Evidence map›Paper›PMID 26066800›Full record

ArticlePloS one2015

CSF1R Protein Expression in Reactive Lymphoid Tissues and Lymphoma: Its Relevance in Classical Hodgkin Lymphoma.

Ana M Martín-Moreno, Giovanna Roncador, Lorena Maestre, Elena Mata, Scherezade Jiménez, Jorge L Martínez-Torrecuadrada, Ana I Reyes-García, Carmen Rubio, José F Tomás, Mónica Estévez and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 16% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
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  15. Colony-Stimulating Factor 1 Receptor (CSF1R) Activates AKT/mTOR Signaling and Promotes T-Cell Lymphoma Viability.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
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  20. PD-1, FOXP3, and CSF-1R expression in patients with Hodgkin lymphoma and their prognostic value.International journal of clinical and experimental pathology · 2018
    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

13 authors at 4 institutions in 2 countries.

Ana M Martín-MorenoPathology Department, MD Anderson Cancer Center, Madrid, Spain.
Giovanna RoncadorMonoclonal Antibodies Unit, Spanish National Cancer Centre (CNIO), Madrid, Spain.
Lorena MaestreMonoclonal Antibodies Unit, Spanish National Cancer Centre (CNIO), Madrid, Spain.
Elena MataPathology Department, MD Anderson Cancer Center, Madrid, Spain.
Scherezade JiménezMonoclonal Antibodies Unit, Spanish National Cancer Centre (CNIO), Madrid, Spain.
Jorge L Martínez-TorrecuadradaProteomics Unit, Spanish National Cancer Centre (CNIO), Madrid, Spain.
Ana I Reyes-GarcíaMonoclonal Antibodies Unit, Spanish National Cancer Centre (CNIO), Madrid, Spain.
Carmen RubioPathology Department, MD Anderson Cancer Center, Madrid, Spain.
José F TomásHaematology Department, MD Anderson Cancer Center, Madrid, Spain.
Mónica EstévezHaematology Department, MD Anderson Cancer Center, Madrid, Spain.
Karen PulfordNuffield Division of Clinical Laboratory Sciences, Radcliffe Department of Medicine, University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom.
Miguel A PirisPathology Department, Hospital Universitario Marqués de Valdecilla, Santander, Spain.
Juan F GarcíaPathology Department, MD Anderson Cancer Center, Madrid, Spain.
MD Anderson Cancer Center Madrid · ESSpanish National Cancer Research Centre · ESMarqués de Valdecilla University Hospital · ESUniversity of Oxford · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumour-associated macrophages (TAMs) have been associated with survival in classic Hodgkin lymphoma (cHL) and other lymphoma types. The maturation and differentiation of tissue macrophages depends upon interactions between colony-stimulating factor 1 receptor (CSF1R) and its ligands. There remains, however, a lack of consistent information on CSF1R expression in TAMs. A new monoclonal antibody, FER216, was generated to investigate CSF1R protein distribution in formalin fixed tissue samples from 24 reactive lymphoid tissues and 187 different lymphoma types. We also analysed the distribution of CSF1R+, CD68+ and CD163+ macrophages by double immunostaining, and studied the relationship between CSF1R expression and survival in an independent series of 249 cHL patients. CSF1R+ TAMs were less frequent in B-cell lymphocytic leukaemia and lymphoblastic B-cell lymphoma than in diffuse large B-cell lymphoma, peripheral T-cell lymphoma, angioimmunoblastic T-cell lymphoma and cHL. HRS cells in cHL and, with the exception of three cases of anaplastic large cell lymphoma, the neoplastic cells in NHLs, lacked detectable CSF1R protein. A CSF1R+ enriched microenvironment in cHL was associated with shorter survival in an independent series of 249 cHL patients. CSF1R pathway activation was evident in the cHL and inactivation of this pathway could be a potential therapeutic target in cHL cases.

Indexed as

AnimalsCell Line, TumorGene ExpressionHodgkin DiseaseHumansImmunohistochemistryImmunoprecipitationLymphoid TissueLymphomaMiceReceptor, Macrophage Colony-Stimulating FactorSignal TransductionReceptor, Macrophage Colony-Stimulating Factor

Identifiers

PMID26066800
PMCPMC4466308
OpenAlexW1493858955

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.