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Organelle-Specific Mechanisms in Crosstalk between Apoptosis and Ferroptosis

Apoptosis has been extensively studied, whereas ferroptosis is a newly discovered form of regulated cell death that involves iron-dependent accumulations of lipid hydroperoxides. While these two cell death mechanisms were initially believed to be mutually exclusive, recent studies have revealed cell...

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Detalles Bibliográficos
Autores principales: Wu, Peiyao, Zhang, Xiaoyue, Duan, Dingyu, Zhao, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9836800/
https://www.ncbi.nlm.nih.gov/pubmed/36644574
http://dx.doi.org/10.1155/2023/3400147
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author Wu, Peiyao
Zhang, Xiaoyue
Duan, Dingyu
Zhao, Lei
author_facet Wu, Peiyao
Zhang, Xiaoyue
Duan, Dingyu
Zhao, Lei
author_sort Wu, Peiyao
collection PubMed
description Apoptosis has been extensively studied, whereas ferroptosis is a newly discovered form of regulated cell death that involves iron-dependent accumulations of lipid hydroperoxides. While these two cell death mechanisms were initially believed to be mutually exclusive, recent studies have revealed cellular contexts requiring a balanced interaction between them. Numerous subcellular sites and signaling molecules within these sites are involved in both processes, either as modules or switches that allow cells to choose on how to proceed. The close relationships between apoptosis and ferroptosis, as well as the possibility of switching from one to the other, are described in this review. To understand the crosstalk between apoptosis and ferroptosis, various organelle-specific mechanisms must be analyzed and compared. The ability to switch apoptosis to ferroptosis by targeting cellular organelles has a great potential in cancer therapy.
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spelling pubmed-98368002023-01-13 Organelle-Specific Mechanisms in Crosstalk between Apoptosis and Ferroptosis Wu, Peiyao Zhang, Xiaoyue Duan, Dingyu Zhao, Lei Oxid Med Cell Longev Review Article Apoptosis has been extensively studied, whereas ferroptosis is a newly discovered form of regulated cell death that involves iron-dependent accumulations of lipid hydroperoxides. While these two cell death mechanisms were initially believed to be mutually exclusive, recent studies have revealed cellular contexts requiring a balanced interaction between them. Numerous subcellular sites and signaling molecules within these sites are involved in both processes, either as modules or switches that allow cells to choose on how to proceed. The close relationships between apoptosis and ferroptosis, as well as the possibility of switching from one to the other, are described in this review. To understand the crosstalk between apoptosis and ferroptosis, various organelle-specific mechanisms must be analyzed and compared. The ability to switch apoptosis to ferroptosis by targeting cellular organelles has a great potential in cancer therapy. Hindawi 2023-01-05 /pmc/articles/PMC9836800/ /pubmed/36644574 http://dx.doi.org/10.1155/2023/3400147 Text en Copyright © 2023 Peiyao Wu et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Wu, Peiyao
Zhang, Xiaoyue
Duan, Dingyu
Zhao, Lei
Organelle-Specific Mechanisms in Crosstalk between Apoptosis and Ferroptosis
title Organelle-Specific Mechanisms in Crosstalk between Apoptosis and Ferroptosis
title_full Organelle-Specific Mechanisms in Crosstalk between Apoptosis and Ferroptosis
title_fullStr Organelle-Specific Mechanisms in Crosstalk between Apoptosis and Ferroptosis
title_full_unstemmed Organelle-Specific Mechanisms in Crosstalk between Apoptosis and Ferroptosis
title_short Organelle-Specific Mechanisms in Crosstalk between Apoptosis and Ferroptosis
title_sort organelle-specific mechanisms in crosstalk between apoptosis and ferroptosis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9836800/
https://www.ncbi.nlm.nih.gov/pubmed/36644574
http://dx.doi.org/10.1155/2023/3400147
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