Evidence map›Paper›PMID 31467175›Full record

ArticleBioscience reports2019

ERK1/2 signaling regulates the immune microenvironment and macrophage recruitment in glioblastoma.

Claire Lailler, Christophe Louandre, Mony Chenda Morisse, Thomas Lhossein, Corinne Godin, Marine Lottin, Jean-Marc Constans, Bruno Chauffert, Antoine Galmiche, Zuzana Saidak

Open access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 38 citations in OpenAlex.

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  13. Macrophages/Microglia in the Glioblastoma Tumor Microenvironment.International journal of molecular sciences · 2021
    Review
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  15. Article
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  17. Metabolic reprograming of tumor-associated macrophages.Annals of translational medicine · 2020
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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

10 authors at 2 institutions in 1 country.

Claire LaillerEquipe CHIMERE, EA7516, Université de Picardie Jules Verne, Amiens, France.
Christophe LouandreEquipe CHIMERE, EA7516, Université de Picardie Jules Verne, Amiens, France.
Mony Chenda MorisseEquipe CHIMERE, EA7516, Université de Picardie Jules Verne, Amiens, France.
Thomas LhosseinLaboratoire de Biochimie, Centre de Biologie Humaine, CHU Amiens, France.
Corinne GodinEquipe CHIMERE, EA7516, Université de Picardie Jules Verne, Amiens, France.
Marine LottinService d'Oncologie Médicale, CHU Amiens, France.
Jean-Marc ConstansEquipe CHIMERE, EA7516, Université de Picardie Jules Verne, Amiens, France.
Bruno ChauffertEquipe CHIMERE, EA7516, Université de Picardie Jules Verne, Amiens, France.
Antoine GalmicheEquipe CHIMERE, EA7516, Université de Picardie Jules Verne, Amiens, France.ORCID 0000-0002-5836-4646
Zuzana SaidakEquipe CHIMERE, EA7516, Université de Picardie Jules Verne, Amiens, France Saidak.Zuzana@chu-amiens.fr.ORCID 0000-0003-4629-1141
Chirurgie et extrémité céphalique, caractérisation morphologique et fonctionnelle · FRCentre Hospitalier Universitaire Amiens-Picardie · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tumor microenvironment is an important determinant of glioblastoma (GBM) progression and response to treatment. How oncogenic signaling in GBM cells modulates the composition of the tumor microenvironment and its activation is unclear. We aimed to explore the potential local immunoregulatory function of ERK1/2 signaling in GBM. Using proteomic and transcriptomic data (RNA seq) available for GBM tumors from The Cancer Genome Atlas (TCGA), we show that GBM with high levels of phosphorylated ERK1/2 have increased infiltration of tumor-associated macrophages (TAM) with a non-inflammatory M2 polarization. Using three human GBM cell lines in culture, we confirmed the existence of ERK1/2-dependent regulation of the production of the macrophage chemoattractant CCL2/MCP1. In contrast with this positive regulation of TAM recruitment, we found no evidence of a direct effect of ERK1/2 signaling on two other important aspects of TAM regulation by GBM cells: (1) the expression of the immune checkpoint ligands PD-L1 and PD-L2, expressed at high mRNA levels in GBM compared with other solid tumors; (2) the production of the tumor metabolite lactate recently reported to dampen tumor immunity by interacting with the receptor GPR65 present on the surface of TAM. Taken together, our observations suggest that ERK1/2 signaling regulates the recruitment of TAM in the GBM microenvironment. These findings highlight some potentially important particularities of the immune microenvironment in GBM and could provide an explanation for the recent observation that GBM with activated ERK1/2 signaling may respond better to anti-PD1 therapeutics.

Indexed as

ProteomicsB7-H1 AntigenCell Line, TumorCell MovementCell ProliferationChemokine CCL2Gene Expression Regulation, NeoplasticGlioblastomaHumansMacrophagesMAP Kinase Signaling SystemProgrammed Cell Death 1 Ligand 2 ProteinReceptors, G-Protein-CoupledTranscriptomeTumor MicroenvironmentB7-H1 AntigenCCL2 protein, humanCD274 protein, humanChemokine CCL2GPR65 protein, humanPDCD1LG2 protein, humanProgrammed Cell Death 1 Ligand 2 ProteinReceptors, G-Protein-CoupledCCL2/MCP1ERK1/2GlioblastomaImmune checkpointsThe Cancer Genome AtlasTumour-associated macrophages

Identifiers

PMID31467175
PMCPMC6744584
OpenAlexW2970058039

What OpenQuestion holds

Textmetadata
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.