Evidence map›Paper›PMID 31354732›Full record

ArticleFrontiers in immunology2019

A Bispecific Antibody-Based Approach for Targeting Mesothelin in Triple Negative Breast Cancer.

Joanie Del Bano, Rémy Florès-Florès, Emmanuelle Josselin, Armelle Goubard, Laetitia Ganier, Rémy Castellano, Patrick Chames, Daniel Baty, Brigitte Kerfelec

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

39 citing papers in PubMed, 76 citations in OpenAlex.

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  8. Harnessing the potential of CD40 agonism in cancer therapy.Cytokine & growth factor reviews · 2024
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  15. Frontiers in immunology · 2023
    Review
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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

9 authors at 5 institutions in 1 country.

Joanie Del BanoAix Marseille Univ, CNRS, INSERM, Institut Paoli-Calmette, CRCM, Marseille, France.
Rémy Florès-FlorèsAix Marseille Univ, CNRS, Institut de Biologie du Développement de Marseille, UMR7288, Marseille, France.
Emmanuelle JosselinAix Marseille Univ, CNRS, INSERM, Institut Paoli-Calmette, CRCM, Marseille, France.
Armelle GoubardAix Marseille Univ, CNRS, INSERM, Institut Paoli-Calmette, CRCM, Marseille, France.
Laetitia GanierAix Marseille Univ, CNRS, INSERM, Institut Paoli-Calmette, CRCM, Marseille, France.
Rémy CastellanoAix Marseille Univ, CNRS, INSERM, Institut Paoli-Calmette, CRCM, Marseille, France.
Patrick ChamesAix Marseille Univ, CNRS, INSERM, Institut Paoli-Calmette, CRCM, Marseille, France.
Daniel BatyAix Marseille Univ, CNRS, INSERM, Institut Paoli-Calmette, CRCM, Marseille, France.
Brigitte KerfelecAix Marseille Univ, CNRS, INSERM, Institut Paoli-Calmette, CRCM, Marseille, France.
Inserm · FRCentre National de la Recherche Scientifique · FRInstitut Paoli-Calmettes · FRCentre de Recherche en Cancérologie de Marseille · FRInstitut Pprime · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Triple negative breast cancers (TNBC) remain a major medical challenge due to poor prognosis and limited treatment options. Mesothelin is a glycosyl-phosphatidyl inositol-linked membrane protein with restricted normal expression and high level expression in a large proportion of TNBC, thus qualifying as an attractive target. Its overexpression in breast tumors has been recently correlated with a decreased disease-free survival and an increase of distant metastases. The objective of the study was to investigate the relevance of a bispecific antibody-based immunotherapy approach through mesothelin targeting and CD16 engagement using a Fab-like bispecific format (MesobsFab). Using two TNBC cell lines with different level of surface mesothelin and epithelial/mesenchymal phenotypes, we showed that,

Indexed as

Antibodies, BispecificAntibody-Dependent Cell CytotoxicityBreast NeoplasmsCell Line, TumorEpitopesFemaleGPI-Linked ProteinsHumansImmunotherapyKiller Cells, NaturalMesothelinReceptors, IgGTriple Negative Breast NeoplasmsAntibodies, BispecificEpitopesGPI-Linked ProteinsMesothelinMSLN protein, humanReceptors, IgGbispecific antibody (bsAb)immunotherapymesothelin (MSLN)multicellular tumor spheroid model (MCTS)natural killer cellstriple negative breast cancer (TNBC)

Identifiers

PMID31354732
PMCPMC6636429
OpenAlexW2962536070

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.