) or directly target GPX4, as do erastin and RSL3, respectively, or deplete GPX4 protein, as does FIN56. Instead, FINO(2) causes both indirect loss of GPX4 enzymatic function and directly oxidizes iron, ultimately causing widespread lipid peroxidation. These findings suggest that endoperoxides such as FINO(2) can initiate a multi-pronged mechanism of ferroptosis. 2018-04-02 2018-05 /pmc/articles/PMC5899674/ /pubmed/29610484 http://dx.doi.org/10.1038/s41589-018-0031-6 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Gaschler, Michael M. Andia, Alexander A. Liu, Hengrui Csuka, Joleen M. Hurlocker, Brisa Vaiana, Christopher A. Heindel, Daniel W. Zuckerman, Dylan S. Bos, Pieter H. Reznik, Eduard Ye, Lingplak Tyurina, Yulia Y. Lin, Annie J. Shchepinov, Mikhail S. Chan, Amy Y. Peguero-Pereira, Eveliz Fomich, Maksim A. Daniels, Jacob. D. Bekish, Andrei V. Shmanai, Vadim V. Kagan, Valerian E. Mahal, Lara K. Woerpel, Keith A. Stockwell, Brent R. FINO(2) Initiates Ferroptosis Through GPX4 Inactivation and Iron Oxidation |
title | FINO(2) Initiates Ferroptosis Through GPX4 Inactivation and Iron Oxidation |
title_full | FINO(2) Initiates Ferroptosis Through GPX4 Inactivation and Iron Oxidation |
title_fullStr | FINO(2) Initiates Ferroptosis Through GPX4 Inactivation and Iron Oxidation |
title_full_unstemmed | FINO(2) Initiates Ferroptosis Through GPX4 Inactivation and Iron Oxidation |
title_short | FINO(2) Initiates Ferroptosis Through GPX4 Inactivation and Iron Oxidation |
title_sort | fino(2) initiates ferroptosis through gpx4 inactivation and iron oxidation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5899674/ https://www.ncbi.nlm.nih.gov/pubmed/29610484 http://dx.doi.org/10.1038/s41589-018-0031-6 |
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