Friedreich's ataxia (FRDA) is a neurodegenerative disease characterized by early mortality due to hypertrophic cardiomyopathy. FRDA is caused by reduced levels of frataxin (FXN), a mitochondrial protein involved in the synthesis of iron-sulphur clusters, leading to iron accumulation at the mitochondrial level, uncontrolled production of reactive oxygen species and lipid peroxidation. These features are also common to ferroptosis, an iron-mediated type of cell death triggered by accumulation of lipoperoxides with distinct morphological and molecular characteristics with respect to other known cell deaths.
Turchi, R., Faraonio, R., Lettieri-Barbato, D., Aquilano, K. (2020). An Overview of the Ferroptosis Hallmarks in Friedreich's Ataxia. BIOMOLECULES, 10(11) [10.3390/biom10111489].
An Overview of the Ferroptosis Hallmarks in Friedreich's Ataxia
Lettieri-Barbato, Daniele;Aquilano, Katia
2020-10-28
Abstract
Friedreich's ataxia (FRDA) is a neurodegenerative disease characterized by early mortality due to hypertrophic cardiomyopathy. FRDA is caused by reduced levels of frataxin (FXN), a mitochondrial protein involved in the synthesis of iron-sulphur clusters, leading to iron accumulation at the mitochondrial level, uncontrolled production of reactive oxygen species and lipid peroxidation. These features are also common to ferroptosis, an iron-mediated type of cell death triggered by accumulation of lipoperoxides with distinct morphological and molecular characteristics with respect to other known cell deaths.File | Dimensione | Formato | |
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