Evidence map›Paper›PMID 26474461›Full record

ArticleOncotarget2015

Caveolin-1-negative head and neck squamous cell carcinoma primary tumors display increased epithelial to mesenchymal transition and prometastatic properties.

Alain C Jung, Anne-Marie Ray, Ludivine Ramolu, Christine Macabre, Florian Simon, Fanny Noulet, Anne-Florence Blandin, Guillaume Renner, Maxime Lehmann, Laurence Choulier and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.7field-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

25 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
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  14. The Roles of Integrin α5β1 in Human Cancer.OncoTargets and therapy · 2020
    Review
  15. Article
  16. Clinical Value ofScientific reports · 2018
    Article
  17. Article
  18. Review
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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

14 authors at 3 institutions in 2 countries.

Alain C JungLaboratoire de Biologie Tumorale, EA 3430 Université de Strasbourg, CRLC Paul Strauss, Strasbourg, France.
Anne-Marie RayUniversité de Strasbourg, LBP, CNRS UMR 7213, Illkirch, France.
Ludivine RamoluLaboratoire de Biologie Tumorale, EA 3430 Université de Strasbourg, CRLC Paul Strauss, Strasbourg, France.
Christine MacabreLaboratoire de Biologie Tumorale, EA 3430 Université de Strasbourg, CRLC Paul Strauss, Strasbourg, France.
Florian SimonUniversité de Strasbourg, LBP, CNRS UMR 7213, Illkirch, France.
Fanny NouletUniversité de Strasbourg, LBP, CNRS UMR 7213, Illkirch, France.
Anne-Florence BlandinUniversité de Strasbourg, LBP, CNRS UMR 7213, Illkirch, France.
Guillaume RennerUniversité de Strasbourg, LBP, CNRS UMR 7213, Illkirch, France.
Maxime LehmannUniversité de Strasbourg, LBP, CNRS UMR 7213, Illkirch, France.
Laurence ChoulierUniversité de Strasbourg, LBP, CNRS UMR 7213, Illkirch, France.
Horst KesslerInstitute for Advanced Study and Center of Integrated Protein Studies, Technische Universität München, Department Chemie, Garching, Germany.
Joseph AbecassisLaboratoire de Biologie Tumorale, EA 3430 Université de Strasbourg, CRLC Paul Strauss, Strasbourg, France.
Monique DontenwillUniversité de Strasbourg, LBP, CNRS UMR 7213, Illkirch, France.
Sophie MartinUniversité de Strasbourg, LBP, CNRS UMR 7213, Illkirch, France.
Université de Strasbourg · FRCentre National de la Recherche Scientifique · FRTechnical University of Munich · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Distant metastases arise in 20-30% of patients with squamous cell carcinoma of the head and neck (HNSCC) in the 2 years following treatment. Therapeutic options are limited and the outcome of the patients is poor. The identification of predictive biomarkers of patient at risk for distant metastasis and therapies are urgently needed. We previously identified a clinical subgroup, called "R1" characterized by high propensity for rapid distant metastasis. Here, we showed that "R1" patients do not or at very low level express caveolin-1 (Cav1). Low or no expression of Cav1 is of bad prognosis. Disappearance of Cav1 enables cells to undergo epithelial-mesenchymal transition (EMT). EMT is associated with enhanced migration and invasion. Our study uncovered a new target, α5β1 integrin. Targeting α5β1 integrins might not only prevent metastasis of HNSCC but also delay the development of the primary tumor by reducing tumor cell viability. Cav1 detection might be taken into consideration in the future in the clinic not only to identify patients at high risk of metastasis but also to select patient who might benefit from an anti-integrin therapy.

Indexed as

Cell MovementEpithelial-Mesenchymal TransitionBiomarkers, TumorCarcinoma, Squamous CellCaveolin 1Cell Line, TumorDown-RegulationGene Expression Regulation, NeoplasticHead and Neck NeoplasmsHumansIntegrin alpha5beta1Kaplan-Meier EstimatePrognosisRNA InterferenceSignal TransductionSquamous Cell Carcinoma of Head and NeckBiomarkers, TumorCAV1 protein, humanCaveolin 1Integrin alpha5beta1caveolin-1head and neck cancerintegrinsmetastasis

Identifiers

PMID26474461
PMCPMC4747196
OpenAlexW2276576377

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.