Ferroptosis – Comprehensive review of important cell death mechanism
The authors of the overview article from University Hospital Düsseldorf (from left): Professor Dr Tom Lüdde and Dr Carolin Lohr (Department of Gastroenterology, Hepatology and Infectiology); Leonie Thewes and PD Dr Carsten Berndt (Department of Neurology).
Photo: HHU/Anne Schneider
Overview article in Redox Biology.
An international team comprising 90 authors presents the status of research on “ferroptosis”, a cell death mechanism caused by excess iron and oxygen radicals. Ferroptosis plays an important role in many types of cancer, neurological diseases, stroke, heart attack and other medically relevant situations. Four researchers from Heinrich Heine University Düsseldorf (HHU)/University Hospital Düsseldorf (UKD) have made key contributions to the comprehensive review of this cell death mechanism recently published in the scientific journal Redox Biology.
Ferroptosis is a cell death mechanism that has only become known comparatively recently, being named in 2012. This so-called non-apoptotic cell death occurs when too many oxygen radicals and free iron are present in a cell. Certain molecules in the cell membrane, namely phospholipids, are then oxidised and thereby damaged. Without a corresponding counter-reaction, the cell membrane is eventually destroyed, leading to the death of the cell as a whole.
An entire issue of the scientific journal Redox Biology has now been dedicated to providing a comprehensive summary of existing knowledge of all aspects of ferroptosis. The 90-person, international and interdisciplinary team of authors includes two working groups involving four researchers from HHU, who have made key contributions: Professor Dr Tom Lüdde, Director of the Department of Gastroenterology, Hepatology and Infectiology; PD Dr Carsten Berndt, head of the Thiology research group at the Department of Neurology; Dr Carolin Lohr, Department of Gastroenterology, Hepatology and Infectiology; Leonie Thewes, Department of Neurology. The departments are part of University Hospital Düsseldorf.
Lead author PD Dr Carsten Berndt: “The article highlights the enzymes involved, metabolic requirements, regulatory processes, conditions connected with ferroptosis and experimental methods for investigating this cell death mechanism.”
Ferroptosis occurs under abnormal conditions and has already been described in connection with many pathological conditions. The cell death mechanism plays a key role in all conditions based on a temporarily disrupted oxygen supply caused by reduced blood circulation. These include stroke and heart attack, but the mechanism can also follow many surgical procedures. Ferroptosis is also linked with cancer, neurodegenerative diseases, neuroinflammatory conditions such as multiple sclerosis, kidney disorders and many other conditions.
While Dr Berndt is identifying physiological regulation mechanisms of ferroptosis, Professor Lüdde is examining whether the targeted activation of cell death programmes such as ferroptosis in cancer cells could offer new treatment options, e.g. for cancer of the liver, which can be more precisely targeted and have fewer side effects than conventional chemotherapy options.
The two authors agree: “Several ferroptosis inhibitors aimed at stopping the mechanism are already in clinical trials, as are various ways of triggering ferroptosis in a targeted manner. However, there is still a long way to go before these approaches enter everyday clinical practice.”
Various cell death mechanisms
A differentiation is made between programmed cell death (“apoptosis”) where the organism induces the death of a damaged cell in a targeted and controlled way, unregulated cell death (“necrosis”) and various intermediate levels, of which ferroptosis is one of the most prominent mechanisms. Although there are certain regulatory mechanisms here, the cell ultimately ruptures and releases potentially harmful substances into the surrounding environment in an uncontrolled manner.
Original publication:
Berndt, Alborzinia, Amen, Ayton, Barayeu, Bartelt, Bayir, Bebber, Birsoy, Böttcher, S. Brabletz, T. Brabletz, Brown, Brüne, Bulli, Bruneau, Chen, DeNicola, Dick, Distéfano, Dixon, Engler, Esser-von Bieren, Fedorova, Friedmann Angeli, Friese, Fuhrmann, García-Sáez, Garbowicz, Götz, Gu, Hammerich, Hassannia, Jiang, Jeridi, Kang, Kagan, Konrad, Kotschi, Lei, Le Tertre, Lev, Liang, Linkermann, Lohr, Lorenz, Lüdde, Methner, Michalke, Milton, Min, Mishima, Müller, Motohashi, Muckenthaler, Murakami, Olzmann, Pagnussat, Pan, Papagiannakopoulos, Pedrera Puentes, Pratt, Proneth, Ramsauer, Rodriguez, Saito, Schmidt, Schmitt, Schulze, Schwab, Schwantes, Soula, Spitzlberger, Stockwell, Thewes, Thorn-Seshold, Toyokuni, Tonnus, Trumpp, Vandenabeele, Vanden Berghe, Venkataramani, Vogel, von Karstedt, Wang, Westermann, Wientjens, Wilhelm, Wölk, Wu, Yang, Yu, Zou, Conrad. Ferroptosis in Health and Disease. Redox Biology 75 (2024) 103211
Wissenschaftliche Ansprechpartner:
PD Dr. rer. nat. Carsten Berndt
Carsten.Berndt@med.uni-duesseldorf.de
Originalpublikation:
DOI: 10.1016/j.redox.2024.103211
[Link: https://doi.org/10.1016/j.redox.2024.103211
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