PuSH - Publikationsserver des Helmholtz Zentrums München

Friedmann Angeli, J.P.F. ; Shah, R.* ; Pratt, D.A.* ; Conrad, M.

Ferroptosis inhibition: Mechanisms and opportunities.

Trends Pharmacol. Sci. 38, 489-498 (2017)
Postprint DOI PMC
Open Access Green
The past decade has yielded tremendous insights into how cells die. This has come with our understanding that several distinct forms of cell death are encompassed under the umbrella term necrosis. Among these distinct forms of regulated necrotic cell death, ferroptosis has attracted considerable attention owing to its putative involvement in diverse pathophysiological processes. A key feature of the ferroptosis process is the requirement of phospholipid peroxidation, a process that has been linked with several human pathologies. Now with the establishment of a connection between lipid peroxidation and a distinctive cell death pathway, the search for new small molecules able to suppress lipid peroxidation has gained momentum and may yield novel cytoprotective strategies. We review here advances in our understanding of the ferroptotic process and summarize the development of lipid peroxidation inhibitors with the ultimate goal of suppressing ferroptosis-relevant cell death and related pathologies.
Altmetric
Weitere Metriken?
[➜Einloggen]
Zusatzinfos bearbeiten [➜Einloggen]
Publikationstyp Artikel: Journalartikel
Dokumenttyp Review
Korrespondenzautor
Schlagwörter Cell Death ; Cysteine Metabolism ; Glutathione Peroxidase ; Lipid Peroxidation ; Regulated Necrosis ; Small Molecules; Glutathione-peroxidase 4; Polyunsaturated Fatty-acids; Chain-breaking Antioxidants; Nonapoptotic Cell-death; Vitamin-e; Parkinsons-disease; Oxidative Stress; Huntingtons-disease; Mouse Model; Alox15 Gene
ISSN (print) / ISBN 0165-6147
e-ISSN 1873-3735
Zeitschrift Trends in Pharmacological Sciences
Quellenangaben Band: 38, Heft: 5, Seiten: 489-498 Artikelnummer: , Supplement: ,
Verlag Cell Press
Verlagsort Amsterdam
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Developmental Genetics (IDG)