Evidence map›Paper›PMID 30579865›Full record

ArticleEBioMedicine2019

FOXP1 negatively regulates tumor infiltrating lymphocyte migration in human breast cancer.

Pushpamali De Silva, Soizic Garaud, Cinzia Solinas, Alexandre de Wind, Gert Van den Eyden, Vinu Jose, Chunyan Gu-Trantien, Edoardo Migliori, Anaïs Boisson, Céline Naveaux and 5 more

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 13% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

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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

15 authors at 2 institutions in 1 country.

Pushpamali De SilvaMolecular Immunology Unit, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
Soizic GaraudMolecular Immunology Unit, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
Cinzia SolinasMolecular Immunology Unit, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
Alexandre de WindDepartment of Pathology, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
Gert Van den EydenTranslational Cancer Research Unit Antwerp, Oncology Centre, General Hospital Sint Augustinus, Wilrijk, Belgium.
Vinu JoseBreast Cancer Translational Research Laboratory, J-C Heuson, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
Chunyan Gu-TrantienMolecular Immunology Unit, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
Edoardo MiglioriMolecular Immunology Unit, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
Anaïs BoissonMolecular Immunology Unit, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
Céline NaveauxMolecular Immunology Unit, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
Hugues DuvillierFlow Cytometry Core Facility, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
Ligia CraciunDepartment of Pathology, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
Denis LarsimontDepartment of Pathology, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
Martine Piccart-GebhartDepartment of Medicine, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
Karen Willard-GalloMolecular Immunology Unit, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium. Electronic address: karen.willard-gallo@bordet.be.
Université Libre de Bruxelles · BEGZA Ziekenhuizen Campus Sint-Augustinus · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFOXP1, a transcriptional regulator of lymphocyte development, is abnormally expressed in some human tumors. This study investigated FOXP1-mediated regulation of tumor infiltrating lymphocytes (TIL) in untreated primary breast cancer (BC).

methodsFOXP1 expression was analyzed in tissues from primary untreated breast tumors, BC cell lines and the METABRIC gene expression BC dataset. Cytokine and chemokine expression and lymphocyte migration in response to primary tumor supernatants (SN) was compared between FOXP1 FINDING: FOXP1 expression was higher in estrogen receptor positive compared to negative BC. FOXP1

interpretationThese data identify FOXP1 as an important negative regulator of immune responses in BC via its regulation of cytokine and chemokine expression. FUND: Belgian Fund for Scientific Research (FNRS 3.4513.12F) and Opération Télévie (7.4636.13F and 7.4609.15F), Fonds J.C. Heuson and Fonds Lambeau-Marteaux.

Indexed as

Breast NeoplasmsCell MovementCytokinesFemaleForkhead Transcription FactorsGene Expression Regulation, NeoplasticHumansLymphocytes, Tumor-InfiltratingMCF-7 CellsPrognosisReceptors, EstrogenRepressor ProteinsSurvival AnalysisTumor Cells, CulturedUp-RegulationCytokinesForkhead Transcription FactorsFOXP1 protein, humanReceptors, EstrogenRepressor ProteinsBreast cancerChemokinesCytokinesFOXP1Tumor infiltrating lymphocytes

Identifiers

PMID30579865
PMCPMC6354712
OpenAlexW2906638098

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.