Evidence map›Paper›PMID 24940653›Full record

ArticleThe Journal of investigative dermatology2014

CD63 tetraspanin is a negative driver of epithelial-to-mesenchymal transition in human melanoma cells.

Antonella Lupia, Silvia Peppicelli, Ewa Witort, Francesca Bianchini, Vinicio Carloni, Nicola Pimpinelli, Carmelo Urso, Lorenzo Borgognoni, Sergio Capaccioli, Lido Calorini and 1 more

Abstract read
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In one paragraph

Article in The Journal of investigative dermatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.0field-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

22 citing papers in PubMed, 48 citations in OpenAlex.

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  17. Single-step RT-qPCR for detection of extracellular vesicle microRNAs in vivo: a time- and cost-effective method.American journal of physiology. Lung cellular and molecular physiology · 2020
    Article
  18. Multiplexed profiling of single-cell extracellular vesicles secretion.Proceedings of the National Academy of Sciences of the United States of America · 2019
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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

11 authors at 3 institutions in 1 country.

Antonella LupiaDepartment of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Florence, Italy.
Silvia PeppicelliDepartment of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Florence, Italy.
Ewa WitortDepartment of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Florence, Italy.
Francesca BianchiniDepartment of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Florence, Italy.
Vinicio CarloniDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Nicola PimpinelliClinical, Preventive and Oncologic Dermatology Section, Department Critical Care Medicine and Surgery, University of Florence, Florence, Italy.
Carmelo UrsoDepartment of Anatomic Pathology, Santa Maria Annunziata Hospital, Florence, Italy.
Lorenzo BorgognoniPlastic Surgery Unit, Regional Melanoma Referral Center, Tuscan Tumor Institute (ITT), Santa Maria Annunziata Hospital, Florence, Italy.
Sergio CapaccioliDepartment of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Florence, Italy.
Lido CaloriniDepartment of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Florence, Italy. Electronic address: lido.calorini@unifi.it.
Matteo LulliDepartment of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Florence, Italy. Electronic address: matteo.lulli@unifi.it.
University of Florence · ITOspedale Santa Maria Annunziata · ITTumour Institute of Tuscany · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The CD63 tetraspanin is highly expressed in the early stages of melanoma and decreases in advanced lesions, suggesting it as a possible suppressor of tumor progression. We employed loss- and gain-of-gene-function approaches to investigate the role of CD63 in melanoma progression and acquisition of the epithelial-to-mesenchymal transition (EMT) program. We used two human melanoma cell lines derived from primary tumors and one primary human melanoma cell line isolated from a cutaneous metastasis, differing by levels of CD63 expression. CD63-silenced melanoma cells showed enhanced motility and invasiveness with downregulation of E-cadherin and upregulation of N-cadherin and Snail. In parallel experiments, transient and stable ectopic expression of CD63 resulted in a robust reduction of cell motility, invasiveness, and protease activities, which was proportional to the increase in CD63 protein level. Transfected cells overexpressing the highest level of CD63 when transplanted into immunodeficient mice showed a reduced incidence and rate of tumor growth. Moreover, these cells showed a reduction of N-cadherin, Vimentin, Zeb1, and a-SMA, and a significant resistance to undergo an EMT program both in basal condition and in the following stimulation with TGFβ. Thus, our results establish a previously unreported mechanistic link between the tetraspanin CD63 and EMT abrogation in melanoma.

Indexed as

Disease ProgressionAnimalsCadherinsCell Line, TumorCell MovementDisease Models, AnimalEpithelial-Mesenchymal TransitionFemaleGene SilencingHeterograftsHumansMelanomaMiceMice, SCIDRNA, Small InterferingSkin NeoplasmsCadherinsCD63 protein, humanRNA, Small InterferingSnail Family Transcription FactorsTetraspanin 30Transcription Factors

Identifiers

PMID24940653
OpenAlexW2079521303

What OpenQuestion holds

Textmetadata
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.