Evidence map›Paper›PMID 31937834›Full record

ArticleScientific reports2020

The ETS transcription factor ETV5 is a target of activated ALK in neuroblastoma contributing to increased tumour aggressiveness.

Liselot M Mus, Irina Lambertz, Shana Claeys, Candy Kumps, Wouter Van Loocke, Christophe Van Neste, Ganesh Umapathy, Marica Vaapil, Christoph Bartenhagen, Genevieve Laureys and 10 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 10% 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

15 citing papers in PubMed, 28 citations in OpenAlex.

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  5. Combination Therapies Targeting ALK-aberrant Neuroblastoma in Preclinical Models.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
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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

20 authors at 7 institutions in 3 countries.

Liselot M MusDepartment of Biomolecular Medicine, Ghent University, Ghent, Belgium.ORCID http://orcid.org/0000-0001-5738-0639
Irina LambertzDepartment of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Shana ClaeysDepartment of Biomolecular Medicine, Ghent University, Ghent, Belgium.ORCID http://orcid.org/0000-0002-1332-2653
Candy KumpsDepartment of Uro-gynaecology, Ghent University Hospital, Ghent, Belgium.
Wouter Van LoockeDepartment of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Christophe Van NesteDepartment of Biomolecular Medicine, Ghent University, Ghent, Belgium.ORCID http://orcid.org/0000-0002-5958-5731
Ganesh UmapathyDepartment of Medical Biochemistry and Cell Biology, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Marica VaapilTranslational Cancer Research, Lund University, Lund, Sweden.
Christoph BartenhagenDepartment of Experimental Pediatric Oncology, University Children's Hospital of Cologne, Medical Faculty, University of Cologne, 50937, Cologne, Germany.
Genevieve LaureysDepartment of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Olivier De WeverCancer Research Institute Ghent (CRIG), Ghent, Belgium.ORCID http://orcid.org/0000-0002-5453-760X
Daniel BexellTranslational Cancer Research, Lund University, Lund, Sweden.
Matthias FischerDepartment of Experimental Pediatric Oncology, University Children's Hospital of Cologne, Medical Faculty, University of Cologne, 50937, Cologne, Germany.ORCID http://orcid.org/0000-0003-1363-1242
Bengt HallbergDepartment of Medical Biochemistry and Cell Biology, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.ORCID http://orcid.org/0000-0003-2032-2616
Johannes SchulteDepartment of Paediatric Oncology and Haematology, University Children's Hospital Essen, Essen, Germany.
Bram De WildeDepartment of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Kaat DurinckDepartment of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Geertrui DeneckerDepartment of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Katleen De PreterDepartment of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Frank SpelemanDepartment of Biomolecular Medicine, Ghent University, Ghent, Belgium. franki.speleman@UGent.be.ORCID http://orcid.org/0000-0002-6628-8559
Ghent University · BEGhent University Hospital · BELund University · SEUniversity of Cologne · DEUniversity of Gothenburg · SEGerman Cancer Research Center · DEUniversity College Ghent · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuroblastoma is an aggressive childhood cancer arising from sympatho-adrenergic neuronal progenitors. The low survival rates for high-risk disease point to an urgent need for novel targeted therapeutic approaches. Detailed molecular characterization of the neuroblastoma genomic landscape indicates that ALK-activating mutations are present in 10% of primary tumours. Together with other mutations causing RAS/MAPK pathway activation, ALK mutations are also enriched in relapsed cases and ALK activation was shown to accelerate MYCN-driven tumour formation through hitherto unknown ALK-driven target genes. To gain further insight into how ALK contributes to neuroblastoma aggressiveness, we searched for known oncogenes in our previously reported ALK-driven gene signature. We identified ETV5, a bona fide oncogene in prostate cancer, as robustly upregulated in neuroblastoma cells harbouring ALK mutations, and show high ETV5 levels downstream of the RAS/MAPK axis. Increased ETV5 expression significantly impacted migration, invasion and colony formation in vitro, and ETV5 knockdown reduced proliferation in a murine xenograft model. We also established a gene signature associated with ETV5 knockdown that correlates with poor patient survival. Taken together, our data highlight ETV5 as an intrinsic component of oncogenic ALK-driven signalling through the MAPK axis and propose that ETV5 upregulation in neuroblastoma may contribute to tumour aggressiveness.

Indexed as

Cell ProliferationGene Expression Regulation, NeoplasticAnaplastic Lymphoma KinaseAnimalsApoptosisBiomarkers, TumorDNA-Binding ProteinsFemaleHumansMiceMice, NudeNeuroblastomaTranscription FactorsTumor Cells, CulturedXenograft Model Antitumor AssaysALK protein, humanAnaplastic Lymphoma KinaseBiomarkers, TumorDNA-Binding ProteinsETV5 protein, humanTranscription Factors

Identifiers

PMID31937834
PMCPMC6959226
OpenAlexW2999812390

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.