Evidence map›Paper›PMID 40233740›Full record

ArticleCell2025

ALDH7A1 protects against ferroptosis by generating membrane NADH and regulating FSP1.

Jia-Shu Yang, Andrew J Morris, Koki Kamizaki, Jianzhong Chen, Jillian Stark, William M Oldham, Toshitaka Nakamura, Eikan Mishima, Joseph Loscalzo, Yasuhiro Minami and 3 more

Abstract read
In one paragraph

Article in Cell, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
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  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. ERM Inhibition Confers Ferroptosis Resistance through ROS-Induced NRF2 Signaling.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  15. Article
  16. Review
  17. Membrane Stress and Ferroptosis: Lipid Dynamics in Cancer.International journal of molecular sciences · 2026
    Review
  18. Article
  19. Review
  20. 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

13 authors.

Jia-Shu YangDivision of Rheumatology, Inflammation and Immunity, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA. Electronic address: jyang1@bwh.harvard.edu.
Andrew J MorrisDivision of Cardiovascular Medicine, Department of Medicine, University of Kentucky and Lexington Veterans Affairs Medical Center, Lexington, KY 40536, USA; Central Arkansas VA Healthcare System and Arkansas Children's Nutrition Research Center, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Koki KamizakiDepartment of Physiology and Cell Biology, Kobe University School of Medicine, Kobe 650-0017, Japan.
Jianzhong ChenDivision of Cardiovascular Medicine, Department of Medicine, University of Kentucky and Lexington Veterans Affairs Medical Center, Lexington, KY 40536, USA.
Jillian StarkDepartment of Biology, Massachusetts Institute of Technology, and Koch Institute for Integrative Cancer Research, Cambridge, MA 02139, USA.
William M OldhamDivision of Pulmonary and Critical Care Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.
Toshitaka NakamuraInstitute of Metabolism and Cell Death, Molecular Targets and Therapeutics Center, Helmholtz Munich, Neuherberg, Germany.
Eikan MishimaInstitute of Metabolism and Cell Death, Molecular Targets and Therapeutics Center, Helmholtz Munich, Neuherberg, Germany.
Joseph LoscalzoCardiovascular Division, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.
Yasuhiro MinamiDepartment of Physiology and Cell Biology, Kobe University School of Medicine, Kobe 650-0017, Japan.
Marcus ConradInstitute of Metabolism and Cell Death, Molecular Targets and Therapeutics Center, Helmholtz Munich, Neuherberg, Germany.
Whitney S HenryDepartment of Biology, Massachusetts Institute of Technology, and Koch Institute for Integrative Cancer Research, Cambridge, MA 02139, USA.
Victor W HsuDivision of Rheumatology, Inflammation and Immunity, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA. Electronic address: vhsu@bwh.harvard.edu.

Funding

Mechanisms and Physiology of COPI TransportR37GM058615 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI HSU, VICTOR W · 2016 to 2025
$6.0M
L-2-Hydroxyglutarate and Metabolic Remodeling in HypoxiaR01HL155107 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI Joseph Loscalzo · 2021 to 2026
$4.1M
Role of lactate transporters in pulmonary fibrosisR01HL167718 · NHLBI · RHODE ISLAND HOSPITAL · PI William Michael Oldham · 2023 to 2026
$3.4M
Branched-chain Keto-acids and Aerobic Glycolysis in Vascular Smooth Muscle CellsR01HL166137 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI Joseph Loscalzo · 2023 to 2026
$2.8M
Personalized protein-protein interactomes and precision medicine in pulmonary arterial hypertensionR01HL155096 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI MARON, BRADLEY · 2021 to 2024
$1.6M
Regulation of pulmonary vascular cell redox state by L-2-hydroxyglutarateK08HL128802 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI OLDHAM, WILLIAM MICHAEL · 2016 to 2020
$862k
BLRD VA I01 BX004671BLRD VA I01 BX005637BLRD VA IK6 BX006469CSRD VA I01 CX001550NHLBI NIH HHS K08 HL128802NHLBI NIH HHS R01 HL155096NHLBI NIH HHS R01 HL155107NHLBI NIH HHS R01 HL166137NHLBI NIH HHS R01 HL167718NIGMS NIH HHS R37 GM058615
6 · The paper itself

Abstract

Ferroptosis is a form of cell death due to iron-induced lipid peroxidation. Ferroptosis suppressor protein 1 (FSP1) protects against this death by generating antioxidants, which requires nicotinamide adenine dinucleotide, reduced form (NADH) as a cofactor. We initially uncover that NADH exists at significant levels on cellular membranes and then find that this form of NADH is generated by aldehyde dehydrogenase 7A1 (ALDH7A1) to support FSP1 activity. ALDH7A1 activity also acts directly to decrease lipid peroxidation by consuming reactive aldehydes. Furthermore, ALDH7A1 promotes the membrane recruitment of FSP1, which is instigated by ferroptotic stress activating AMP-activated protein kinase (AMPK) to promote the membrane localization of ALDH7A1 that stabilizes FSP1 on membranes. These findings advance a fundamental understanding of NADH by revealing a previously unappreciated pool on cellular membranes, with the elucidation of its function providing a major understanding of how FSP1 acts and how an aldehyde dehydrogenase protects against ferroptosis.

Indexed as

Aldehyde DehydrogenaseCell MembraneFerroptosisNADAMP-Activated Protein KinasesAnimalsHEK293 CellsHumansLipid PeroxidationMiceAldehyde DehydrogenaseAMP-Activated Protein KinasesNADaldehyde dehydrogenase 7A1ferroptosisferroptosis suppressor protein 1nicotinamide adenine dinucleotide reduced form

Identifiers

PMID40233740
PMCPMC12085291

What OpenQuestion holds

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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.