Evidence map›Paper›PMID 38566120›Full record

ArticleActa neuropathologica communications2024

Tumor associated microglia/macrophages utilize GPNMB to promote tumor growth and alter immune cell infiltration in glioma.

Fatih Yalcin, Hannah Haneke, Ibrahim E Efe, Leonard D Kuhrt, Edyta Motta, Bernadette Nickl, Charlotte Flüh, Michael Synowitz, Omar Dzaye, Michael Bader and 1 more

Open access · goldAbstract read
In one paragraph

Article in Acta neuropathologica communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

17 citing papers in PubMed, 22 citations in OpenAlex.

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  4. Trem2 exacerbates ischemic brain injury through Gpnmb in a photothrombotic stroke model.Proceedings of the National Academy of Sciences of the United States of America · 2026
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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

11 authors at 4 institutions in 3 countries.

Fatih YalcinMax-Delbrück-Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
Hannah HanekeMax-Delbrück-Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
Ibrahim E EfeMax-Delbrück-Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
Leonard D KuhrtMax-Delbrück-Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
Edyta MottaMax-Delbrück-Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
Bernadette NicklMax-Delbrück-Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
Charlotte FlühDepartment of Neurosurgery, University Medical Center Schleswig-Holstein, Kiel, Germany.
Michael SynowitzDepartment of Neurosurgery, University Medical Center Schleswig-Holstein, Kiel, Germany.
Omar DzayeRussell H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University, Baltimore, MD, USA.
Michael BaderMax-Delbrück-Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
Helmut KettenmannMax-Delbrück-Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany. kettenmann@mdc-berlin.de.ORCID 0000-0001-8208-0291
Max Delbrück Center · DEUniversity Hospital Schleswig-Holstein · DEChinese Academy of Sciences · CNJohns Hopkins University · US

Funding

Einstein Stiftung Berlin EVF-BIH-2016-280-2
6 · The paper itself

Abstract

Tumor-associated microglia and blood-derived macrophages (TAMs) play a central role in modulating the immune suppressive microenvironment in glioma. Here, we show that GPNMB is predominantly expressed by TAMs in human glioblastoma multiforme and the murine RCAS-PDGFb high grade glioma model. Loss of GPNMB in the in vivo tumor microenvironment results in significantly smaller tumor volumes and generates a pro-inflammatory innate and adaptive immune cell microenvironment. The impact of host-derived GPNMB on tumor growth was confirmed in two distinct murine glioma cell lines in organotypic brain slices from GPNMB-KO and control mice. Using published data bases of human glioma, the elevated levels in TAMs could be confirmed and the GPNMB expression correlated with a poorer survival.

Indexed as

Brain NeoplasmsGlioblastomaGliomaAnimalsCell Line, TumorEye ProteinsHumansMacrophagesMembrane GlycoproteinsMiceMicrogliaTumor MicroenvironmentEye ProteinsGPNMB protein, humanGpnmb protein, mouseMembrane GlycoproteinsCD44Experimental gliomaGlioblastomaGPNMBMacrophageMicrogliaMouseRCAS

Identifiers

PMID38566120
PMCPMC10985997
OpenAlexW4393397024

What OpenQuestion holds

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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.