Evidence map›Paper›PMID 37958292›Full record

ArticleCancers2023

The Immunological Landscape of M1 and M2 Macrophages and Their Spatial Distribution in Patients with Malignant Pleural Mesothelioma.

Caddie Laberiano-Fernandez, Camila Machado Baldavira, Juliana Machado-Rugolo, Auriole Tamegnon, Renganayaki Krishna Pandurengan, Alexandre Muxfeldt Ab'Saber, Marcelo Luiz Balancin, Teresa Yae Takagaki, Maria Aparecida Nagai, Vera Luiza Capelozzi and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

7 citing papers in PubMed, 6 citations in OpenAlex.

  1. Trial
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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

11 authors at 2 institutions in 2 countries.

Caddie Laberiano-FernandezDepartment of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0003-4513-6123
Camila Machado BaldaviraDepartment of Pathology, Medical School, University of Sao Paulo, Sao Paulo 01246-903, Brazil.ORCID 0000-0002-5364-7305
Juliana Machado-RugoloDepartment of Pathology, Medical School, University of Sao Paulo, Sao Paulo 01246-903, Brazil.ORCID 0000-0003-3984-4959
Auriole TamegnonDepartment of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Renganayaki Krishna PandurenganDepartment of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Alexandre Muxfeldt Ab'SaberDepartment of Pathology, Medical School, University of Sao Paulo, Sao Paulo 01246-903, Brazil.
Marcelo Luiz BalancinDepartment of Pathology, Medical School, University of Sao Paulo, Sao Paulo 01246-903, Brazil.ORCID 0000-0003-3798-8414
Teresa Yae TakagakiDivision of Pneumology, Instituto do Coração (Incor), Medical School, University of Sao Paulo, Sao Paulo 01246-903, Brazil.ORCID 0000-0003-2277-2100
Maria Aparecida NagaiDepartment of Radiology and Oncology, Medical School, University of Sao Paulo, Sao Paulo 01246-903, Brazil.ORCID 0000-0002-0728-4937
Vera Luiza CapelozziDepartment of Pathology, Medical School, University of Sao Paulo, Sao Paulo 01246-903, Brazil.ORCID 0000-0001-9732-5853
Edwin Roger ParraDepartment of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0001-9068-1636
Universidade de São Paulo · BRThe University of Texas MD Anderson Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSeveral tumor-associated macrophages (TAMs) have shown promise as prognosticators in cancer. Our aim was to validate the importance of TAMs in malignant pleural mesothelioma (MPM) using a two-stage design.

methodsWe explored The Cancer Genome Atlas (TCGA-MESO) to select immune-relevant macrophage genes in MPM, including M1/M2 markers, as a discovery cohort. This computational cohort was used to create a multiplex immunofluorescence panel. Moreover, a cohort of 68 samples of MPM in paraffin blocks was used to validate the macrophage phenotypes and the co-localization and spatial distribution of these immune cells within the TME and the stromal or tumor compartments.

resultsThe discovery cohort revealed six immune-relevant macrophage genes (

conclusionsThe interactions between TAMs in situ and, particularly, CD206

Indexed as

in silico analysismalignant pleural mesotheliomamultiplex immunofluorescenceprognosistranscriptoma

Identifiers

PMID37958292
PMCPMC10650059
OpenAlexW4387904339

What OpenQuestion holds

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LicenceCC BY
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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.