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A graphical journey through iron metabolism, microRNAs, and hypoxia in ferroptosis

Ferroptosis is an iron-dependent form of cell death, which is triggered by disturbed membrane integrity due to an overproduction of lipid peroxides. Induction of ferroptosis comprises several alterations, i.e. altered iron metabolism, response to oxidative stress, or lipid peroxide production. At th...

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Detalles Bibliográficos
Autores principales: Fuhrmann, Dominik C., Brüne, Bernhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213245/
https://www.ncbi.nlm.nih.gov/pubmed/35717888
http://dx.doi.org/10.1016/j.redox.2022.102365
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author Fuhrmann, Dominik C.
Brüne, Bernhard
author_facet Fuhrmann, Dominik C.
Brüne, Bernhard
author_sort Fuhrmann, Dominik C.
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description Ferroptosis is an iron-dependent form of cell death, which is triggered by disturbed membrane integrity due to an overproduction of lipid peroxides. Induction of ferroptosis comprises several alterations, i.e. altered iron metabolism, response to oxidative stress, or lipid peroxide production. At the physiological level transcription, translation, and microRNAs add to the appearance and/or activity of building blocks that negatively or positively balance ferroptosis. Ferroptosis contributes to tissue damage in the case of, e.g., brain and heart injury but may be desirable to overcome chemotherapy resistance. For a more complete picture, it is crucial to also consider the cellular microenvironment, which during inflammation and in the tumor context is dominated by hypoxia. This graphical review visualizes basic mechanisms of ferroptosis, categorizes general inducers and inhibitors of ferroptosis, and puts a focus on microRNAs, iron homeostasis, and hypoxia as regulatory components.
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spelling pubmed-92132452022-06-23 A graphical journey through iron metabolism, microRNAs, and hypoxia in ferroptosis Fuhrmann, Dominik C. Brüne, Bernhard Redox Biol Review Article Ferroptosis is an iron-dependent form of cell death, which is triggered by disturbed membrane integrity due to an overproduction of lipid peroxides. Induction of ferroptosis comprises several alterations, i.e. altered iron metabolism, response to oxidative stress, or lipid peroxide production. At the physiological level transcription, translation, and microRNAs add to the appearance and/or activity of building blocks that negatively or positively balance ferroptosis. Ferroptosis contributes to tissue damage in the case of, e.g., brain and heart injury but may be desirable to overcome chemotherapy resistance. For a more complete picture, it is crucial to also consider the cellular microenvironment, which during inflammation and in the tumor context is dominated by hypoxia. This graphical review visualizes basic mechanisms of ferroptosis, categorizes general inducers and inhibitors of ferroptosis, and puts a focus on microRNAs, iron homeostasis, and hypoxia as regulatory components. Elsevier 2022-06-09 /pmc/articles/PMC9213245/ /pubmed/35717888 http://dx.doi.org/10.1016/j.redox.2022.102365 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review Article
Fuhrmann, Dominik C.
Brüne, Bernhard
A graphical journey through iron metabolism, microRNAs, and hypoxia in ferroptosis
title A graphical journey through iron metabolism, microRNAs, and hypoxia in ferroptosis
title_full A graphical journey through iron metabolism, microRNAs, and hypoxia in ferroptosis
title_fullStr A graphical journey through iron metabolism, microRNAs, and hypoxia in ferroptosis
title_full_unstemmed A graphical journey through iron metabolism, microRNAs, and hypoxia in ferroptosis
title_short A graphical journey through iron metabolism, microRNAs, and hypoxia in ferroptosis
title_sort graphical journey through iron metabolism, micrornas, and hypoxia in ferroptosis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213245/
https://www.ncbi.nlm.nih.gov/pubmed/35717888
http://dx.doi.org/10.1016/j.redox.2022.102365
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