Evidence map›Paper›PMID 30651596›Full record

ArticleOncogene2019

ADAM10 mediates malignant pleural mesothelioma invasiveness.

Christelle Sépult, Marine Bellefroid, Natacha Rocks, Kim Donati, Catherine Gérard, Christine Gilles, Andreas Ludwig, Bernard Duysinx, Agnès Noël, Didier Cataldo

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 20 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

10 authors at 2 institutions in 2 countries.

Christelle SépultLaboratory of Tumour and Development Biology, GIGA-cancer, Liège University, Avenue Hippocrate 13, 4000, Liège, Belgium.
Marine BellefroidLaboratory of Tumour and Development Biology, GIGA-cancer, Liège University, Avenue Hippocrate 13, 4000, Liège, Belgium.
Natacha RocksLaboratory of Tumour and Development Biology, GIGA-cancer, Liège University, Avenue Hippocrate 13, 4000, Liège, Belgium.
Kim DonatiLaboratory of Tumour and Development Biology, GIGA-cancer, Liège University, Avenue Hippocrate 13, 4000, Liège, Belgium.
Catherine GérardLaboratory of Tumour and Development Biology, GIGA-cancer, Liège University, Avenue Hippocrate 13, 4000, Liège, Belgium.
Christine GillesLaboratory of Tumour and Development Biology, GIGA-cancer, Liège University, Avenue Hippocrate 13, 4000, Liège, Belgium.
Andreas LudwigInstitute of Pharmacology and Toxicology, RWTH Aachen University, Aachen, Germany.
Bernard DuysinxDepartment of Respiratory diseases, CHU Liège and Liège University, Avenue Hippocrate 13, 4000, Liège, Belgium.
Agnès NoëlLaboratory of Tumour and Development Biology, GIGA-cancer, Liège University, Avenue Hippocrate 13, 4000, Liège, Belgium.
Didier CataldoLaboratory of Tumour and Development Biology, GIGA-cancer, Liège University, Avenue Hippocrate 13, 4000, Liège, Belgium. didier.cataldo@uliege.be.ORCID http://orcid.org/0000-0002-3079-7941
University of Liège · BERWTH Aachen University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malignant pleural mesothelioma (MPM) is an aggressive cancer with limited therapeutic options and treatment efficiency. Even if the latency period between asbestos exposure, the main risk factor, and mesothelioma development is very long, the local invasion of mesothelioma is very rapid leading to a mean survival of one year after diagnosis. ADAM10 (A Disintegrin And Metalloprotease) sheddase targets membrane-bound substrates and its overexpression is associated with progression in several cancers. However, nothing is known about ADAM10 implication in MPM. In this study, we demonstrated higher ADAM10 expression levels in human MPM as compared to control pleural samples and in human MPM cell line. This ADAM10 overexpression was also observed in murine MPM samples. Two mouse mesothelioma cell lines were used in this study including one primary cell line obtained by repeated asbestos fibre injections. We show, in vitro, that ADAM10 targeting through shRNA and pharmacological (GI254023X) approaches reduced drastically mesothelioma cell migration and invasion, as well as for human mesothelioma cells treated with siRNA targeting ADAM10. Moreover, ADAM10 downregulation in murine mesothelioma cells significantly impairs MPM progression in vivo after intrapleural cell injection. We also demonstrate that ADAM10 sheddase downregulation decreases the production of a soluble N-cadherin fragment through membrane N-cadherin, which stimulated mesothelioma cell migration. Taken together, we demonstrate that ADAM10 is overexpressed in MPM and takes part to MPM progression through the generation of N-cadherin fragment that stimulates mesothelioma cell migration. ADAM10 inhibition is worth considering as a therapeutic perspective in mesothelioma context.

Indexed as

ADAM10 ProteinAmyloid Precursor Protein SecretasesAnimalsCadherinsCell Line, TumorCell MovementDisease ProgressionDown-RegulationGene Expression Regulation, NeoplasticHumansLung NeoplasmsMaleMembrane ProteinsMesotheliomaMesothelioma, MalignantMiceADAM10 ProteinADAM10 protein, humanAmyloid Precursor Protein SecretasesCadherinsMembrane Proteins

Identifiers

PMID30651596
PMCPMC6756017
OpenAlexW2909136159

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.