Evidence map›Paper›PMID 24376606›Full record

ArticlePloS one2013

Identification of SLAMF3 (CD229) as an inhibitor of hepatocellular carcinoma cell proliferation and tumour progression.

Ingrid Marcq, Rémy Nyga, Flora Cartier, Rabbind Singh Amrathlal, Christèle Ossart, Hakim Ouled-Haddou, Hussein Ghamlouch, Antoine Galmiche, Denis Chatelain, Luciane Lamotte and 7 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. 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
0.7field-weighted citation impact, top 28% 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, 20 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

17 authors at 4 institutions in 1 country.

Ingrid MarcqINSERM UMR925 and EA 4666 UFR de Médecine, CAP-Santé (FED 4231), Université de Picardie Jules Verne, Amiens, France.
Rémy NygaINSERM UMR925 and EA 4666 UFR de Médecine, CAP-Santé (FED 4231), Université de Picardie Jules Verne, Amiens, France.
Flora CartierINSERM UMR925 and EA 4666 UFR de Médecine, CAP-Santé (FED 4231), Université de Picardie Jules Verne, Amiens, France ; INSERM U1053, Laboratoire de Physiologie du Cancer du Foie, Université Bordeaux Segalen, 146, rue Léo Saignat, Bordeaux, France.
Rabbind Singh AmrathlalINSERM UMR925 and EA 4666 UFR de Médecine, CAP-Santé (FED 4231), Université de Picardie Jules Verne, Amiens, France.
Christèle OssartService d'hématologie Clinique et de thérapie cellulaire Centre Hospitalier Universitaire sud, Amiens, France.
Hakim Ouled-HaddouINSERM UMR925 and EA 4666 UFR de Médecine, CAP-Santé (FED 4231), Université de Picardie Jules Verne, Amiens, France.
Hussein GhamlouchINSERM UMR925 and EA 4666 UFR de Médecine, CAP-Santé (FED 4231), Université de Picardie Jules Verne, Amiens, France.
Antoine GalmicheService de Biochimie, Centre Hospitalier Universitaire sud, Amiens, France.
Denis ChatelainService d'Anatomie Pathologique, Centre Hospitalier Universitaire sud, Amiens, France.
Luciane LamotteINSERM UMR925 and EA 4666 UFR de Médecine, CAP-Santé (FED 4231), Université de Picardie Jules Verne, Amiens, France.
Véronique DebuysscherINSERM UMR925 and EA 4666 UFR de Médecine, CAP-Santé (FED 4231), Université de Picardie Jules Verne, Amiens, France.
Vincent FuentesINSERM UMR925 and EA 4666 UFR de Médecine, CAP-Santé (FED 4231), Université de Picardie Jules Verne, Amiens, France ; Service d'Immunologie, Centre Hospitalier Universitaire sud, Amiens, France.
Eric Nguyen-KhacService Hepato-Gastroenterologie, Centre Hospitalier Universitaire sud, Amiens, France.
Jean-Marc RegimbeauService de chirurgie digestive Centre Hospitalier Universitaire sud, Amiens, France.
Jean-Pierre MarolleauINSERM UMR925 and EA 4666 UFR de Médecine, CAP-Santé (FED 4231), Université de Picardie Jules Verne, Amiens, France ; Service d'hématologie Clinique et de thérapie cellulaire Centre Hospitalier Universitaire sud, Amiens, France.
Sylvain LatourIRNEM U768, Hôpital Necker enfants maladies, Paris, France.
Hicham BouhlalINSERM UMR925 and EA 4666 UFR de Médecine, CAP-Santé (FED 4231), Université de Picardie Jules Verne, Amiens, France ; Service d'hématologie Clinique et de thérapie cellulaire Centre Hospitalier Universitaire sud, Amiens, France.
Centre Hospitalier Universitaire Amiens-Picardie · FRUniversité de Picardie Jules Verne · FRInserm · FRHôpital Necker-Enfants Malades · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although hepatocellular carcinoma (HCC) is one of the most common malignancies and constitutes the third leading cause of cancer-related deaths, the underlying molecular mechanisms are not fully understood. In the present study, we demonstrate for the first time that hepatocytes express signalling lymphocytic activation molecule family member 3 (SLAMF3/CD229) but not other SLAMF members. We provide evidence to show that SLAMF3 is involved in the control of hepatocyte proliferation and in hepatocellular carcinogenesis. SLAMF3 expression is significantly lower in primary human HCC samples and HCC cell lines than in human healthy primary hepatocytes. In HCC cell lines, the restoration of high levels of SLAMF3 expression inhibited cell proliferation and migration and enhanced apoptosis. Furthermore, SLAMF3 expression was associated with inhibition of HCC xenograft progression in the nude mouse model. The restoration of SLAMF3 expression levels also decreased the phosphorylation of MAPK ERK1/2, JNK and mTOR. In samples from resected HCC patients, SLAMF3 expression levels were significantly lower in tumorous tissues than in peritumoral tissues. Our results identify SLAMF3 as a specific marker of normal hepatocytes and provide evidence for its potential role in the control of proliferation of HCC cells.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsAntigens, CDCarcinoma, HepatocellularCell Line, TumorDisease ProgressionHumansInjections, SubcutaneousLiver NeoplasmsMaleMAP Kinase Kinase 4MiceMice, NudeMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Neoplasm TransplantationAntigens, CDLY9 protein, humanLy9 protein, mouseMAP Kinase Kinase 4Mitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3mTOR protein, mouseSignaling Lymphocytic Activation Molecule FamilyTOR Serine-Threonine Kinases

Identifiers

PMID24376606
PMCPMC3869749
OpenAlexW2078402197

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.