Evidence map›Paper›PMID 42457658›Full record

ArticleCell death & disease2026

Remodeling of ferroptotic necroinflammation by dexamethasone in acute tubular necrosis.

Natalie Bethe, Mirela Tmava, Alix Bruneau, Karolin Flade, Benjamin Böhme, Erik Klapproth, Selina Michel, Marlena Nastassja Schlecht, Siyu Xu, Ali El-Armouche and 3 more

Abstract read
In one paragraph

Article in Cell death & disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Natalie Bethe *Medical Clinic and Policlinic 3, University Hospital CGC at the Technische Universität Dresden, Dresden, Germany.
Mirela Tmava *Medical Clinic and Policlinic 3, University Hospital CGC at the Technische Universität Dresden, Dresden, Germany.
Alix BruneauDepartment of Hepatology and Gastroenterology, Campus Charité Mitte and Campus Virchow-Klinikum, Charité-Universitätsmedizin Berlin, Berlin, Germany.ORCID http://orcid.org/0000-0002-5740-2372
Karolin FladeMedical Clinic and Policlinic 3, University Hospital CGC at the Technische Universität Dresden, Dresden, Germany.
Benjamin BöhmeMedical Clinic and Policlinic 3, University Hospital CGC at the Technische Universität Dresden, Dresden, Germany.
Erik KlapprothInstitute of Pharmacology and Toxicology, Technische Universität Dresden, Dresden, Germany.
Selina MichelMedical Clinic and Policlinic 3, University Hospital CGC at the Technische Universität Dresden, Dresden, Germany.
Marlena Nastassja SchlechtMedical Clinic and Policlinic 3, University Hospital CGC at the Technische Universität Dresden, Dresden, Germany.ORCID http://orcid.org/0000-0001-8893-5326
Siyu XuMedical Clinic and Policlinic 3, University Hospital CGC at the Technische Universität Dresden, Dresden, Germany.
Ali El-ArmoucheInstitute of Pharmacology and Toxicology, Technische Universität Dresden, Dresden, Germany.
Frank TackeDepartment of Hepatology and Gastroenterology, Campus Charité Mitte and Campus Virchow-Klinikum, Charité-Universitätsmedizin Berlin, Berlin, Germany.ORCID http://orcid.org/0000-0001-6206-0226
Stefan R BornsteinMedical Clinic and Policlinic 3, University Hospital CGC at the Technische Universität Dresden, Dresden, Germany.
Wulf TonnusMedical Clinic and Policlinic 3, University Hospital CGC at the Technische Universität Dresden, Dresden, Germany. wulf.tonnus@ukdd.de.ORCID http://orcid.org/0000-0002-9728-1413

Funding

Else Kröner-Fresenius-Stiftung (Else Kroner-Fresenius Foundation) 2025_EKES.07
6 · The paper itself

Abstract

Ferroptosis, a modality of regulated necrosis caused by iron-dependent lipid peroxidation, has emerged as a key contributor to the pathogenesis of acute tubular necrosis (ATN) - especially in the context of solid organ transplantation. While recent studies have identified hormones as extracellular signals that modulate cellular susceptibility to ferroptosis, their pathophysiological relevance in vivo remains incompletely defined. Here, we investigated the role of dexamethasone, a potent synthetic glucocorticoid previously reported to sensitize cells to ferroptosis, in the context of renal tubular injury. Unexpectedly, we observed a biphasic effect: early sensitization to ferroptosis induced by glutathione depletion was subsequently counteracted by a marked increase in ferroptosis resistance. Mechanistically, we found that dexamethasone reduced availability of ferrous iron via effects of the glucocorticoid receptor 1 (GR1), which also resulted in attenuated renal tubular injury. However, this cytoprotective effect did not translate into improved renal function, as dexamethasone exerted additional ferroptosis-independent effects on innate immune cell recruitment to injured kidneys. Collectively, our findings highlight the highly dynamic nature of the ferroptotic process in which modulatory signals can exert temporally opposing effects. Moreover, they underscore the complex interplay between regulated cell death and innate immune responses in shaping necroinflammation in disease trajectories.

Indexed as

DexamethasoneFerroptosisInflammationKidney Tubular Necrosis, AcuteAnimalsHumansKidney TubulesMaleMiceMice, Inbred C57BLNecrosisReceptors, GlucocorticoidDexamethasoneReceptors, Glucocorticoid

Identifiers

PMID42457658
PMCPMC13373221

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.