Evidence map›Paper›PMID 36810959›Full record

ArticleMolecular oncology2023

A group of novel VEGF splice variants as alternative therapeutic targets in renal cell carcinoma.

Christopher Montemagno, Jérôme Durivault, Cécile Gastaldi, Maeva Dufies, Valérie Vial, Xingkang He, Damien Ambrosetti, Anna Kamenskaya, Sylvie Negrier, Jean-Christophe Bernhard and 3 more

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
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  5. Review
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

13 authors at 7 institutions in 3 countries.

Christopher MontemagnoBiomedical Department, Centre Scientifique de Monaco, Monaco.
Jérôme DurivaultBiomedical Department, Centre Scientifique de Monaco, Monaco.
Cécile GastaldiLIA BAHN, CSM-UVSQ, Monaco, Monaco.
Maeva DufiesBiomedical Department, Centre Scientifique de Monaco, Monaco.
Valérie VialBiomedical Department, Centre Scientifique de Monaco, Monaco.
Xingkang HeDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institute, Stockholm, Sweden.
Damien AmbrosettiUniversity Côte d'Azur, Institute for Research on Cancer and Aging of Nice (IRCAN), CNRS UMR 7284; INSERM U1081, Centre Antoine Lacassagne, Nice, France.
Anna KamenskayaKekkan Biologics, Strasbourg, France.
Sylvie NegrierCentre Léon Bérard, University Claude Bernard Lyon, Lyon, France.
Jean-Christophe BernhardDepartment of Urology, Centre Hospitalier Universitaire (CHU) de Bordeaux, France.
Delphine BorchielliniDepartment of Medical Oncology, Centre Antoine Lacassagne, Nice, France.
Yihai CaoDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institute, Stockholm, Sweden.
Gilles PagèsBiomedical Department, Centre Scientifique de Monaco, Monaco.ORCID 0000-0002-8466-5610
Centre National de la Recherche Scientifique · FRScientific Centre of Monaco · MCKarolinska Institutet · SECentre Antoine Lacassagne · FRCentre Hospitalier Universitaire de Bordeaux · FRInternational University of Monaco · MCUniversité Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The efficacy of anti-angiogenic treatment by targeting VEGF/VEGF receptors in metastatic clear cell renal cell carcinoma (ccRCC) varies from patient to patient. Discovering the reasons behind this variability could lead to the identification of relevant therapeutic targets. Thus, we investigated the novel splice variants of VEGF that are less efficiently inhibited by anti-VEGF/VEGFR targeting than the conventional isoforms. By in silico analysis, we identified a novel splice acceptor in the last intron of the VEGF gene resulting in an insertion of 23 bp in VEGF mRNA. Such an insertion can shift the open-reading frame in previously described splice variants of VEGF (VEGF

Indexed as

Carcinoma, Renal CellAngiogenesis InhibitorsAnimalsCell ProliferationMiceNeovascularization, PathologicProtein IsoformsAngiogenesis InhibitorsProtein Isoformsalternative splicingangio/lymphangiogenesisrenal cell carcinomaresistance to antiangiogenicsVEGF

Identifiers

PMID36810959
PMCPMC10323879
OpenAlexW4321433609

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.