Pathological breakdown of membrane lipids through excessive lipid peroxidation (LPO) was first described in the mid-20th century and is now recognized as a form of regulated cell death, dubbed ferroptosis. Accumulating evidence unveils how metabolic regulation restrains peroxidation of phospholipids within cellular membranes, thereby impeding ferroptosis execution. Unleashing these metabolic breaks is currently therapeutically explored to sensitize cancers to ferroptosis inducing anti-cancer therapies. Reversely, these natural ferroptotic defense mechanisms can fail resulting in pathological conditions or diseases such as ischemia-reperfusion injury, multi-organ dysfunction, stroke, infarction, or neurodegenerative diseases. This minireview outlines current ferroptosis-inducing anti-cancer strategies and highlights the detection as well as the therapeutic targeting of ferroptosis in preclinical experimental settings. Herein, we also briefly summarize observations related to LPO, iron and redox deregulation in patients that might hint towards ferroptosis as a contributing factor.
-
Cover Image
Cover Image
Single-molecule imaging techniques have revealed the dynamic nature of ion channels and shown that channel activity is sometimes dependent on their mobility and mechanical forces in the lipid membrane. The cover image shows a recent high-resolution cryo-EM image of the two-pore structure of the core complex of the mitochondrial outer membrane protein translocase (TOM) from the filamentous fungus
Neurospora crassa , together with a single-molecule false-color image illustrating the calcium flux through its two pores associated with conformational changes of this protein complex. The TOM core complex undergoes reversible transitions between active (high intensity pink dots), weakly active (medium intensity pink dots) and inactive (low intensity pink dots) channel states corresponding to the suspension of movement. For more information, see the article by Nussberger and colleagues (pp. 911–922) in this issue. Image provided by Shuo Wang.
Therapeutic exploitation of ferroptosis
Magali Walravens, Ine Koeken, Tom Vanden Berghe; Therapeutic exploitation of ferroptosis. Biochem Soc Trans 24 April 2024; 52 (2): 693–706. doi: https://doi.org/10.1042/BST20230550
Download citation file:
Sign in
Sign in to your personal account
Biochemical Society Member Sign in
Sign InSign in via your Institution
Sign in via your InstitutionGet Access To This Article
Cited By
Get Email Alerts
Open Access for all
We offer compliant routes for all authors from 2025. With library support, there will be no author nor reader charges in 5 journals. Check here |
![]() |