Evidence map›Paper›PMID 37944523›Full record

ArticleCell chemical biology2024

Ferroptosis inhibition by oleic acid mitigates iron-overload-induced injury.

Josiane Mann, Eduard Reznik, Melania Santer, Mark A Fongheiser, Nailah Smith, Tal Hirschhorn, Fereshteh Zandkarimi, Rajesh Kumar Soni, Alcir Luiz Dafré, Antonio Miranda-Vizuete and 2 more

Open access · greenAbstract read
In one paragraph

Article in Cell chemical biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
12.7field-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

51 citing papers in PubMed, 79 citations in OpenAlex.

  1. Article
  2. Article
  3. Ferroptosis as a target mechanism in heart and kidney disease.The Journal of clinical investigation · 2026
    Review
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  14. MAFLD: a ferroptotic disease.Trends in molecular medicine · 2026
    Review
  15. A bezafibrate bearing Pt(IV) prodrug triggers ferroptosis via modulating lipid metabolism in lung cancer cells.Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry · 2026
    Article
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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 4 institutions in 3 countries.

Josiane MannDepartment of Biochemistry, Federal University of Santa Catarina, Florianópolis, Santa Catarina 88040-900, Brazil.
Eduard ReznikDepartment of Biological Sciences, Columbia University, New York, NY 10027, USA.
Melania SanterDepartment of Biochemistry, Federal University of Santa Catarina, Florianópolis, Santa Catarina 88040-900, Brazil.
Mark A FongheiserDepartment of Biological Sciences, Columbia University, New York, NY 10027, USA.
Nailah SmithDepartment of Biological Sciences, Columbia University, New York, NY 10027, USA.
Tal HirschhornDepartment of Biological Sciences, Columbia University, New York, NY 10027, USA.
Fereshteh ZandkarimiDepartment of Chemistry, Columbia University, New York, NY 10027, USA.
Rajesh Kumar SoniHerbert Irving Comprehensive Cancer Center, Columbia University, New York, NY 10032, USA.
Alcir Luiz DafréDepartment of Biochemistry, Federal University of Santa Catarina, Florianópolis, Santa Catarina 88040-900, Brazil.
Antonio Miranda-VizueteInstituto de Biomedicina de Sevilla, IBiS/Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, 41013, Seville, Spain.
Marcelo FarinaDepartment of Biochemistry, Federal University of Santa Catarina, Florianópolis, Santa Catarina 88040-900, Brazil; Department of Biological Sciences, Columbia University, New York, NY 10027, USA. Electronic address: marcelo.farina@ufsc.br.
Brent R StockwellDepartment of Biological Sciences, Columbia University, New York, NY 10027, USA; Herbert Irving Comprehensive Cancer Center, Columbia University, New York, NY 10032, USA; Department of Chemistry, Columbia University, New York, NY 10027, USA; Irving Institute for Cancer Dynamics, Columbia University, New York, NY 10027, USA; Department of Pathology and Cell Biology, Vagelos College of Physicians and Surgeons, Columbia University Irving Medical Center, New York. NY 10032, USA. Electronic address: bstockwell@columbia.edu.
Columbia University · USUniversidade Federal de Santa Catarina · BRColumbia University Irving Medical Center · USInstituto de Biomedicina de Sevilla · ES

Funding

Tumor Biology and Microenvironment ProgramP30CA013696 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Anil K Rustgi · 1985 to 2026
$115.3M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
Defining the functions and translational potential of ferroptosisR35CA209896 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI STOCKWELL, BRENT R. · 2016 to 2022
$6.5M
NCI NIH HHS P30 CA013696NCI NIH HHS R35 CA209896NIH HHS P40 OD010440
6 · The paper itself

Abstract

Iron overload, characterized by accumulation of iron in tissues, induces a multiorgan toxicity whose mechanisms are not fully understood. Using cultured cell lines, Caenorhabditis elegans, and mice, we found that ferroptosis occurs in the context of iron-overload-mediated damage. Exogenous oleic acid protected against iron-overload-toxicity in cell culture and Caenorhabditis elegans by suppressing ferroptosis. In mice, oleic acid protected against FAC-induced liver lipid peroxidation and damage. Oleic acid changed the cellular lipid composition, characterized by decreased levels of polyunsaturated fatty acyl phospholipids and decreased levels of ether-linked phospholipids. The protective effect of oleic acid in cells was attenuated by GW6471 (PPAR-α antagonist), as well as in Caenorhabditis elegans lacking the nuclear hormone receptor NHR-49 (a PPAR-α functional homologue). These results highlight ferroptosis as a driver of iron-overload-mediated damage, which is inhibited by oleic acid. This monounsaturated fatty acid represents a potential therapeutic approach to mitigating organ damage in iron overload individuals.

Indexed as

FerroptosisIron OverloadAnimalsCaenorhabditis elegansIronMiceOleic AcidPeroxisome Proliferator-Activated ReceptorsPhospholipid EthersIronOleic AcidPeroxisome Proliferator-Activated ReceptorsPhospholipid EtherscancerC. eleganscell deathdegenerationferroptosisironlipidMUFAolei acidPPAR

Identifiers

PMID37944523
PMCPMC10922137
OpenAlexW4388489210

What OpenQuestion holds

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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.