Evidence map›Paper›PMID 25313138›Full record

ArticleOncotarget2014

Caveolin-1 is down-regulated in alveolar rhabdomyosarcomas and negatively regulates tumor growth.

Juan Huertas-Martínez, Santiago Rello-Varona, David Herrero-Martín, Ignasi Barrau, Silvia García-Monclús, Miguel Sáinz-Jaspeado, Laura Lagares-Tena, Yaiza Núñez-Álvarez, Silvia Mateo-Lozano, Jaume Mora and 9 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. TheMolecules (Basel, Switzerland) · 2024
    Article
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  6. Article
  7. Article
  8. Article
  9. Caveolin-1: An Oxidative Stress-Related Target for Cancer Prevention.Oxidative medicine and cellular longevity · 2017
    Review
  10. Article
  11. Article
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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 5 institutions in 1 country.

Juan Huertas-MartínezSarcoma research group, Molecular Oncology Lab, Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain.
Santiago Rello-VaronaSarcoma research group, Molecular Oncology Lab, Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain.
David Herrero-MartínSarcoma research group, Molecular Oncology Lab, Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain.
Ignasi BarrauSarcoma research group, Molecular Oncology Lab, Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain.
Silvia García-MonclúsSarcoma research group, Molecular Oncology Lab, Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain.
Miguel Sáinz-JaspeadoSarcoma research group, Molecular Oncology Lab, Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain.
Laura Lagares-TenaSarcoma research group, Molecular Oncology Lab, Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain.
Yaiza Núñez-ÁlvarezInstitut de Medicina Predictiva i Personalitzada del Càncer, Badalona, Barcelona, Spain.
Silvia Mateo-LozanoDevelopmental Tumor Biology Laboratory, Hospital Sant Joan de Deu, Barcelona, Spain.
Jaume MoraDevelopmental Tumor Biology Laboratory, Hospital Sant Joan de Deu, Barcelona, Spain.
Josep RomaBiomedical Research Unit, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Nuria ToranBiomedical Research Unit, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Sebastian MoranCancer Epigenetics and Biology Programme (PEBC), Bellvitge Biomedical Research Institute (IDIBELL), L' Hospitalet de Llobregat, Barcelona, Spain.
Roser López-AlemanySarcoma research group, Molecular Oncology Lab, Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain.
Soledad GallegoBiomedical Research Unit, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Manel EstellerCancer Epigenetics and Biology Programme (PEBC), Bellvitge Biomedical Research Institute (IDIBELL), L' Hospitalet de Llobregat, Barcelona, Spain.
Miguel A PeinadoInstitut de Medicina Predictiva i Personalitzada del Càncer, Badalona, Barcelona, Spain.
Xavier García Del MuroSarcoma research group, Molecular Oncology Lab, Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain.
Oscar M TiradoSarcoma research group, Molecular Oncology Lab, Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain.
Institut d'Investigació Biomédica de Bellvitge · ESVall d'Hebron Hospital Universitari · ESBellvitge University Hospital · ESHospital Sant Joan de Déu Barcelona · ESInstitute of Predictive and Personalized Medicine of Cancer · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rhabdomyosarcoma is the most common soft tissue sarcoma of childhood and adolescence. Despite advances in therapy, patients with histological variant of rhabdomyosarcoma known as alveolar rhabdomyosarcoma (ARMS) have a 5-year survival of less than 30%. Caveolin-1 (CAV1), encoding the structural component of cellular caveolae, is a suggested tumor suppressor gene involved in cell signaling. In the present study we report that compared to other forms of rhabdomyosarcoma (RMS) CAV1 expression is either undetectable or very low in ARMS cell lines and tumor samples. DNA methylation analysis of the promoter region and azacytidine-induced re-expression suggest the involvement of epigenetic mechanisms in the silencing of CAV1. Reintroduction of CAV1 in three of these cell lines impairs their clonogenic capacity and promotes features of muscular differentiation. In vitro, CAV1-expressing cells show high expression of Caveolin-3 (CAV3), a muscular differentiation marker. Blockade of MAPK signaling is also observed. In vivo, CAV1-expressing xenografts show growth delay, features of muscular differentiation and increased cell death. In summary, our results suggest that CAV1 could function as a potent tumor suppressor in ARMS tumors. Inhibition of CAV1 function therefore, could contribute to aberrant cell proliferation, leading to ARMS development.

Indexed as

AnimalsCaveolin 1Cell DeathCell DifferentiationCell Line, TumorCell ProliferationDown-RegulationEpigenomicsGene Expression Regulation, NeoplasticGenetic TherapyHeterograftsHumansMiceMice, NudeRhabdomyosarcoma, AlveolarSignal TransductionCaveolin 1

Identifiers

PMID25313138
PMCPMC4259434
OpenAlexW1923777609

What OpenQuestion holds

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LicenceCC BY
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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.