Evidence map›Paper›PMID 29563634›Full record

ArticleBritish journal of cancer2018

The tyrosine-kinase inhibitor sunitinib targets vascular endothelial (VE)-cadherin: a marker of response to antitumoural treatment in metastatic renal cell carcinoma.

Helena Polena, Julie Creuzet, Maeva Dufies, Adama Sidibé, Abir Khalil-Mgharbel, Aude Salomon, Alban Deroux, Jean-Louis Quesada, Caroline Roelants, Odile Filhol and 9 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

17 citing papers in PubMed, 31 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

19 authors at 8 institutions in 2 countries.

Helena PolenaUniv-Grenoble Alpes, INSERM, CNRS, BIG-BCI Biology of Cancer and Infection, Grenoble, F- 38054, France.
Julie CreuzetUniv-Grenoble Alpes, INSERM, CNRS, BIG-BCI Biology of Cancer and Infection, Grenoble, F- 38054, France.
Maeva DufiesBiomedical Department, Centre Scientifique de Monaco, Monaco, Monaco.
Adama SidibéUniv-Grenoble Alpes, INSERM, CNRS, BIG-BCI Biology of Cancer and Infection, Grenoble, F- 38054, France.
Abir Khalil-MgharbelUniv-Grenoble Alpes, INSERM, CNRS, BIG-BCI Biology of Cancer and Infection, Grenoble, F- 38054, France.
Aude SalomonUniv-Grenoble Alpes, INSERM, CNRS, BIG-BCI Biology of Cancer and Infection, Grenoble, F- 38054, France.
Alban DerouxGrenoble University Hospital, Division of Internal Medicine, Grenoble, F-38043, France.
Jean-Louis QuesadaINSERM, Unité 003, Clinical Investigation Center, Grenoble University Hospital, Grenoble, F-38043, France.
Caroline RoelantsUniv-Grenoble Alpes, INSERM, CNRS, BIG-BCI Biology of Cancer and Infection, Grenoble, F- 38054, France.
Odile FilholUniv-Grenoble Alpes, INSERM, CNRS, BIG-BCI Biology of Cancer and Infection, Grenoble, F- 38054, France.
Claude CochetUniv-Grenoble Alpes, INSERM, CNRS, BIG-BCI Biology of Cancer and Infection, Grenoble, F- 38054, France.
Ellen BlancUnicancer, Centre de Lutte contre Le Cancer Léon Bérard, Lyon, F-69008, France.
Céline Ferlay-SeguraUnicancer, Centre de Lutte contre Le Cancer Léon Bérard, Lyon, F-69008, France.
Delphine BorchielliniDepartment of Clinical Research, Innovation and Statistics, Centre Antoine Lacassagne, Nice, F-06000, France.
Jean-Marc FerreroDepartment of Clinical Research, Innovation and Statistics, Centre Antoine Lacassagne, Nice, F-06000, France.
Bernard EscudierGustave Roussy Cancer Campus, Grand Paris, Villejuif, F-94800, France.
Sylvie NégrierUnicancer, Centre de Lutte contre Le Cancer Léon Bérard, Lyon, F-69008, France.
Gilles PagesUniversity of Nice Sophia Antipolis, Institute for Research on Cancer and Aging of Nice, CNRS UMR 7284, INSERM U1081, Centre Antoine Lacassagne, Nice, F-06107, France.
Isabelle VilgrainUniv-Grenoble Alpes, INSERM, CNRS, BIG-BCI Biology of Cancer and Infection, Grenoble, F- 38054, France. ivilgrain@cea.fr.
Inserm · FRCentre Antoine Lacassagne · FRCentre Léon Bérard · FRUniversité Grenoble Alpes · FRCentre National de la Recherche Scientifique · FRUnit of Virus Host Cell Interactions · FRInstitut Gustave Roussy · FRScientific Centre of Monaco · MC

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVascular endothelial (VE)-cadherin is an endothelial cell-specific protein responsible for endothelium integrity. Its adhesive properties are regulated by post-translational processing, such as tyrosine phosphorylation at site Y

methodsThe effects of kidney cancer biotherapies were tested on an endothelial monolayer model mimicking the endothelium lining blood vessels and on a homotypic and heterotypic 3D cell model mimicking tumour growth. sVE was quantified by ELISA in renal cell carcinoma patients initiating sunitinib (48 patients) or bevacizumab (83 patients) in the first-line metastatic setting (SUVEGIL and TORAVA trials).

resultsHuman VE-cadherin is a direct target for sunitinib which inhibits its VEGF-induced phosphorylation and cleavage on endothelial monolayer and endothelial cell migration in the 3D model. The tumour cell environment modulates VE-cadherin functions through MMPs and VEGF. We demonstrate the presence of soluble VE-cadherin in the sera of mRCC patients (n = 131) which level at baseline, is higher than in a healthy donor group (n = 96). Analysis of sVE level after 4 weeks of treatment showed that a decrease in sVE level discriminates the responders vs. non-responders to sunitinib, but not bevacizumab.

conclusionsThese data highlight the interest for the sVE bioassay in future follow-up of cancer patients treated with targeted therapies such as tyrosine-kinase inhibitors.

Indexed as

Biomarkers, PharmacologicalAntineoplastic AgentsBiomarkers, TumorCadherinsCarcinoma, Renal CellCells, CulturedClinical Trials as TopicEndothelium, VascularHumansHuman Umbilical Vein Endothelial CellsKidney NeoplasmsMolecular Targeted TherapyNeoplasm MetastasisRetrospective StudiesSunitinibTreatment OutcomeAntineoplastic AgentsBiomarkers, PharmacologicalBiomarkers, TumorCadherinsSunitinib

Identifiers

PMID29563634
PMCPMC5943344
OpenAlexW2792240357

What OpenQuestion 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 OpenQuestion graph.