Evidence map›Paper›PMID 24056773›Full record

ArticleNature medicine2013

CSF-1R inhibition alters macrophage polarization and blocks glioma progression.

Stephanie M Pyonteck, Leila Akkari, Alberto J Schuhmacher, Robert L Bowman, Lisa Sevenich, Daniela F Quail, Oakley C Olson, Marsha L Quick, Jason T Huse, Virginia Teijeiro and 10 more

Open access · greenAbstract read
In one paragraph

Article in Nature medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1,522 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1,522citing papers in PubMed, 1 pooled it
57.6field-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

1,522 citing papers in PubMed, 1 synthesis or guideline pooled it, 2,418 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  10. TALAVE in Breast Cancer:bioRxiv : the preprint server for biology · 2026
    Article
  11. Review
  12. Next-generation therapeutics for glioblastoma: Challenges and future directions.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Review
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  14. Article
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1,462 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 3 institutions in 1 country.

Stephanie M Pyonteck1] Cancer Biology and Genetics, Memorial Sloan-Kettering Cancer Center (MSKCC), New York, New York, USA. [2].
Leila Akkari
Alberto J Schuhmacher
Robert L Bowman
Lisa Sevenich
Daniela F Quail
Oakley C Olson
Marsha L Quick
Jason T Huse
Virginia Teijeiro
Manu Setty
Christina S Leslie
Yoko Oei
Alicia Pedraza
Jianan Zhang
Cameron W Brennan
James C Sutton
Eric C Holland
Dylan Daniel
Johanna A Joyce
Memorial Sloan Kettering Cancer Center · USNovartis (United States) · USNew York Structural Biology Center · US

Funding

Variability of Cellular Responses to Growth Factors and Drugs During TumorgenesisU54CA148967 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI ALTAN-BONNET, GREGOIRE · 2010 to 2014
$13.8M
Tumor Microenvironment Interactions in Brain TumorsU54CA126518 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI JOYCE, JOHANNA · 2006 to 2010
$6.1M
TRAINING PROGRAM IN MOLECULAR AND CELLULAR BIOLOGYT32GM008539 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI BROWN, ANTHONY M.C. · 1995 to 2020
$5.0M
The Roles of Microglia and Macrophage Populations in the Glioma MicroenvironmentF31CA167863 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI BOWMAN, ROBERT LYLE · 2012 to 2015
$170k
Mechanisms of Macrophage Mediated Chemoprotection in Breast CancerF31CA171384 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI OLSON, OAKLEY C · 2012 to 2015
$170k
NCI NIH HHS CA126518NCI NIH HHS CA148967NCI NIH HHS F31 CA167863NCI NIH HHS F31CA167863NCI NIH HHS F31 CA171384NCI NIH HHS F31CA171384NCI NIH HHS U54 CA126518NCI NIH HHS U54 CA148967NIGMS NIH HHS 5T32GM008539
6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) comprises several molecular subtypes, including proneural GBM. Most therapeutic approaches targeting glioma cells have failed. An alternative strategy is to target cells in the glioma microenvironment, such as tumor-associated macrophages and microglia (TAMs). Macrophages depend on colony stimulating factor-1 (CSF-1) for differentiation and survival. We used an inhibitor of the CSF-1 receptor (CSF-1R) to target TAMs in a mouse proneural GBM model, which significantly increased survival and regressed established tumors. CSF-1R blockade additionally slowed intracranial growth of patient-derived glioma xenografts. Surprisingly, TAMs were not depleted in treated mice. Instead, glioma-secreted factors, including granulocyte-macrophage CSF (GM-CSF) and interferon-γ (IFN-γ), facilitated TAM survival in the context of CSF-1R inhibition. Expression of alternatively activated M2 markers decreased in surviving TAMs, which is consistent with impaired tumor-promoting functions. These gene signatures were associated with enhanced survival in patients with proneural GBM. Our results identify TAMs as a promising therapeutic target for proneural gliomas and establish the translational potential of CSF-1R inhibition for GBM.

Indexed as

AnimalsBrain NeoplasmsDisease ProgressionGlioblastomaMacrophagesMiceReceptor, Macrophage Colony-Stimulating FactorSignal TransductionReceptor, Macrophage Colony-Stimulating Factor

Identifiers

PMID24056773
PMCPMC3840724
OpenAlexW1980485314

What OpenQuestion holds

Textmetadata
LicenceTDM
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.