Evidence map›Paper›PMID 41422256›Full record

ArticleCell death & disease2025

Transsulfuration metabolism is essential for ferroptosis resistance in quiescent endothelial cells.

Roxana Elena Oberkersch, Jacopo Lidonnici, Sebastiano Andreuzza, Eleonora Zambon, Gabriele Imperato, Silvia Pedretti, Nico Mitro, Massimo Mattia Santoro

Abstract read
In one paragraph

Article in Cell death & disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

8 authors.

Roxana Elena OberkerschLaboratory of Angiogenesis and Cancer Metabolism, Department of Biology, University of Padua, Padua, Italy.
Jacopo LidonniciLaboratory of Angiogenesis and Cancer Metabolism, Department of Biology, University of Padua, Padua, Italy.ORCID http://orcid.org/0000-0003-1397-1028
Sebastiano AndreuzzaLaboratory of Angiogenesis and Cancer Metabolism, Department of Biology, University of Padua, Padua, Italy.
Eleonora ZambonLaboratory of Angiogenesis and Cancer Metabolism, Department of Biology, University of Padua, Padua, Italy.
Gabriele ImperatoDiSFeB, Department of Pharmacological and Biomolecular Sciences "Rodolfo Paoletti", University of Milan, Milan, Italy.
Silvia PedrettiDiSFeB, Department of Pharmacological and Biomolecular Sciences "Rodolfo Paoletti", University of Milan, Milan, Italy.ORCID http://orcid.org/0000-0001-6404-6321
Nico MitroDiSFeB, Department of Pharmacological and Biomolecular Sciences "Rodolfo Paoletti", University of Milan, Milan, Italy.ORCID http://orcid.org/0000-0002-5000-3619
Massimo Mattia SantoroLaboratory of Angiogenesis and Cancer Metabolism, Department of Biology, University of Padua, Padua, Italy. massimo.santoro@unipd.it.ORCID http://orcid.org/0000-0003-4605-5085

Funding

Associazione Italiana per la Ricerca sul Cancro (Italian Association for Cancer Research) 27028Fondazione Telethon (Telethon Foundation) GGP20003
6 · The paper itself

Abstract

Angiogenesis, the formation of new blood vessels from pre-existing ones, is a crucial process involved in both physiological and pathological contexts. During angiogenesis, quiescent endothelial cells (QECs) forming the vascular bed begin to proliferate and switch their metabolism to support anabolic and energetic needs in response to growth factors and hypoxic conditions. Recent research has demonstrated that ferroptosis, an iron-dependent form of cell death mediated by lipid peroxidation, can affect angiogenesis. Cysteine, a thiol-containing amino acid, is crucial for the synthesis of sulfur-containing biomolecules that control ferroptosis. Glutathione (GSH), a reducing tripeptide containing a cysteine residue, serves as a cofactor for the enzyme glutathione peroxidase 4 (GPX4) to donate electrons to peroxides of polyunsaturated fatty acyl phospholipids. Cysteine can be acquired from its extracellular oxidized form, cystine, via the glutamate-cystine antiporter (system xCT) or synthesized de novo via the transsulfuration pathway (TSP). However, whether proliferating ECs (PECs) and QECs differentially modulate the cysteine/GSH/GPX4 axis to protect themselves from ferroptosis is still unknown. Our findings revealed that PECs primarily utilize extracellular cystine to synthesize GSH, which is essential for avoiding ferroptosis. In contrast, QECs exhibit a resilient response to cystine starvation by activating the TSP. Interestingly, chronic and severe hypoxia induces ferroptosis resistance in PECs exposed to cystine limitation, mimicking the metabolic profile of QECs. Molecularly, QECs exhibit high NRF2 expression necessary to support TSP under cystine limitation and protect QECs from ferroptosis. In vivo experiments confirm the susceptibility of ECs to cell death by xCT inhibition in a retinal model of sprouting angiogenesis. These findings highlight differential regulation of cysteine metabolism in PECs and QECs and suggest that the cysteine/GSH/GPX4 axis could be a potential therapeutic target for diseases involving angiogenesis.

Indexed as

Endothelial CellsFerroptosisSulfurAmino Acid Transport System y+AnimalsCysteineGlutathioneHumansMiceMice, Inbred C57BLNF-E2-Related Factor 2Phospholipid Hydroperoxide Glutathione PeroxidaseAmino Acid Transport System y+CysteineGlutathioneNF-E2-Related Factor 2Phospholipid Hydroperoxide Glutathione PeroxidaseSulfur

Identifiers

PMID41422256
PMCPMC12847926

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.