Evidence map›Paper›PMID 38441406›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Programming a Ferroptosis-to-Apoptosis Transition Landscape Revealed Ferroptosis Biomarkers and Repressors for Cancer Therapy.

Yaron Vinik, Avi Maimon, Vinay Dubey, Harsha Raj, Ifat Abramovitch, Sergey Malitsky, Maxim Itkin, Avi Ma'ayan, Frank Westermann, Eyal Gottlieb and 2 more

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
15.9field-weighted citation impact, top 1% of its field
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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
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  5. Article
  6. Article
  7. Review
  8. Dissecting Complex Interactions Between Ferroptosis and the Proteasome.bioRxiv : the preprint server for biology · 2026
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Programmed cell death in triple-negative breast cancer.Cellular & molecular biology letters · 2025
    Review
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  18. Review
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  20. Article
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

12 authors at 5 institutions in 3 countries.

Yaron VinikMolecular Cell Biology Department, Weizmann Institute of Science, Rehovot, 76100, Israel.
Avi MaimonMolecular Cell Biology Department, Weizmann Institute of Science, Rehovot, 76100, Israel.
Vinay DubeyMolecular Cell Biology Department, Weizmann Institute of Science, Rehovot, 76100, Israel.
Harsha RajMolecular Cell Biology Department, Weizmann Institute of Science, Rehovot, 76100, Israel.
Ifat AbramovitchThe Ruth and Bruce Rappaport, Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, 3525433, Israel.
Sergey MalitskyMetabolic Profiling Unit, Weizmann Institute of Science, Rehovot, 76100, Israel.
Maxim ItkinMetabolic Profiling Unit, Weizmann Institute of Science, Rehovot, 76100, Israel.
Avi Ma'ayanDepartment of Pharmacological Sciences, Mount Sinai Center for Bioinformatics, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Frank WestermannNeuroblastoma Genomics, German Cancer Research Center (DKFZ), 69120, Heidelberg, Germany.
Eyal GottliebThe Ruth and Bruce Rappaport, Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, 3525433, Israel.
Eytan RuppinCancer Data Science Laboratory, National Cancer Institute, National Institutes of Health, Bethesda, MD, 20892, USA.
Sima LevMolecular Cell Biology Department, Weizmann Institute of Science, Rehovot, 76100, Israel.ORCID 0000-0002-2108-3330
Weizmann Institute of Science · ILTechnion – Israel Institute of Technology · ILGerman Cancer Research Center · DEIcahn School of Medicine at Mount Sinai · USNational Institutes of Health · US

Funding

Computational studies of cancer immunotherapyZIABC011803 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI RUPPIN, EYTAN · 2018 to 2025
$10.7M
Merck KGaA, Darmstadt, GermanyThe Cooperation Program in Cancer Research of the Deutsches Krebsforschungszentrum (DKFZ) and Israel's Ministry of Innovation, Science and Technology (MOST)The Israel Science Foundation 1564/23Weizmann-Pasteur collaborative grant; Erica Drake Fund
6 · The paper itself

Abstract

Ferroptosis and apoptosis are key cell-death pathways implicated in several human diseases including cancer. Ferroptosis is driven by iron-dependent lipid peroxidation and currently has no characteristic biomarkers or gene signatures. Here a continuous phenotypic gradient between ferroptosis and apoptosis coupled to transcriptomic and metabolomic landscapes is established. The gradual ferroptosis-to-apoptosis transcriptomic landscape is used to generate a unique, unbiased transcriptomic predictor, the Gradient Gene Set (GGS), which classified ferroptosis and apoptosis with high accuracy. Further GGS optimization using multiple ferroptotic and apoptotic datasets revealed highly specific ferroptosis biomarkers, which are robustly validated in vitro and in vivo. A subset of the GGS is associated with poor prognosis in breast cancer patients and PDXs and contains different ferroptosis repressors. Depletion of one representative, PDGFA-assaociated protein 1(PDAP1), is found to suppress basal-like breast tumor growth in a mouse model. Omics and mechanistic studies revealed that ferroptosis is associated with enhanced lysosomal function, glutaminolysis, and the tricarboxylic acid (TCA) cycle, while its transition into apoptosis is attributed to enhanced endoplasmic reticulum(ER)-stress and phosphatidylethanolamine (PE)-to-phosphatidylcholine (PC) metabolic shift. Collectively, this study highlights molecular mechanisms underlying ferroptosis execution, identified a highly predictive ferroptosis gene signature with prognostic value, ferroptosis versus apoptosis biomarkers, and ferroptosis repressors for breast cancer therapy.

Indexed as

ApoptosisBiomarkers, TumorFerroptosisAnimalsBiomarkersBreast NeoplasmsCell Line, TumorDisease Models, AnimalFemaleHumansMiceBiomarkersBiomarkers, Tumorapoptosisbiomarkersbreast cancercancer therapyclassification signatureferroptosisTNBC

Identifiers

PMID38441406
PMCPMC11077643
OpenAlexW4392473194

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.