Evidence map›Paper›PMID 24014382›Full record

ArticleNeuro-oncology2013

Toll-like receptor 2 mediates microglia/brain macrophage MT1-MMP expression and glioma expansion.

Katyayni Vinnakota, Feng Hu, Min-Chi Ku, Petya B Georgieva, Frank Szulzewsky, Andreas Pohlmann, Sonia Waiczies, Helmar Waiczies, Thoralf Niendorf, Seija Lehnardt and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Neuro-oncology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 5% 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

97 citing papers in PubMed, 1 synthesis or guideline pooled it, 143 citations in OpenAlex.

  1. Pooled it
  2. TLR2 and TLR9 in Brain Cancer Patients in Relation to EBV Status.International journal of molecular sciences · 2026
    Article
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  13. Bioinformatics analysis ofTranslational cancer research · 2024
    Article
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  15. Article
  16. Article
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  18. Review
  19. Article
  20. Harnessing innate immune pathways for therapeutic advancement in cancer.Signal transduction and targeted therapy · 2024
    Review

37 more citing papers are in PubMed but not listed here.

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

16 authors at 1 institution in 1 country.

Katyayni VinnakotaCorresponding Author: Prof Dr Helmut Kettenmann, PhD, Cellular Neurosciences, Max Delbrück Center for Molecular Medicine, Robert-Rössle-Str. 10, 13125 Berlin, Germany. kettenmann@mdc-berlin.de.
Feng Hu
Min-Chi Ku
Petya B Georgieva
Frank Szulzewsky
Andreas Pohlmann
Sonia Waiczies
Helmar Waiczies
Thoralf Niendorf
Seija Lehnardt
Uwe-Karsten Hanisch
Michael Synowitz
Darko Markovic
Susanne A Wolf
Rainer Glass
Helmut Kettenmann
Max Delbrück Center · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGlioblastomas are the most aggressive primary brain tumors in humans. Microglia/brain macrophage accumulation in and around the tumor correlates with malignancy and poor clinical prognosis of these tumors. We have previously shown that microglia promote glioma expansion through upregulation of membrane type 1 matrix metalloprotease (MT1-MMP). This upregulation depends on signaling via the Toll-like receptor (TLR) adaptor molecule myeloid differentiation primary response gene 88 (MyD88).

methodsUsing in vitro, ex vivo, and in vivo techniques, we identified TLR2 as the main TLR controlling microglial MT1-MMP expression and promoting microglia-assisted glioma expansion.

resultsThe implantation of mouse GL261 glioma cells into TLR2 knockout mice resulted in significantly smaller tumors, reduced MT1-MMP expression, and enhanced survival rates compared with wild-type control mice. Tumor expansion studied in organotypic brain slices depended on both parenchymal TLR2 expression and the presence of microglia. Glioma-derived soluble factors and synthetic TLR2 specific ligands induced MT1-MMP expression in microglia from wild-type mice, but no such change in MT1-MMP gene expression was observed in microglia from TLR2 knockout mice. We also found evidence that TLR1 and TLR6 cofunction with TLR2 as heterodimers in regulating MT1-MMP expression in vitro.

conclusionsOur results thus show that activation of TLR2 along with TLRs 1 and/or 6 converts microglia into a glioma supportive phenotype.

Indexed as

Macrophage ActivationAnimalsBrainBrain NeoplasmsFemaleGlioblastomaKaplan-Meier EstimateMatrix Metalloproteinase 14MiceMice, Inbred C57BLMice, KnockoutMicrogliaSurvival RateToll-Like Receptor 1Toll-Like Receptor 2Toll-Like Receptor 6Matrix Metalloproteinase 14Toll-Like Receptor 1Toll-Like Receptor 2Toll-Like Receptor 6gliomaglioma-associated microglia/brain macrophagesMT1-MMPTLR

Identifiers

PMID24014382
PMCPMC3813418
OpenAlexW2167548068

What OpenQuestion holds

Textmetadata
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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.