Insight Into the Role of Ferroptosis in Non-neoplastic Neurological Diseases
- PMID: 32848622
- PMCID: PMC7424047
- DOI: 10.3389/fncel.2020.00231
Insight Into the Role of Ferroptosis in Non-neoplastic Neurological Diseases
Abstract
Ferroptosis is an iron-dependent form of cell death characterized by the accumulation of intracellular lipid reactive oxygen species (ROS). Ferroptosis is significantly different from other types of cell death including apoptosis, autophagy, and necrosis, both in morphology and biochemical characteristics. The mechanisms that are associated with ferroptosis include iron metabolism, lipid oxidation, and other pathophysiological changes. Ferroptosis inducers or inhibitors can influence its occurrence through different pathways. Ferroptosis was initially discovered in tumors, though recent studies have confirmed that it is also closely related to a variety of neurological diseases including neurodegenerative disease [Alzheimer's disease (AD), Parkinson's disease (PD), etc.] and stroke. This article reviews the definition and characteristics of ferroptosis, the potential mechanisms associated with its development, inducers/inhibitors, and its role in non-neoplastic neurological diseases. We hope to provide a theoretical basis and novel treatment strategies for the treatment of central nervous system diseases by targeting ferroptosis.
Keywords: Alzheimer’s disease; Parkinson’s disease; ferroptosis; iron; neurodegenerative disease; stroke.
Copyright © 2020 Lei, Chen, Song, Sheng, Song and Zhu.
Figures
Similar articles
-
Ferroptosis, a Recent Defined Form of Critical Cell Death in Neurological Disorders.J Mol Neurosci. 2018 Oct;66(2):197-206. doi: 10.1007/s12031-018-1155-6. Epub 2018 Aug 25. J Mol Neurosci. 2018. PMID: 30145632 Review.
-
The Role of Iron Metabolism, Lipid Metabolism, and Redox Homeostasis in Alzheimer's Disease: from the Perspective of Ferroptosis.Mol Neurobiol. 2023 May;60(5):2832-2850. doi: 10.1007/s12035-023-03245-7. Epub 2023 Feb 3. Mol Neurobiol. 2023. PMID: 36735178 Review.
-
Chemically Induced Models of Parkinson's Disease: History and Perspectives for the Involvement of Ferroptosis.Front Cell Neurosci. 2020 Dec 23;14:581191. doi: 10.3389/fncel.2020.581191. eCollection 2020. Front Cell Neurosci. 2020. PMID: 33424553 Free PMC article.
-
Ferroptosis as a Therapeutic Target in Neurodegenerative Diseases: Exploring the Mechanisms and Potential of Treating Alzheimer's Disease and Parkinson's Disease.Protein Pept Lett. 2024;31(10):759-772. doi: 10.2174/0109298665333926240927074528. Protein Pept Lett. 2024. PMID: 39513303 Review.
-
Insight into the potential role of ferroptosis in neurodegenerative diseases.Front Cell Neurosci. 2022 Oct 27;16:1005182. doi: 10.3389/fncel.2022.1005182. eCollection 2022. Front Cell Neurosci. 2022. PMID: 36385946 Free PMC article. Review.
Cited by
-
The Role of AMP-activated Protein Kinase in Oxytosis/Ferroptosis: Protector or Potentiator?Antioxid Redox Signal. 2024 Dec;41(16-18):e1173-e1186. doi: 10.1089/ars.2022.0013. Epub 2022 Apr 8. Antioxid Redox Signal. 2024. PMID: 35243895 Review.
-
Ferroptosis in kidney disease: a bibliometric analysis from 2012 to 2024.Front Pharmacol. 2025 Jan 13;15:1507574. doi: 10.3389/fphar.2024.1507574. eCollection 2024. Front Pharmacol. 2025. PMID: 39872050 Free PMC article. Review.
-
Targeting epigenetic and posttranslational modifications regulating ferroptosis for the treatment of diseases.Signal Transduct Target Ther. 2023 Dec 10;8(1):449. doi: 10.1038/s41392-023-01720-0. Signal Transduct Target Ther. 2023. PMID: 38072908 Free PMC article. Review.
-
Solasodine suppresses nasopharyngeal carcinoma progression by inducing ferroptosis.Sci Rep. 2025 May 18;15(1):17247. doi: 10.1038/s41598-025-93834-4. Sci Rep. 2025. PMID: 40383858 Free PMC article.
-
The research landscape of ferroptosis in neurodegenerative disease: a bibliometric analysis.Front Aging Neurosci. 2024 Jun 17;16:1417989. doi: 10.3389/fnagi.2024.1417989. eCollection 2024. Front Aging Neurosci. 2024. PMID: 38962561 Free PMC article. Review.
References
Publication types
LinkOut - more resources
Full Text Sources