Evidence map›Paper›PMID 41943844›Full record

ArticleInternational journal of biological sciences2026

IGF2BP2 Deficiency in Macrophages Impairs Migration, Reprograms Metabolism, and Limits Tumor Progression.

Hanna S Schymik, Selina Wrublewsky, Marcus Höring, Gerhard Liebisch, Simon Both, Gilles Gasparoni, Caroline Bickelmann, Hanah Robertson, Charlotte Dahlem, Jörn Walter and 5 more

Abstract read
In one paragraph

Article in International journal of biological sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

15 authors.

Hanna S SchymikDepartment of Pharmacy, Pharmaceutical Biology, Saarland University, Saarbrücken, Germany.
Selina WrublewskyInstitute for Clinical & Experimental Surgery, Saarland University, Homburg, Germany.
Marcus HöringInstitute of Clinical Chemistry and Laboratory Medicine, University Hospital Regensburg, Regensburg, Germany.
Gerhard LiebischInstitute of Clinical Chemistry and Laboratory Medicine, University Hospital Regensburg, Regensburg, Germany.
Simon BothDepartment of Pharmacy, Pharmaceutical Biology, Saarland University, Saarbrücken, Germany.
Gilles GasparoniDepartment of Genetics/Epigenetics, Saarland University, Saarbrücken, Germany.
Caroline BickelmannInstitute for Clinical & Experimental Surgery, Saarland University, Homburg, Germany.
Hanah RobertsonCenter for Bioinformatics, Saarland University, Saarbrücken. Germany.
Charlotte DahlemDepartment of Pharmacy, Pharmaceutical Biology, Saarland University, Saarbrücken, Germany.
Jörn WalterDepartment of Genetics/Epigenetics, Saarland University, Saarbrücken, Germany.
Volkhard HelmsCenter for Bioinformatics, Saarland University, Saarbrücken. Germany.
Matthias W LaschkeInstitute for Clinical & Experimental Surgery, Saarland University, Homburg, Germany.
Emmanuel AmpofoInstitute for Clinical & Experimental Surgery, Saarland University, Homburg, Germany.
Jessica HoppstädterDepartment of Pharmacy, Pharmaceutical Biology, Saarland University, Saarbrücken, Germany.
Alexandra K KiemerDepartment of Pharmacy, Pharmaceutical Biology, Saarland University, Saarbrücken, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While insulin-like growth factor 2 mRNA-binding protein 2 (IGF2BP2) has been extensively studied in tumor cells, its role in immune cells within the tumor microenvironment, particularly in macrophages, remains largely unknown. Here, we reveal a critical function of IGF2BP2 in macrophages, demonstrating that myeloid-specific deletion of IGF2BP2 profoundly alters macrophage metabolism and polarization, and markedly impairs tumor progression. Bulk RNA sequencing of IGF2BP2 knockout (KO) macrophages revealed significant alterations in gene expression profiles, particularly impacting pathways associated with glycolysis, mitochondrial function, cell motility, and cell migration. Functional assays confirmed increased glycolytic activity and a concomitant reduction in maximal respiration and reserve respiratory capacity, indicating a metabolic shift towards glycolysis. Furthermore, IGF2BP2 deficiency impaired tumor-associated macrophage (TAM)-like polarization

Indexed as

MacrophagesRNA-Binding ProteinsAnimalsCell MovementGlycolysisMetabolic ReprogrammingMiceMice, KnockoutTumor-Associated MacrophagesTumor MicroenvironmentIGF2BP2 protein, mouseRNA-Binding Proteins

Identifiers

PMID41943844
PMCPMC13050439

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.