Evidence map›Paper›PMID 26539644›Full record

ArticleOncotarget2015

Sensitivity of human pleural mesothelioma to oncolytic measles virus depends on defects of the type I interferon response.

Carole Achard, Nicolas Boisgerault, Tiphaine Delaunay, David Roulois, Steven Nedellec, Pierre-Joseph Royer, Mallory Pain, Chantal Combredet, Mariana Mesel-Lemoine, Laurent Cellerin and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

28 citing papers in PubMed, 46 citations in OpenAlex.

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  17. Type 1 Interferon Responses Underlie Tumor-Selective Replication of Oncolytic Measles Virus.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
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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

14 authors at 7 institutions in 1 country.

Carole AchardINSERM, UMR892, Institut de Recherche en Santé de l'Université de Nantes, Nantes, France.
Nicolas BoisgeraultINSERM, UMR892, Institut de Recherche en Santé de l'Université de Nantes, Nantes, France.
Tiphaine DelaunayINSERM, UMR892, Institut de Recherche en Santé de l'Université de Nantes, Nantes, France.
David RouloisINSERM, UMR892, Institut de Recherche en Santé de l'Université de Nantes, Nantes, France.
Steven NedellecUniversité de Nantes, Nantes, France.
Pierre-Joseph RoyerUniversité de Nantes, Nantes, France.
Mallory PainUniversité de Nantes, Nantes, France.
Chantal CombredetCNRS UMR3569, Unité de Génomique Virale et Vaccination, Institut Pasteur, Paris, France.
Mariana Mesel-LemoineCNRS UMR3569, Unité de Génomique Virale et Vaccination, Institut Pasteur, Paris, France.
Laurent CellerinCHU de Nantes, Service d'Oncologie Médicale Thoracique et Digestive, Nantes, France.
Antoine MagnanUniversité de Nantes, Nantes, France.
Frédéric TangyCNRS UMR3569, Unité de Génomique Virale et Vaccination, Institut Pasteur, Paris, France.
Marc GrégoireINSERM, UMR892, Institut de Recherche en Santé de l'Université de Nantes, Nantes, France.
Jean-François FonteneauINSERM, UMR892, Institut de Recherche en Santé de l'Université de Nantes, Nantes, France.
Inserm · FRNantes Université · FRInstitut Pasteur · FRCentre Hospitalier Universitaire de Nantes · FRCentre National de la Recherche Scientifique · FRInstitut du Thorax · FRStructure Fédérative de Recherche Bonamy

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Attenuated measles virus (MV) is currently being evaluated as an oncolytic virus in clinical trials and could represent a new therapeutic approach for malignant pleural mesothelioma (MPM). Herein, we screened the sensitivity to MV infection and replication of twenty-two human MPM cell lines and some healthy primary cells. We show that MV replicates in fifteen of the twenty-two MPM cell lines. Despite overexpression of CD46 by a majority of MPM cell lines compared to healthy cells, we found that the sensitivity to MV replication did not correlate with this overexpression. We then evaluated the antiviral type I interferon (IFN) responses of MPM cell lines and healthy cells. We found that healthy cells and the seven insensitive MPM cell lines developed a type I IFN response in presence of the virus, thereby inhibiting replication. In contrast, eleven of the fifteen sensitive MPM cell lines were unable to develop a complete type I IFN response in presence of MV. Finally, we show that addition of type I IFN onto MV sensitive tumor cell lines inhibits replication. These results demonstrate that defects in type I IFN response are frequent in MPM and that MV takes advantage of these defects to exert oncolytic activity.

Indexed as

Virus ReplicationAntigens, CDCell Adhesion MoleculesCell Line, TumorHost-Pathogen InteractionsHumansInterferon Type IMeasles virusMembrane Cofactor ProteinMesotheliomaNectinsOncolytic VirotherapyOncolytic VirusesPleural NeoplasmsReceptors, Cell SurfaceSignaling Lymphocytic Activation Molecule Family Member 1Antigens, CDCD46 protein, humanCell Adhesion MoleculesInterferon Type IMembrane Cofactor ProteinNECTIN4 protein, humanNectinsReceptors, Cell SurfaceSignaling Lymphocytic Activation Molecule Family Member 1measles virusmesotheliomaoncolytic virotherapyoncolytic virustype I interferon

Identifiers

PMID26539644
PMCPMC4792599
OpenAlexW2139023340

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.