Evidence map›Paper›PMID 39138571›Full record

ArticleMolecular cancer2024

The CD47/TSP-1 axis: a promising avenue for ovarian cancer treatment and biomarker research.

Aurélie Moniot, Christophe Schneider, Laure Chardin, Elisa Yaniz-Galende, Catherine Genestie, Marion Etiennot, Aubéri Henry, Coralie Drelon, Audrey Le Formal, Benoit Langlois and 16 more

Abstract read
In one paragraph

Article in Molecular cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

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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

26 authors.

Aurélie MoniotApmonia Therapeutics, Reims, France.
Christophe SchneiderUMR 7369 MEDyC, CNRS, Université de Reims Champagne-Ardenne, Reims, France.
Laure ChardinGustave-Roussy Cancer Campus Université Paris-Saclay GINECO/GINEGEPS, Inserm U981, Villejuif, France.
Elisa Yaniz-GalendeGustave-Roussy Cancer Campus Université Paris-Saclay GINECO/GINEGEPS, Inserm U981, Villejuif, France.
Catherine GenestieGustave-Roussy Cancer Campus Université Paris-Saclay GINECO/GINEGEPS, Inserm U981, Villejuif, France.
Marion EtiennotApmonia Therapeutics, Reims, France.
Aubéri HenryApmonia Therapeutics, Reims, France.
Coralie DrelonUMR 7369 MEDyC, CNRS, Université de Reims Champagne-Ardenne, Reims, France.
Audrey Le FormalGustave-Roussy Cancer Campus Université Paris-Saclay GINECO/GINEGEPS, Inserm U981, Villejuif, France.
Benoit LangloisUMR 7369 MEDyC, CNRS, Université de Reims Champagne-Ardenne, Reims, France.
Laurence VenatCentre Hospitalier Universitaire Dupuytren, Limoges, France.
Christophe LouvetInstitut Mutualiste Montsouris-Jourdan, Paris, France.
Laure FavierCentre Georges-François Leclerc, Dijon, France.
Alain LortholaryHôpital Privé du Confluent - GINECO, Nantes, France.
Dominique Berton-RigaudICO Centre René Gauducheau - GINECO, Saint-Herblain, France.
Nadine DohollouPolyclinique Bordeaux Nord, Bordeaux, France.
Christophe DesauwCentre Hospitalier Régional Universitaire de Lille, Hôpital Huriez, Lille, France.
Michel FabbroICM Val d'Aurelle - GINECO, Montpellier, France.
Emmanuelle MalaurieCentre Hospitalier Intercommunal de Créteil, Créteil, France.
Coraline DubotInstitut Curie - Hôpital René Huguenin - GINECO, Saint-Cloud, France.
Jean Emmanuel KurtzHôpitaux Universitaires de Strasbourg, Strasbourg, France.
Nathalie Bonichon LamichhaneClinique Tivoli-Ducos, Bordeaux, France.
Éric Pujade-LauraineARCAGY-GINECO, Paris, France.
Albin JeanneApmonia Therapeutics, Reims, France.
Alexandra Leary *Gustave-Roussy Cancer Campus Université Paris-Saclay GINECO/GINEGEPS, Inserm U981, Villejuif, France.
Stéphane Dedieu *UMR 7369 MEDyC, CNRS, Université de Reims Champagne-Ardenne, Reims, France. stephane.dedieu@univ-reims.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOvarian cancer (OC) remains one of the most challenging and deadly malignancies facing women today. While PARP inhibitors (PARPis) have transformed the treatment landscape for women with advanced OC, many patients will relapse and the PARPi-resistant setting is an area of unmet medical need. Traditional immunotherapies targeting PD-1/PD-L1 have failed to show any benefit in OC. The CD47/TSP-1 axis may be relevant in OC. We aimed to describe changes in CD47 expression with platinum therapy and their relationship with immune features and prognosis.

methodsTumor and blood samples collected from OC patients in the CHIVA trial were assessed for CD47 and TSP-1 before and after neoadjuvant chemotherapy (NACT) and multiplex analysis was used to investigate immune markers. Considering the therapeutic relevance of targeting the CD47/TSP-1 axis, we used the CD47-derived TAX2 peptide to selectively antagonize it in a preclinical model of aggressive ovarian carcinoma.

resultsSignificant reductions in CD47 expression were observed post NACT. Tumor patients having the highest CD47 expression profile at baseline showed the greatest CD4

conclusionsOur study thus (1) proposes a CD47-based stratification of patients who may be most likely to benefit from postoperative immunotherapy, and (2) suggests that TAX2 is a potential alternative therapy for patients relapsing on PARP inhibitors.

Indexed as

Biomarkers, TumorCD47 AntigenOvarian NeoplasmsThrombospondin 1AnimalsCell Line, TumorFemaleGene Expression Regulation, NeoplasticHumansMiceMiddle AgedNeoadjuvant TherapyPrognosisXenograft Model Antitumor AssaysBiomarkers, TumorCD47 AntigenCD47 protein, humanThrombospondin 1thrombospondin-1, humanCD47Neoadjuvant chemotherapyOvarian cancerPARPTSP-1

Identifiers

PMID39138571
PMCPMC11323699

What Socratic holds

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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 Socratic graph.