Molecular mechanisms of ferroptosis and their involvement in brain diseases

被引:203
作者
Costa, Ines [1 ,2 ]
Barbosa, Daniel Jose [3 ,4 ]
Benfeito, Sofia [5 ]
Silva, Vera [1 ,2 ]
Chavarria, Daniel
Borges, Fernanda
Remiao, Fernando [1 ,2 ]
Silva, Renata [1 ,2 ]
机构
[1] Univ Porto, Inst Hlth & Bioecon, Fac Pharm, Associate Lab i4HB, P-4050313 Porto, Portugal
[2] Univ Porto, Fac Pharm, Dept Biol Sci, UCIBIO Appl Mol Biosci Unit,Lab Toxicol, P-4050313 Porto, Portugal
[3] Univ Inst Hlth Sci, Dept Sci, TOXRUN Toxicol Res Unit, CESPU,CRL, P-4585116 Gandra, Portugal
[4] Univ Porto, Inst Invest & Inovacao Saude i3S, P-4200135 Porto, Portugal
[5] Univ Porto, Fac Sci, Dept Chem & Biochem, CIQUP IMS, R Campo Alegre S-N, P-4169007 Porto, Portugal
关键词
Ferroptosis inducers; Ferroptosis inhibitors Brain diseases; Ferroptosis; Ferroptosis mechanisms; GLUTATHIONE-PEROXIDASE; 4; AMYOTROPHIC-LATERAL-SCLEROSIS; DEPENDENT LIPID-PEROXIDATION; POLYUNSATURATED FATTY-ACIDS; IRON REGULATORY PROTEIN-1; CELL-DEATH; OXIDATIVE STRESS; ALPHA-SYNUCLEIN; HUNTINGTONS-DISEASE; PARKINSONS-DISEASE;
D O I
10.1016/j.pharmthera.2023.108373
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ferroptosis is a type of regulated cell death characterized by intracellular accumulation of iron and reactive oxy-gen species, inhibition of system Xc-, glutathione depletion, nicotinamide adenine dinucleotide phosphate oxida-tion and lipid peroxidation. Since its discovery and characterization in 2012, many efforts have been made to reveal the underlying mechanisms, modulating compounds, and its involvement in disease pathways.Ferroptosis inducers include erastin, sorafenib, sulfasalazine and glutamate, which, by inhibiting system Xc-, pre-vent the import of cysteine into the cells. RSL3, statins, Ml162 and Ml210 induce ferroptosis by inhibiting gluta-thione peroxidase 4 (GPX4), which is responsible for preventing the formation of lipid peroxides, and FIN56 and withaferin trigger GPX4 degradation. On the other side, ferroptosis inhibitors include ferrostatin-1, liproxstatin-1, alpha-tocopherol, zileuton, FSP1, CoQ10 and BH4, which interrupt the lipid peroxidation cascade. Additionally, deferoxamine, deferiprone and N-acetylcysteine, by targeting other cellular pathways, have also been classified as ferroptosis inhibitors.Increased evidence has established the involvement of ferroptosis in distinct brain diseases, including Alzheimer's, Parkinson's and Huntington's diseases, amyotrophic lateral sclerosis, multiple sclerosis, and Friedreich's ataxia. Thus, a deep understanding of how ferroptosis contributes to these diseases, and how it can be modulated, can open a new window of opportunities for novel therapeutic strategies and targets. Other stud-ies have shown a sensitivity of cancer cells with mutated RAS to ferroptosis induction and that chemotherapeutic agents and ferroptosis inducers synergize in tumor treatment. Thus, it is tempting to consider that ferroptosis may arise as a target mechanistic pathway for the treatment of brain tumors.Therefore, this work provides an up-to-date review on the molecular and cellular mechanisms of ferroptosis and their involvement in brain diseases. In addition, information on the main ferroptosis inducers and inhibitors and their molecular targets is also provided.(c) 2023 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http:// creativecommons.org/licenses/by-nc-nd/4.0/).
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页数:32
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