Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 273

The DOI matches its Crossref record; 10 of the 10 references it cites were found in a registry or an index.

Tumour‐associated microglia/macrophages predict poor prognosis in high‐grade gliomas and correlate with an aggressive tumour subtype

Open access
Sørensen, M. D., Dahlrot, R. H., Boldt, H. B., Hansen, S., Kristensen, B. W.·2018·Neuropathology and Applied Neurobiology

Abstract

Aims: Glioblastomas are highly aggressive and treatment resistant. Increasing evidence suggests that tumour‐associated macrophages/microglia (TAMs) facilitate tumour progression by acquiring a M2‐like phenotype. Our objective was to investigate the prognostic value of TAMs in gliomas using automated quantitative double immunofluorescence. Methods: Samples from 240 patients with primary glioma were stained with antibodies against ionized calcium‐binding adaptor molecule‐1 (IBA‐1) and cluster of differentiation 204 (CD204) to detect TAMs and M2‐like TAMs. The expression levels were quantified by software‐based classifiers. The associations between TAMs, gemistocytic cells and glioblastoma subtype were examined with immuno‐ and haematoxylin–eosin stainings. Three tissue arrays containing glioblastoma specimens were included to study IBA‐1/CD204 levels in central tumour and tumour periphery and to characterize CD204+ cells. Results: Our data revealed that the amount of especially CD204+ TAMs increases with malignancy grade. In grade III–IV, high CD204 expression was associated with shorter survival, while high IBA‐1 intensity correlated with a longer survival. In grade IV, CD204 showed independent prognostic value when adjusting for clinical data and the methylation status of O6‐methylguanine–DNA methyltransferase. Our findings were confirmed in two bioinformatics databases. TAMs were more abundant in central tumour tissue, mesenchymal glioblastomas and gliomas with many gemistocytic cells. CD204+ TAMs co‐expressed proteins related to tumour aggressiveness including matrix metallopeptidase‐14 and hypoxia‐inducible factor‐1α. Conclusions: This is the first study to use automated quantitative immunofluorescence to determine the prognostic impact of TAMs. Our results suggest that M2‐like TAMs hold an unfavourable prognostic value in high‐grade gliomas and may contribute to a pro‐tumourigenic microenvironment.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1111/nan.12428

Cites

10 of 10 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 10 references

Cited by

See all 273

Metadata

Authors
Sørensen, M. D., Dahlrot, R. H., Boldt, H. B., Hansen, S., & Kristensen, B. W.
Venue
Neuropathology and Applied Neurobiology
Publisher
Wiley
Published
2017-09-05
Volume
44
Issue
2
Pages
185-206
ISSN
  • 0305-1846 (ISSN-L)
  • 1365-2990
OpenAlex
W2740090202
Cited by
273
References
10
FWCI
7.76
Type
journal article
Language
en
Open access
hybrid

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: Tumour‐associated microglia/macrophages predict poor prognosis in high‐grade gliomas and correlate with an aggressive tumour subtype. https://app.cochat.ai/papers/10.1111/nan.12428
The paper
Sørensen, M. D., Dahlrot, R. H., Boldt, H. B., Hansen, S., & Kristensen, B. W. (2018). Tumour‐associated microglia/macrophages predict poor prognosis in high‐grade gliomas and correlate with an aggressive tumour subtype. Neuropathology and Applied Neurobiology. https://doi.org/10.1111/nan.12428

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.