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- W4221004617 abstract "Alzheimer's disease (AD), an age-related neurodegenerative disease, is a striking global health problem. Ferroptosis is a newly discovered form of cell death characterized by iron-dependent lipid peroxidation products and the accumulation of lethal reactive oxygen species. Strict regulation of iron metabolism is essential to ensure neuronal homeostasis. Excess and deficiency of iron are both associated with neurodegeneration. Studies have shown that oxidative stress caused by cerebral iron metabolism disorders in the body is involved in the process of AD, ferroptosis may play an important role in the pathogenesis of AD, and regulating ferroptosis is expected to be a new direction for the treatment of AD. Various organelles are closely related to ferroptosis: mitochondria, endoplasmic reticulum, Golgi apparatus, and lysosome are involved in the regulation of ferroptosis from the aspects of iron metabolism and redox imbalance. In this review, the relationship between AD and the dysfunction of organelles (including mitochondria, endoplasmic reticulum, lysosome, and Golgi apparatus) and the role of organelles in ferroptosis of AD were reviewed to provide insights for understanding the relationship between organelles and ferroptosis in AD and the treatment of AD." @default.
- W4221004617 created "2022-04-03" @default.
- W4221004617 creator A5006718110 @default.
- W4221004617 creator A5015237817 @default.
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- W4221004617 creator A5030052886 @default.
- W4221004617 creator A5058800301 @default.
- W4221004617 creator A5075782824 @default.
- W4221004617 date "2022-03-16" @default.
- W4221004617 modified "2023-10-06" @default.
- W4221004617 title "The key roles of organelles and ferroptosis in Alzheimerʼs disease" @default.
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