Evidence map›Paper›PMID 36194288›Full record

ArticleCancer immunology, immunotherapy : CII2023

Detecting monocyte trafficking in an animal model of glioblastoma using R

Runze Yang, A Max Hamilton, Hongfu Sun, Khalil S Rawji, Susobhan Sarkar, Reza Mirzaei, G Bruce Pike, V Wee Yong, Jeff F Dunn

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2023. 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
0.2field-weighted citation impact, top 53% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Review
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

9 authors at 2 institutions in 2 countries.

Runze YangDepartment of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Canada.ORCID http://orcid.org/0000-0002-1192-9363
A Max HamiltonCumming School of Medicine, Hotchkiss Brain Institute, University of Calgary, Calgary, Canada.
Hongfu SunCumming School of Medicine, Hotchkiss Brain Institute, University of Calgary, Calgary, Canada.
Khalil S RawjiCumming School of Medicine, Hotchkiss Brain Institute, University of Calgary, Calgary, Canada.
Susobhan SarkarCumming School of Medicine, Hotchkiss Brain Institute, University of Calgary, Calgary, Canada.
Reza MirzaeiCumming School of Medicine, Hotchkiss Brain Institute, University of Calgary, Calgary, Canada.
G Bruce PikeDepartment of Radiology, Cumming School of Medicine, University of Calgary, N.W. Calgary, 3330 Hospital Drive, Calgary, AB, T2N 4N1, Canada.
V Wee YongCumming School of Medicine, Hotchkiss Brain Institute, University of Calgary, Calgary, Canada.
Jeff F DunnDepartment of Radiology, Cumming School of Medicine, University of Calgary, N.W. Calgary, 3330 Hospital Drive, Calgary, AB, T2N 4N1, Canada. dunnj@ucalgary.ca.
University of Calgary · CAQueensland University of Technology · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe role of tumor-associated macrophages (TAMs) in glioblastoma (GBM) disease progression has received increasing attention. Recent advances have shown that TAMs can be re-programmed to exert a pro-inflammatory, anti-tumor effect to control GBMs. However, imaging methods capable of differentiating tumor progression from immunotherapy treatment effects have been lacking, making timely assessment of treatment response difficult. We showed that tracking monocytes using iron oxide nanoparticle (USPIO) with MRI can be a sensitive imaging method to detect therapy response directed at the innate immune system.

methodsWe implanted syngeneic mouse glioma stem cells into C57/BL6 mice and treated the animals with either niacin (a stimulator of innate immunity) or vehicle. Animals were imaged using an anatomical MRI sequence, R

resultsCompared to vehicles, niacin-treated animals showed significantly higher susceptibility and R

conclusionMRI with USPIO injection can detect therapeutic responses of innate immune stimulating agents before changes in tumor size have occurred, providing a potential complementary imaging technique to monitor cancer immunotherapies. MANUSCRIPT HIGHLIGHT: We show that iron oxide nanoparticles (USPIOs) can be used to label innate immune cells and detect the trafficking of pro-inflammatory monocytes into the glioblastoma. This preceded changes in tumor size, making it a more sensitive imaging technique.

Indexed as

GlioblastomaGliomaNiacinAnimalsMagnetic Resonance ImagingMiceModels, AnimalMonocytesNiacinCell trackingGlioblastomaImmunotherapyIron oxideMRI

Identifiers

PMID36194288
PMCPMC10992300
OpenAlexW4300972003

What OpenQuestion holds

Textmetadata
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.