Ferroptosis in Different Pathological Contexts Seen through the Eyes of Mitochondria
2021
Тип документа:
Чланак у часопису (Објављена верзија)
Метаподаци
Приказ свих података о документуАпстракт:
Ferroptosis is a recently described form of regulated cell death characterized by intracellular iron accumulation and severe lipid peroxidation due to an impaired cysteine-glutathione-glutathione peroxidase 4 antioxidant defence axis. One of the hallmarks of ferroptosis is a specific morphological phenotype characterized by extensive ultrastructural changes of mitochondria. Increasing evidence suggests that mitochondria play a significant role in the induction and execution of ferroptosis. The present review summarizes existing knowledge about the mitochondrial impact on ferroptosis in different pathological states, primarily cancer, cardiovascular diseases, and neurodegenerative diseases. Additionally, we highlight pathologies in which the ferroptosis/mitochondria relation remains to be investigated, where the process of ferroptosis has been confirmed (such as liver- and kidney-related pathologies) and those in which ferroptosis has not been studied yet, such as diabetes. We will bring attention to avenues that could be followed in future research, based on the use of mitochondria-targeted approaches as anti- and proferroptotic strategies and directed to the improvement of existing and the development of novel therapeutic strategies.
Кључне речи:
ferroptosis; mitochondria; lipid peroxide; reactive oxygen speciesИзвор:
Oxidative Medicine and Cellular Longevity, 2021, 2021, 1-16Финансирање / пројекти:
- Министарство науке, технолошког развоја и иновација Републике Србије, институционално финансирање - 200007 (Универзитет у Београду, Институт за биолошка истраживања 'Синиша Станковић') (RS-MESTD-inst-2020-200007)
- Science Fund of the Republic of Serbia (Serbian Science and Diaspora Collaboration Program: Knowledge Exchange Vouchers, #Grant No. 6525651, Ferroptosis in the β-cells death: possible strategy for diabetes treatment, acronym: BetFeSis)
DOI: 10.1155/2021/5537330
ISSN: 1942-0900
PubMed: 34211625
WoS: 000665763100001
Scopus: 2-s2.0-85108534958
URI
https://www.hindawi.com/journals/omcl/2021/5537330/https://radar.ibiss.bg.ac.rs/handle/123456789/4417