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Mass spectrometry-based approaches to explore metabolism regulating ferroptosis

Ferroptosis is a type of programmed cell death distinct from apoptosis or necroptosis. Ferroptosis is well characterized by an iron-dependent accumulation of lipid peroxides and disruption of cellular membrane integrity. Many metabolic alterations can prevent or accelerate ferroptosis induction. Rec...

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Detalles Bibliográficos
Autores principales: Nguyen, Chi Thi Ngoc, Kim, Seon Min, Kang, Yun Pyo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Biochemistry and Molecular Biology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9537025/
https://www.ncbi.nlm.nih.gov/pubmed/35996835
http://dx.doi.org/10.5483/BMBRep.2022.55.9.109
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author Nguyen, Chi Thi Ngoc
Kim, Seon Min
Kang, Yun Pyo
author_facet Nguyen, Chi Thi Ngoc
Kim, Seon Min
Kang, Yun Pyo
author_sort Nguyen, Chi Thi Ngoc
collection PubMed
description Ferroptosis is a type of programmed cell death distinct from apoptosis or necroptosis. Ferroptosis is well characterized by an iron-dependent accumulation of lipid peroxides and disruption of cellular membrane integrity. Many metabolic alterations can prevent or accelerate ferroptosis induction. Recent advances in analytical techniques of mass spectrometry have allowed high-throughput analysis of metabolites known to be critical for understanding ferroptosis regulatory metabolism. In this review, we introduce mass spectrometry-based analytical methods contributing to recent discovery of various metabolic pathways regulating ferroptosis, focusing on cysteine metabolism, antioxidant metabolism, and poly-unsaturated fatty acid metabolism.
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spelling pubmed-95370252022-10-13 Mass spectrometry-based approaches to explore metabolism regulating ferroptosis Nguyen, Chi Thi Ngoc Kim, Seon Min Kang, Yun Pyo BMB Rep Invited Mini Review Ferroptosis is a type of programmed cell death distinct from apoptosis or necroptosis. Ferroptosis is well characterized by an iron-dependent accumulation of lipid peroxides and disruption of cellular membrane integrity. Many metabolic alterations can prevent or accelerate ferroptosis induction. Recent advances in analytical techniques of mass spectrometry have allowed high-throughput analysis of metabolites known to be critical for understanding ferroptosis regulatory metabolism. In this review, we introduce mass spectrometry-based analytical methods contributing to recent discovery of various metabolic pathways regulating ferroptosis, focusing on cysteine metabolism, antioxidant metabolism, and poly-unsaturated fatty acid metabolism. Korean Society for Biochemistry and Molecular Biology 2022-09-30 2022-09-30 /pmc/articles/PMC9537025/ /pubmed/35996835 http://dx.doi.org/10.5483/BMBRep.2022.55.9.109 Text en Copyright © 2022 by the The Korean Society for Biochemistry and Molecular Biology https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Invited Mini Review
Nguyen, Chi Thi Ngoc
Kim, Seon Min
Kang, Yun Pyo
Mass spectrometry-based approaches to explore metabolism regulating ferroptosis
title Mass spectrometry-based approaches to explore metabolism regulating ferroptosis
title_full Mass spectrometry-based approaches to explore metabolism regulating ferroptosis
title_fullStr Mass spectrometry-based approaches to explore metabolism regulating ferroptosis
title_full_unstemmed Mass spectrometry-based approaches to explore metabolism regulating ferroptosis
title_short Mass spectrometry-based approaches to explore metabolism regulating ferroptosis
title_sort mass spectrometry-based approaches to explore metabolism regulating ferroptosis
topic Invited Mini Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9537025/
https://www.ncbi.nlm.nih.gov/pubmed/35996835
http://dx.doi.org/10.5483/BMBRep.2022.55.9.109
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