Evidence map›Paper›PMID 32963234›Full record

ArticleNature communications2020

VAV2 signaling promotes regenerative proliferation in both cutaneous and head and neck squamous cell carcinoma.

L Francisco Lorenzo-Martín, Natalia Fernández-Parejo, Mauricio Menacho-Márquez, Sonia Rodríguez-Fdez, Javier Robles-Valero, Sonia Zumalave, Salvatore Fabbiano, Gloria Pascual, Juana M García-Pedrero, Antonio Abad and 12 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.1field-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

32 citing papers in PubMed, 44 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

22 authors at 6 institutions in 2 countries.

L Francisco Lorenzo-MartínCentro de Investigación del Cáncer, CSIC-University of Salamanca, 37007, Salamanca, Spain.ORCID http://orcid.org/0000-0003-4717-9338
Natalia Fernández-Parejo *Centro de Investigación del Cáncer, CSIC-University of Salamanca, 37007, Salamanca, Spain.
Mauricio Menacho-Márquez *Centro de Investigación del Cáncer, CSIC-University of Salamanca, 37007, Salamanca, Spain.
Sonia Rodríguez-FdezCentro de Investigación del Cáncer, CSIC-University of Salamanca, 37007, Salamanca, Spain.ORCID http://orcid.org/0000-0001-5369-2969
Javier Robles-ValeroCentro de Investigación del Cáncer, CSIC-University of Salamanca, 37007, Salamanca, Spain.
Sonia ZumalaveCenter for Research in Molecular Medicine and Chronic Diseases (CiMUS), University of Santiago de Compostela, 15782, Santiago de Compostela, Spain.ORCID http://orcid.org/0000-0002-2108-1861
Salvatore FabbianoCentro de Investigación del Cáncer, CSIC-University of Salamanca, 37007, Salamanca, Spain.ORCID http://orcid.org/0000-0003-0768-6028
Gloria PascualInstitute for Research in Biomedicine, 33011, Barcelona, Spain.ORCID http://orcid.org/0000-0003-3810-6647
Juana M García-PedreroCentro de Investigación Biomédica en Red de Cáncer (CIBERONC), CSIC-University of Salamanca, 37007, Salamanca, Spain.
Antonio AbadCentro de Investigación del Cáncer, CSIC-University of Salamanca, 37007, Salamanca, Spain.
María C García-MacíasCentro de Investigación del Cáncer, CSIC-University of Salamanca, 37007, Salamanca, Spain.ORCID http://orcid.org/0000-0002-5929-4926
Nazareno GonzálezCentro de Investigación del Cáncer, CSIC-University of Salamanca, 37007, Salamanca, Spain.ORCID http://orcid.org/0000-0003-4013-3396
Pablo Lorenzano-MennaLaboratory of Molecular Oncology and National University of Quilmes, Buenos Aires, B1876BXD, Argentina.
Miguel A PavónInstitut Català d'Oncologia, 08908, L'Hospitalet de Llobregat, Spain.
Rogelio González-SarmientoCentro de Investigación del Cáncer, CSIC-University of Salamanca, 37007, Salamanca, Spain.
Carmen SegrellesCentro de Investigación Biomédica en Red de Cáncer (CIBERONC), CSIC-University of Salamanca, 37007, Salamanca, Spain.
Jesús M ParamioCentro de Investigación Biomédica en Red de Cáncer (CIBERONC), CSIC-University of Salamanca, 37007, Salamanca, Spain.ORCID http://orcid.org/0000-0001-7520-3177
José M C TubíoCenter for Research in Molecular Medicine and Chronic Diseases (CiMUS), University of Santiago de Compostela, 15782, Santiago de Compostela, Spain.
Juan P RodrigoCentro de Investigación Biomédica en Red de Cáncer (CIBERONC), CSIC-University of Salamanca, 37007, Salamanca, Spain.ORCID http://orcid.org/0000-0003-3063-0890
Salvador A BenitahInstitute for Research in Biomedicine, 33011, Barcelona, Spain.ORCID http://orcid.org/0000-0002-9059-5049
Myriam CuadradoCentro de Investigación del Cáncer, CSIC-University of Salamanca, 37007, Salamanca, Spain.ORCID http://orcid.org/0000-0001-9410-1205
Xosé R BusteloCentro de Investigación del Cáncer, CSIC-University of Salamanca, 37007, Salamanca, Spain. xbustelo@usal.es.ORCID http://orcid.org/0000-0001-9398-6072
Universidad de Salamanca · ESUniversidade de Santiago de Compostela · ESCentro de Investigación Biomédica en Red de Enfermedades Respiratorias · ESInstitució Catalana de Recerca i Estudis Avançats · ESInstitute for Research in Biomedicine · ESNational University of Quilmes · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regenerative proliferation capacity and poor differentiation are histological features usually linked to poor prognosis in head and neck squamous cell carcinoma (hnSCC). However, the pathways that regulate them remain ill-characterized. Here, we show that those traits can be triggered by the RHO GTPase activator VAV2 in keratinocytes present in the skin and oral mucosa. VAV2 is also required to maintain those traits in hnSCC patient-derived cells. This function, which is both catalysis- and RHO GTPase-dependent, is mediated by c-Myc- and YAP/TAZ-dependent transcriptomal programs associated with regenerative proliferation and cell undifferentiation, respectively. High levels of VAV2 transcripts and VAV2-regulated gene signatures are both associated with poor hnSCC patient prognosis. These results unveil a druggable pathway linked to the malignancy of specific SCC subtypes.

Indexed as

Cell ProliferationAnimalsCell DifferentiationDisease Models, AnimalEpidermisGene Expression Regulation, NeoplasticGene Knockdown TechniquesGTP PhosphohydrolasesHead and Neck NeoplasmsHumansHyperplasiaKeratinocytesMiceMice, KnockoutMucous MembranePrognosisGTP PhosphohydrolasesProto-Oncogene Proteins c-vavRNA, MessengerVAV2 protein, human

Identifiers

PMID32963234
PMCPMC7508832
OpenAlexW3088909758

What OpenQuestion holds

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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.