Evidence map›Paper›PMID 35174317›Full record

ArticleCell stress2022

MYCN upregulates the transsulfuration pathway to suppress the ferroptotic vulnerability in

Konstantinos V Floros, Ayesha T Chawla, Mia O Johnson-Berro, Rishabh Khatri, Angeliki M Stamatouli, Sosipatros A Boikos, Mikhail G Dozmorov, L Ashley Cowart, Anthony C Faber

Open access · goldAbstract read
In one paragraph

Article in Cell stress, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 23 citations in OpenAlex.

  1. Targeted extracellular degradation of LRP8 promotes ferroptosis in cancer cells.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  13. Ferroptosis in cancer (Review).Oncology letters · 2024
    Review
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  18. Ferroptosis inhibitors: past, present and future.Frontiers in pharmacology · 2024
    Review
  19. Tryptophan Metabolism Acts as a New Anti-Ferroptotic Pathway to Mediate Tumor Growth.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
  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

9 authors at 2 institutions in 1 country.

Konstantinos V FlorosDepartment of Oral and Craniofacial Molecular Biology, Philips Institute for Oral Health Research, VCU School of Dentistry and Massey Cancer Center, Virginia Commonwealth University, Richmond, VA, USA.
Ayesha T ChawlaDepartment of Oral and Craniofacial Molecular Biology, Philips Institute for Oral Health Research, VCU School of Dentistry and Massey Cancer Center, Virginia Commonwealth University, Richmond, VA, USA.
Mia O Johnson-BerroDepartment of Oral and Craniofacial Molecular Biology, Philips Institute for Oral Health Research, VCU School of Dentistry and Massey Cancer Center, Virginia Commonwealth University, Richmond, VA, USA.
Rishabh KhatriDepartment of Oral and Craniofacial Molecular Biology, Philips Institute for Oral Health Research, VCU School of Dentistry and Massey Cancer Center, Virginia Commonwealth University, Richmond, VA, USA.
Angeliki M StamatouliDivision of Endocrinology, Diabetes, and Metabolism, Department of Internal Medicine, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
Sosipatros A BoikosDivision of Hematology, Oncology and Palliative Care, Virginia Commonwealth University and Massey Cancer Center, Richmond, VA, USA.
Mikhail G DozmorovDepartment of Biostatistics, Virginia Commonwealth University, Richmond, VA, USA.
L Ashley CowartDepartment of Biochemistry and Molecular Biology and Massey Cancer Center, Virginia Commonwealth University, Richmond, VA, USA.
Anthony C FaberDepartment of Oral and Craniofacial Molecular Biology, Philips Institute for Oral Health Research, VCU School of Dentistry and Massey Cancer Center, Virginia Commonwealth University, Richmond, VA, USA.
Virginia Commonwealth University · USHunter Holmes McGuire VA Medical Center · US

Funding

Virus Vector Shared ResourceP30CA016059 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI Kim Felder Rhoads · 1985 to 2026
$51.0M
ABT-199 based therapies to treat neuroblastomaR01CA215610 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI Anthony Charles Faber · 2017 to 2026
$2.9M
Novel sphingolipid metabolites in myocardial ischemiaR01HL151243 · NHLBI · VIRGINIA COMMONWEALTH UNIVERSITY · PI COWART, LAUREN ASHLEY · 2020 to 2024
$1.9M
Sphingolipids in the Pathophysiology of Obesity and DiabetesI01BX000200 · VA · VA VETERANS ADMINISTRATION HOSPITAL · PI COWART, LAUREN ASHLEY · 2009 to 2025
–
BLRD VA I01 BX000200BLRD VA IK6 BX006315NCI NIH HHS P30 CA016059NCI NIH HHS R01 CA215610NHLBI NIH HHS R01 HL151243
6 · The paper itself

Abstract

Ferroptosis is an iron-dependent, oxidative form of cell death that is countered mainly by glutathione peroxidase 4 (GPX4) and the production of glutathione (GSH), which is formed from cysteine. The identification of the cancers that may benefit from pharmacological ferroptotic induction is just emerging. We recently demonstrated that inducing ferroptosis genetically or pharmacologically in

Indexed as

cystathioninecysteineferroptosismethionineMYCN-amplified neuroblastomatranssulfuration pathway

Identifiers

PMID35174317
PMCPMC8802432
OpenAlexW4210310874

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.