Evidence map›Paper›PMID 35271393›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Ferroptosis regulation by the NGLY1/NFE2L1 pathway.

Giovanni C Forcina, Lauren Pope, Magdalena Murray, Wentao Dong, Monther Abu-Remaileh, Carolyn R Bertozzi, Scott J Dixon

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
14.1field-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

59 citing papers in PubMed, 98 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Dissecting Complex Interactions Between Ferroptosis and the Proteasome.bioRxiv : the preprint server for biology · 2026
    Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Recommendations for robust and reproducible research on ferroptosis.Nature reviews. Molecular cell biology · 2025
    Review
  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

7 authors at 1 institution in 1 country.

Giovanni C ForcinaDepartment of Biology, Stanford University, Stanford, CA 94305.
Lauren PopeDepartment of Biology, Stanford University, Stanford, CA 94305.
Magdalena MurrayDepartment of Biology, Stanford University, Stanford, CA 94305.
Wentao DongDepartment of Chemical Engineering, Stanford University, Stanford, CA 94305.ORCID 0000-0001-5490-4265
Monther Abu-RemailehDepartment of Chemical Engineering, Stanford University, Stanford, CA 94305.
Carolyn R BertozziStanford ChEM-H, Stanford University, Stanford, CA 94305.ORCID 0000-0003-4482-2754
Scott J DixonDepartment of Biology, Stanford University, Stanford, CA 94305.ORCID 0000-0001-6230-8199
Stanford University · US

Funding

Targeting the Cancer GlycocalyxR01CA227942 · NCI · STANFORD UNIVERSITY · PI Carolyn Bertozzi · 2019 to 2026
$3.6M
Characterizing the Regulation of FerroptosisR01GM122923 · NIGMS · STANFORD UNIVERSITY · PI Scott Dixon · 2017 to 2026
$3.4M
Glycosylation and Immune Evasion in Urologic TumorsU01CA226051 · NCI · STANFORD UNIVERSITY · PI BERTOZZI, CAROLYN, BROOKS, JAMES D. · 2019 to 2023
$3.0M
NCI NIH HHS R01 CA227942NCI NIH HHS U01 CA226051NIGMS NIH HHS R01 GM122923
6 · The paper itself

Abstract

SignificanceFerroptosis is an oxidative form of cell death whose biochemical regulation remains incompletely understood. Cap'n'collar (CNC) transcription factors including nuclear factor erythroid-2-related factor 1 (NFE2L1/NRF1) and NFE2L2/NRF2 can both regulate oxidative stress pathways but are each regulated in a distinct manner, and whether these two transcription factors can regulate ferroptosis independent of one another is unclear. We find that NFE2L1 can promote ferroptosis resistance, independent of NFE2L2, by maintaining the expression of glutathione peroxidase 4 (GPX4), a key protein that prevents lethal lipid peroxidation. NFE2L2 can also promote ferroptosis resistance but does so through a distinct mechanism that appears independent of GPX4 protein expression. These results suggest that NFE2L1 and NFE2L2 independently regulate ferroptosis.

Indexed as

FerroptosisGene Expression RegulationNF-E2-Related Factor 1Oxidative StressPeptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine AmidasePhospholipid Hydroperoxide Glutathione PeroxidaseGene Knockout TechniquesHumansLipid PeroxidationMetabolic Networks and PathwaysNFE2L1 protein, humanNF-E2-Related Factor 1NGLY1 protein, humanPeptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine AmidasePhospholipid Hydroperoxide Glutathione PeroxidasecancerferroptosisNRF1

Identifiers

PMID35271393
PMCPMC8931371
OpenAlexW4220813238

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.