Evidence map›Paper›PMID 39516530›Full record

ArticleCommunications biology2024

ZBTB18 regulates cytokine expression and affects microglia/macrophage recruitment and commitment in glioblastoma.

Roberto Ferrarese, Kevin Joseph, Geoffroy Andrieux, Ira Verena Haase, Francesca Zanon, Eva Kling, Annalisa Izzo, Eyleen Corrales, Marius Schwabenland, Marco Prinz and 4 more

Abstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

14 authors.

Roberto Ferrarese *Department of Neurosurgery, Medical Center-University of Freiburg, Freiburg, Germany.
Kevin Joseph *Department of Neurosurgery, Medical Center-University of Freiburg, Freiburg, Germany.ORCID 0000-0001-6317-8736
Geoffroy Andrieux *Institute of Medical Bioinformatics and Systems Medicine, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID 0000-0002-5389-9481
Ira Verena HaaseDepartment of Neurosurgery, Medical Center-University of Freiburg, Freiburg, Germany.
Francesca ZanonDepartment of Neurosurgery, Medical Center-University of Freiburg, Freiburg, Germany.
Eva KlingDepartment of Neurosurgery, Medical Center-University of Freiburg, Freiburg, Germany.
Annalisa IzzoDepartment of Neurosurgery, Medical Center-University of Freiburg, Freiburg, Germany.ORCID 0000-0001-5826-7945
Eyleen CorralesInstitute of Medical Bioinformatics and Systems Medicine, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID 0000-0002-4767-1640
Marius SchwabenlandInstitute of Neuropathology, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID 0000-0003-2205-5427
Marco PrinzInstitute of Neuropathology, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID 0000-0002-0349-1955
Vidhya Madapusi RaviDepartment of Neurosurgery, Medical Center-University of Freiburg, Freiburg, Germany.ORCID 0000-0003-0062-2099
Melanie BoerriesInstitute of Medical Bioinformatics and Systems Medicine, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID 0000-0002-3670-0602
Dieter Henrik HeilandDepartment of Neurosurgery, Medical Center-University of Freiburg, Freiburg, Germany.ORCID 0000-0002-9258-3033
Maria Stella CarroDepartment of Neurosurgery, Medical Center-University of Freiburg, Freiburg, Germany. mariastella.carro@uninsubria.it.ORCID 0000-0002-8570-7691

Funding

Deutsche Krebshilfe (German Cancer Aid) 70113120
6 · The paper itself

Abstract

Glioma associated macrophages/microglia (GAMs) play an important role in glioblastoma (GBM) progression, due to their massive recruitment to the tumor site and polarization to a tumor promoting phenotype. GAMs secrete a variety of cytokines, which facilitate tumor cell growth and invasion, and prevent other immune cells from mounting an immune response against the tumor. Here, we demonstrate that zinc finger and BTB containing domain 18 (ZBTB18), a transcriptional repressor with tumor suppressive function in glioblastoma, impairs the production of key cytokines, which function as chemoattractant for GAMs. Consistently, we observe a reduced migration of GAMs when ZBTB18 is expressed by glioblastoma cells, both in cell culture and in vivo experiments. Moreover, RNA sequencing analysis shows that the presence of ZBTB18 in glioblastoma cells alters the commitment of conditioned microglia, suggesting the loss of the immune-suppressive phenotype and the acquisition of pro-inflammatory features. Thus, therapeutic approaches to increase ZBTB18 expression in GBM cells could represent an effective adjuvant to immune therapy in GBM.

Indexed as

CytokinesGlioblastomaMicrogliaRepressor ProteinsAnimalsBrain NeoplasmsCell Line, TumorCell MovementGene Expression Regulation, NeoplasticHumansMacrophagesMiceCytokinesRepressor ProteinsZBTB18 protein, human

Identifiers

PMID39516530
PMCPMC11549471

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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.