Evidence map›Paper›PMID 24499734›Full record

ArticleThe Journal of investigative dermatology2014

TGF-β-induced (TGFBI) protein in melanoma: a signature of high metastatic potential.

Laura Lauden, Johan Siewiera, Wahid Boukouaci, Kiran Ramgolam, Samia Mourah, Celeste Lebbe, Dominique Charron, Fawzi Aoudjit, Nabila Jabrane-Ferrat, Reem Al-Daccak

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 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
1.9field-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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

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  14. Weighted Gene Co-Expression Network Analysis Identifies Hub Genes Associated with Occurrence and Prognosis of Oral Squamous Cell Carcinoma.Medical science monitor : international medical journal of experimental and clinical research · 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

10 authors at 6 institutions in 2 countries.

Laura LaudenInstitut National de la Santé et de la Recherche Médicale (INSERM) UMRS 940, University Paris 7-Denis Diderot, AP-HP, Saint Louis Hospital, Paris, France.
Johan SiewieraINSERM UMR 1043 and CNRS UMR 5282, University Toulouse III Paul Sabatier, Toulouse, France.
Wahid BoukouaciInstitut National de la Santé et de la Recherche Médicale (INSERM) UMRS 940, University Paris 7-Denis Diderot, AP-HP, Saint Louis Hospital, Paris, France.
Kiran RamgolamInstitut National de la Santé et de la Recherche Médicale (INSERM) UMRS 940, University Paris 7-Denis Diderot, AP-HP, Saint Louis Hospital, Paris, France.
Samia MourahInstitut National de la Santé et de la Recherche Médicale (INSERM) UMRS 940, University Paris 7-Denis Diderot, AP-HP, Saint Louis Hospital, Paris, France; Pharmacology-Genetics Laboratory, University Paris 7-Denis Diderot, AP-HP, Saint Louis Hospital, Paris, France.
Celeste LebbeDermatology Department, University Paris 7-Denis Diderot, AP-HP, Saint Louis Hospital, Paris, France; Institut National de la Santé et de la Recherche Médicale (INSERM) UMR 976, University Paris 7-Denis Diderot, AP-HP, Saint Louis Hospital, Paris, France.
Dominique CharronInstitut National de la Santé et de la Recherche Médicale (INSERM) UMRS 940, University Paris 7-Denis Diderot, AP-HP, Saint Louis Hospital, Paris, France; Jean Dausset Laboratory, University Paris 7-Denis Diderot, AP-HP, Saint Louis Hospital, Paris, France.
Fawzi AoudjitCentre de Recherche du CHU de Québec, Université Laval, Québec, Canada.
Nabila Jabrane-FerratINSERM UMR 1043 and CNRS UMR 5282, University Toulouse III Paul Sabatier, Toulouse, France. Electronic address: nabila.jabrane-ferrat@inserm.fr.
Reem Al-DaccakInstitut National de la Santé et de la Recherche Médicale (INSERM) UMRS 940, University Paris 7-Denis Diderot, AP-HP, Saint Louis Hospital, Paris, France. Electronic address: reem.al-daccak@inserm.fr.
Inserm · FRUniversité Paris Cité · FRAssistance Publique – Hôpitaux de Paris · FRCentre hospitalier de l'Université Laval · CADélégation Paris 7 · FRUniversité Toulouse III - Paul Sabatier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor-produced extracellular matrix (ECM) proteins can be key elements in tumor growth and metastasis. Transforming growth factor beta-inducible (TGFBI) protein is a secreted ECM component that can have dual function in cancer, acting as tumor suppressor or promoter. Although TGFBI is expressed in human melanoma cells, the exact role it might have in melanoma metastasis remains elusive. Assessing the expression and secretion of TGFBI, we show that human metastatic melanomas express and secrete significantly higher amounts of TGFBI, compared with nevus lesions and primary melanoma tumors. Intravenous injection of highly metastatic human melanoma cells expressing shRNA that targets TGFBI assigns a critical role for TGFBI in the formation of melanoma distal metastases in nude mice. In vivo assays demonstrate that TGFBI silencing does not interfere with melanoma cells' dissemination to distal sites but rather with their proliferation and outgrowth within new microenvironment. In line, TGFBI silencing increases melanoma cells motility/invasion/extravasation in vitro but interferes with their progression through the cell cycle, drastically reducing their proliferation. Furthermore, we show that TGFBI is a regulator of cyclins and cyclin-dependent kinases in melanoma. Collectively, our data describe a mechanism of melanoma metastatic outgrowth via promotion of growth/survival by the ECM protein TGFBI.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsApoptosisbetaIG-H3 ProteinBiopsyCell AdhesionCell CycleCell Line, TumorCell MovementCell ProliferationCell SurvivalExtracellular Matrix ProteinsFemaleGene Expression ProfilingGene SilencingHumansbetaIG-H3 ProteinExtracellular Matrix ProteinsRNA, Small InterferingTransforming Growth Factor beta

Identifiers

PMID24499734
OpenAlexW2026187359

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.