Evidence map›Paper›PMID 32082570›Full record

ArticleClinical & translational immunology2020

CD163

Rodrigo Nalio Ramos, Céline Rodriguez, Margaux Hubert, Maude Ardin, Isabelle Treilleux, Carola H Ries, Emilie Lavergne, Sylvie Chabaud, Amélie Colombe, Olivier Trédan and 8 more

Open access · goldAbstract read
In one paragraph

Article in Clinical & translational immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

53 citing papers in PubMed, 71 citations in OpenAlex.

  1. Review
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  11. Prognostic relevance of CD163Cancer immunology, immunotherapy : CII · 2025
    Article
  12. Article
  13. Review
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  15. Shaping the macrophage landscape in the tumour microenvironment.Central-European journal of immunology · 2025
    Article
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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

18 authors at 6 institutions in 3 countries.

Rodrigo Nalio RamosINSERM U1052 CNRS 5286 Centre Léon Bérard Centre de Recherche en Cancérologie de Lyon Univ Lyon Université Claude Bernard Lyon 1 Lyon France.
Céline RodriguezINSERM U1052 CNRS 5286 Centre Léon Bérard Centre de Recherche en Cancérologie de Lyon Univ Lyon Université Claude Bernard Lyon 1 Lyon France.
Margaux HubertINSERM U1052 CNRS 5286 Centre Léon Bérard Centre de Recherche en Cancérologie de Lyon Univ Lyon Université Claude Bernard Lyon 1 Lyon France.
Maude ArdinINSERM U1052 CNRS 5286 Centre Léon Bérard Centre de Recherche en Cancérologie de Lyon Univ Lyon Université Claude Bernard Lyon 1 Lyon France.
Isabelle TreilleuxCentre Léon Bérard Lyon France.
Carola H RiesRoche Pharmaceutical Research and Early Development Roche Innovation Center Munich Penzberg Germany.
Emilie LavergneCentre Léon Bérard Lyon France.
Sylvie ChabaudCentre Léon Bérard Lyon France.
Amélie ColombeCentre Léon Bérard Lyon France.
Olivier TrédanCentre Léon Bérard Lyon France.
Henrique Gomes GuedesPerola Byington Hospital São Paulo Brazil.
Fábio LaginhaPerola Byington Hospital São Paulo Brazil.ORCID https://orcid.org/0000-0002-7170-6911
Wilfrid RicherInstitut Curie PSL Research University Paris France.
Eliane PiaggioInstitut Curie PSL Research University Paris France.
José Alexandre M BarbutoDepartment of Immunology Institute of Biomedical Sciences - University of São Paulo São Paulo Brazil.
Christophe CauxINSERM U1052 CNRS 5286 Centre Léon Bérard Centre de Recherche en Cancérologie de Lyon Univ Lyon Université Claude Bernard Lyon 1 Lyon France.
Christine Ménétrier-CauxINSERM U1052 CNRS 5286 Centre Léon Bérard Centre de Recherche en Cancérologie de Lyon Univ Lyon Université Claude Bernard Lyon 1 Lyon France.ORCID https://orcid.org/0000-0003-4863-374X
Nathalie Bendriss-VermareINSERM U1052 CNRS 5286 Centre Léon Bérard Centre de Recherche en Cancérologie de Lyon Univ Lyon Université Claude Bernard Lyon 1 Lyon France.ORCID https://orcid.org/0000-0002-8771-3585
Université Claude Bernard Lyon 1 · FRCentre Léon Bérard · FRHospital da Mulher São Paulo · BRInserm · FRRoche Pharma AG (Germany) · DEUniversidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe accumulation of tumor-associated macrophages (TAMs) is correlated with poor clinical outcome, but the mechanisms governing their differentiation from circulating monocytes remain unclear in humans.

methodsUsing multicolor flow cytometry, we evaluated TAMs phenotype in 93 breast cancer (BC) patients. Furthermore, monocytes from healthy donors were cultured in the presence of supernatants from dilacerated primary tumors to investigate their differentiation into macrophages (MΦ)

resultsWe observed that high intra-tumor CD163-expressing TAM density is predictive of reduced survival in BC patients.

conclusionAltogether, our results suggest that systemic factors skew BC patient blood monocytes towards a pro-metastatic profile, resulting in the accumulation of further polarised CD163

Indexed as

breast cancerCD163IFN responsesIL‐10tumor‐associated macrophages

Identifiers

PMID32082570
PMCPMC7017151
OpenAlexW3006205919

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.