Evidence map›Paper›PMID 39726234›Full record

ArticleLiver international : official journal of the International Association for the Study of the Liver2025

Ganglioside GD2 Contributes to a Stem-Like Phenotype in Intrahepatic Cholangiocarcinoma.

Antonella Mannini, Mirella Pastore, Alessia Giachi, Margherita Correnti, Elena Spínola Lasso, Tiziano Lottini, Benedetta Piombanti, Ignazia Tusa, Elisabetta Rovida, Cédric Coulouarn and 19 more

Abstract read
In one paragraph

Article in Liver international : official journal of the International Association for the Study of the Liver, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
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  3. Review
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

29 authors.

Antonella ManniniDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Mirella PastoreDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Alessia GiachiDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Margherita CorrentiDepartment of Biomedical Sciences for Health, University of Milan, Milan, Italy.
Elena Spínola LassoDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Tiziano LottiniDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Benedetta PiombantiDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Ignazia TusaDepartment of Experimental and Clinical Biomedical Sciences 'Mario Serio', University of Florence, Florence, Italy.
Elisabetta RovidaDepartment of Experimental and Clinical Biomedical Sciences 'Mario Serio', University of Florence, Florence, Italy.
Cédric CoulouarnUniv Rennes, Inserm, Inra, Institut NUMECAN (Nutrition Metabolisms and Cancer)-UMR_S 1241, UMR_A 1341, Rennes, France.
Jesper B AndersenBiotech Research and Innovation Centre, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0003-1760-5244
Monika LewinskaBiotech Research and Innovation Centre, University of Copenhagen, Copenhagen, Denmark.
Claudia CampaniDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
V Lokesh BattulaDivision of Cancer Medicine, Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Bin YuanDivision of Cancer Medicine, Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Massimo AureliDepartment of Medical Biotechnology and Translational Medicine, University of Milan, Milan, Italy.
Emma V CarsanaDepartment of Medical Biotechnology and Translational Medicine, University of Milan, Milan, Italy.
Caterina Peraldo NeiaFondazione Edo Ed Elvo Tempia Valenta, Biella, Italy.
Paola OstanoFondazione Edo Ed Elvo Tempia Valenta, Biella, Italy.
Alessia TaniDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Daniele NosiDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Anna VanniDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Laura MaggiDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Luca Di TommasoHumanitas Research Hospital-IRCCS, Pathology Unit, Rozzano, Italy.
Giuseppina ComitoDepartment of Experimental and Clinical Biomedical Sciences 'Mario Serio', University of Florence, Florence, Italy.
Stefania MadiaiDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Annarosa ArcangeliDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Fabio MarraDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.ORCID 0000-0001-8629-0878
Chiara RaggiDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.ORCID 0000-0003-2473-3535

Funding

Cassa di Risparmio di Pistoia e PesciaCOST Action EURO-CHOLANGIO-NETEURO-CHOLANGIO-NET and Precision-BTC-Network granted by COST ACTION CA18122EURO-CHOLANGIO-NET and Precision-BTC-Network granted by COST ACTION CA22125Fondazione. AIRC per la ricerca sul cancro ETS
6 · The paper itself

Abstract

BACKGROUND &

aimsGD2, a member of the ganglioside (GS) family (sialic acid-containing glycosphingolipids), is a potential biomarker of cancer stem cells (CSC) in several tumours. However, the possible role of GD2 and its biosynthetic enzyme, GD3 synthase (GD3S), in intrahepatic cholangiocarcinoma (iCCA) has not been explored.

methodsThe stem-like subset of two iCCA cell lines was enriched by sphere culture (SPH) and compared to monolayer parental cells (MON). GS profiles were evaluated by chromatography, after feeding with radioactive sphingosine. Membrane GD2 expression was evaluated by FACS, and the expression of enzymes of GS biosynthesis was analysed by RT-qPCR. The modulation of stem features by GS was investigated in vitro and in vivo using GD3S-overexpressing cells and corroborated by global transcriptomic analysis.

resultsGS composition was markedly different comparing SPH and MON. Among complex GS, iCCA-SPH showed increased GD2 levels, in agreement with the high expression levels of GD3 and GM2/GD2 synthases. iCCA cells overexpressing GD3S had higher sphere-forming ability, invasive properties and drug resistance than parental cells. NOD/SCID mice implanted with CCLP1 cells overexpressing GD3S developed larger tumours than control cells. By global transcriptomic analysis, ontology investigation identified 74 processes shared by the iCCA-SPH and GD3S-transfected cells, with enrichment for development and morphogenesis processes, MAPK signalling and locomotion. In a cohort of patients with iCCA, GD3S expression was correlated with lymph node invasion, indicating a possible relevance of GD3S in the clinical setting.

conclusionsThe profile of GS derivatives regulates the stem-like properties of iCCA cells.

Indexed as

Bile Duct NeoplasmsCholangiocarcinomaGangliosidesNeoplastic Stem CellsSialyltransferasesAnimalsCell Line, TumorHumansMiceMice, SCIDPhenotypealpha-N-acetylneuraminate alpha-2,8-sialyltransferaseganglioside, GD2GangliosidesSialyltransferasescancer stem cellscancer stemness biomarkerGD2 gangliosideGD3 synthase (o ST8SIA1)intrahepatic cholangiocarcinoma

Identifiers

PMID39726234
PMCPMC11684508

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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.