Evidence map›Paper›PMID 42212965›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

MiR-940 Suppresses Ferroptosis by Controlling Expression of Key Regulatory Genes.

Andrea Kolak, Juliane Tschuck, Stefanie A I Weiß, Daniel Kaemena, Karolin Klimm, Ana Galhoz, Larissa Ringelstetter, Myles Fennell, Juliane Merl-Pham, Anna Artati and 10 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors.

Andrea KolakCell Signaling and Chemical Biology, Research Unit Signaling and Translation, Helmholtz Zentrum München, Neuherberg, Germany.
Juliane TschuckCell Signaling and Chemical Biology, Research Unit Signaling and Translation, Helmholtz Zentrum München, Neuherberg, Germany.
Stefanie A I WeißCell Signaling and Chemical Biology, Research Unit Signaling and Translation, Helmholtz Zentrum München, Neuherberg, Germany.
Daniel KaemenaInstitute of Virology, Helmholtz Zentrum München, Neuherberg, Germany.
Karolin KlimmCell Signaling and Chemical Biology, Research Unit Signaling and Translation, Helmholtz Zentrum München, Neuherberg, Germany.
Ana GalhozComputational Health Center, Helmholtz Zentrum München, Neuherberg, Germany.
Larissa RingelstetterCell Signaling and Chemical Biology, Research Unit Signaling and Translation, Helmholtz Zentrum München, Neuherberg, Germany.
Myles FennellGene Editing & Screening Core Facility, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Juliane Merl-PhamMetabolomics and Proteomics Core, Helmholtz Zentrum München, Neuherberg, Germany.
Anna ArtatiMetabolomics and Proteomics Core, Helmholtz Zentrum München, Neuherberg, Germany.
Stefanie StrasserCell Signaling and Chemical Biology, Research Unit Signaling and Translation, Helmholtz Zentrum München, Neuherberg, Germany.
Ralph GarippaGene Editing & Screening Core Facility, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Michael WittingMetabolomics and Proteomics Core, Helmholtz Zentrum München, Neuherberg, Germany.ORCID https://orcid.org/0000-0002-1462-4426
Hans ZischkaInstitute of Molecular Toxicology and Pharmacology, Helmholtz Zentrum München, Neuherberg, Germany.
Joel A SchickGenetics and Cellular Engineering Group, Research Unit Signaling and Translation, Helmholtz Zentrum Munich, Neuherberg, Germany.
Stefanie M HauckMetabolomics and Proteomics Core, Helmholtz Zentrum München, Neuherberg, Germany.
Michael P MendenComputational Health Center, Helmholtz Zentrum München, Neuherberg, Germany.
Michelle VincendeauInstitute of Virology, Helmholtz Zentrum München, Neuherberg, Germany.
Brent R StockwellDepartment of Biological Sciences, Columbia University, New York, New York, USA.
Kamyar HadianCell Signaling and Chemical Biology, Research Unit Signaling and Translation, Helmholtz Zentrum München, Neuherberg, Germany.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Tumor Biology and Microenvironment ProgramP30CA013696 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Anil K Rustgi · 1985 to 2026
$115.3M
The Organoid and Cell Culture CoreP30DK132710 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Robert F. Schwabe · 2022 to 2026
$7.2M
High-performance compute cluster for biomedical computingS10OD012351 · OD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CALIFANO, ANDREA · 2012 to 2012
$2.0M
High Performance Computing Cluster for Biomedical ResearchS10OD032433 · OD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CALIFANO, ANDREA · 2023 to 2023
$2.0M
Storage System for High Performance ComputingS10OD021764 · OD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CALIFANO, ANDREA · 2016 to 2016
$600k
BD Biosciences InfluxS10OD020056 · OD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SNOECK, HANS-WILLEM E · 2015 to 2015
$600k
Columbia University Digestive and Liver Disease Research Center 5P30DK132710Deutsche Forschungsgemeinschaft TRR 387/1 - 514894665Molecular Pathology Shared ResourceNational Science Foundation S10OD020056NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA013696NIDDK NIH HHS P30 DK132710NIH HHS S10 OD012351NIH HHS S10 OD020056NIH HHS S10 OD021764NIH HHS S10 OD032433NIH/NCI Cancer Center Support P30CA008748NIH/NCI Cancer Center Support P30CA013696NIH Shared Instrumentation S10OD012351NIH Shared Instrumentation S10OD021764NIH Shared Instrumentation S10OD032433
6 · The paper itself

Abstract

Ferroptosis is a form of regulated cell death that is characterized by iron-dependent lipid peroxidation. This process is regulated by specific metabolites, the lipid composition of the cells, redox-active iron, and antioxidant mechanisms. Although numerous regulators have been identified over the past decade, exploring other mechanisms, particularly from non-coding genomic regions, can build a thorough understanding of the multifaceted regulatory processes underlying ferroptosis. MicroRNAs (miRNAs) play a crucial role in gene regulation and cellular functions. Through a CRISPR KO screen, we identified miR-940 as a negative regulator of ferroptosis. Overexpression of miR-940 in several cell lines consistently suppressed ferroptosis induced by system x

Indexed as

FerroptosisGene Expression RegulationMicroRNAsHumansLipid PeroxidationMicroRNAsferroptosisGPX4lipid peroxidationmicroRNAmiR‐940

Identifiers

PMID42212965
PMCPMC13336029

What OpenQuestion holds

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Read underepoch 390

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.