Evidence map›Paper›PMID 26110787›Full record

ArticlePloS one2015

Gamma-smooth muscle actin expression is associated with epithelial-mesenchymal transition and stem-like properties in hepatocellular carcinoma.

Nassima Benzoubir, Charlotte Mussini, Charlène Lejamtel, Alexandre Dos Santos, Claire Guillaume, Christophe Desterke, Didier Samuel, Christian Bréchot, Marie-Françoise Bourgeade, Catherine Guettier

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. October in focus in HCB.Histochemistry and cell biology · 2025
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  12. Fascin Induces Epithelial-Mesenchymal Transition of Cholangiocarcinoma Cells by Regulating Wnt/β-Catenin Signaling.Medical science monitor : international medical journal of experimental and clinical research · 2016
    Article
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 3 institutions in 1 country.

Nassima BenzoubirInserm, Unité 785, Villejuif, F-94800, France; Univ Paris-Sud, UMR-S 785, Villejuif, F-94800, France; DHU Hepatinov, Villejuif, France.
Charlotte MussiniAP-HP Hôpital Kremlin-Bicêtre, Service d'Anatomopathologie, Paris, France; DHU Hepatinov, Villejuif, France.
Charlène LejamtelInserm, Unité 785, Villejuif, F-94800, France; Univ Paris-Sud, UMR-S 785, Villejuif, F-94800, France.
Alexandre Dos SantosInserm, Unité 785, Villejuif, F-94800, France; Univ Paris-Sud, UMR-S 785, Villejuif, F-94800, France; DHU Hepatinov, Villejuif, France.
Claire GuillaumeAP-HP Hôpital Kremlin-Bicêtre, Service d'Anatomopathologie, Paris, France; DHU Hepatinov, Villejuif, France.
Christophe DesterkeSFR André Lwoff, Villejuif, F-94800, France; DHU Hepatinov, Villejuif, France.
Didier SamuelInserm, Unité 785, Villejuif, F-94800, France; Univ Paris-Sud, UMR-S 785, Villejuif, F-94800, France; AP-HP Hôpital Paul Brousse, Centre Hépatobiliaire, Villejuif, France; DHU Hepatinov, Villejuif, France.
Christian BréchotInserm, Unité 785, Villejuif, F-94800, France; Univ Paris-Sud, UMR-S 785, Villejuif, F-94800, France; Institut Pasteur, Paris, France.
Marie-Françoise BourgeadeInserm, Unité 785, Villejuif, F-94800, France; Univ Paris-Sud, UMR-S 785, Villejuif, F-94800, France; AP-HP Hôpital Paul Brousse, Centre Hépatobiliaire, Villejuif, France; DHU Hepatinov, Villejuif, France.
Catherine GuettierInserm, Unité 785, Villejuif, F-94800, France; Univ Paris-Sud, UMR-S 785, Villejuif, F-94800, France; AP-HP Hôpital Kremlin-Bicêtre, Service d'Anatomopathologie, Paris, France; DHU Hepatinov, Villejuif, France.
Université Paris-Sud · FRAssistance Publique – Hôpitaux de Paris · FRLaboratoire d'études sur les monothéismes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsThe prognosis of hepatocellular carcinoma (HCC) is hampered by frequent tumour recurrence and metastases. Epithelial-Mesenchymal Transition (EMT) is now recognized as a key process in tumour invasion, metastasis and the generation of cancer initiating cells. The morphological identification of EMT in tumour samples from the expression of novel mesenchymal markers could provide relevant prognostic information and aid in understanding the metastatic process.

methodsThe expression of Smooth Muscle Actins was studied using immunofluorescence and immunohistochemistry assays in cultured liver cells during an induced EMT process and in liver specimens from adult and paediatric HCC series.

resultsWe report here that in HCC cell lines treated with TGF-β and in HCC specimens, the expression of αSMA, a known mesenchymal marker of EMT, could never be detected. In addition, our in vitro studies identified the enteric form of SMA, γSMA, as being a marker of EMT. Moreover, this SMA isoform was expressed in 46% of 58 tumours from 42 adult HCC patients and in 90% of 16 tumours from 12 paediatric HCC patients. Interestingly, this expression was significantly correlated with poor tumour differentiation and progenitor cell features characterized by the expression of EpCAM and K19.

conclusionTaken together, our results support the conclusion that γSMA expression in HCC is strongly correlated with the EMT process, HCC aggressiveness and the identification of cancer stem cells. This correlation suggests that γSMA represents a novel and powerful marker to predict HCC progression.

Indexed as

Epithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticActinsAdultAgedAntigens, NeoplasmBiomarkersCarcinoma, HepatocellularCell Adhesion MoleculesCell DifferentiationCell Line, TumorCohort StudiesEpithelial Cell Adhesion MoleculeFemaleHumansKeratin-19ACTG2 protein, humanActinsAntigens, NeoplasmBiomarkersCell Adhesion MoleculesEPCAM protein, humanEpithelial Cell Adhesion MoleculeKeratin-19Recombinant ProteinsTransforming Growth Factor beta

Identifiers

PMID26110787
PMCPMC4482489
OpenAlexW2134922740

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.