BID links ferroptosis to mitochondrial cell death pathways

Ferroptosis has been defined as an oxidative and iron-dependent pathway of regulated cell death that is distinct from caspase-dependent apoptosis and established pathways of death receptor-mediated regulated necrosis. While emerging evidence linked features of ferroptosis induced e.g. by erastin-med...

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Hauptverfasser: Neitemeier, Sandra (VerfasserIn) , Oppermann, Sina (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: August 2017
In: Redox Biology
Year: 2017, Jahrgang: 12, Pages: 558-570
ISSN:2213-2317
DOI:10.1016/j.redox.2017.03.007
Online-Zugang:Resolving-System, Volltext: http://dx.doi.org/10.1016/j.redox.2017.03.007
Verlag, Volltext: https://www.sciencedirect.com/science/article/pii/S2213231717300654
Volltext
Verfasserangaben:Sandra Neitemeier, Anja Jelinek, Vincenzo Laino, Lena Hoffmann, Ina Eisenbach, Roman Eying, Goutham K. Ganjam, Amalia M. Dolga, Sina Oppermann, Carsten Culmsee
Beschreibung
Zusammenfassung:Ferroptosis has been defined as an oxidative and iron-dependent pathway of regulated cell death that is distinct from caspase-dependent apoptosis and established pathways of death receptor-mediated regulated necrosis. While emerging evidence linked features of ferroptosis induced e.g. by erastin-mediated inhibition of the Xc- system or inhibition of glutathione peroxidase 4 (Gpx4) to an increasing number of oxidative cell death paradigms in cancer cells, neurons or kidney cells, the biochemical pathways of oxidative cell death remained largely unclear. In particular, the role of mitochondrial damage in paradigms of ferroptosis needs further investigation.
Beschreibung:Available online 9 March 2017
Gesehen am 22.10.2018
Beschreibung:Online Resource
ISSN:2213-2317
DOI:10.1016/j.redox.2017.03.007