| Literature DB >> 34006412 |
Amir Ajoolabady1, Hamid Aslkhodapasandhokmabad2, Peter Libby3, Jaakko Tuomilehto4, Gregory Y H Lip5, Josef M Penninger6, Des R Richardson7, Daolin Tang8, Hao Zhou9, Shuyi Wang10, Daniel J Klionsky11, Guido Kroemer12, Jun Ren13.
Abstract
Ferroptosis is a form of regulated cell death modality associated with disturbed iron-homeostasis and unrestricted lipid peroxidation. Ample evidence has depicted an essential role for ferroptosis as either the cause or consequence for human diseases, denoting the likely therapeutic promises for targeting ferroptosis in the preservation of human health. Ferritinophagy, a selective form of autophagy, contributes to the initiation of ferroptosis through degradation of ferritin, which triggers labile iron overload (IO), lipid peroxidation, membrane damage, and cell death. In this review, we will delineate the role of ferritinophagy in ferroptosis, and its underlying regulatory mechanisms, to unveil the therapeutic value of ferritinophagy as a target in the combat of ferroptosis to manage metabolic diseases.Entities:
Keywords: ferritinophagy; ferroptosis; iron overload; lipid peroxidation; metabolic diseases
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Year: 2021 PMID: 34006412 DOI: 10.1016/j.tem.2021.04.010
Source DB: PubMed Journal: Trends Endocrinol Metab ISSN: 1043-2760 Impact factor: 12.015