Evidence map›Paper›PMID 29698439›Full record

ArticlePloS one2018

TNF differentially regulates ganglioside biosynthesis and expression in breast cancer cell lines.

Justine H Dewald, Sumeyye Cavdarli, Agata Steenackers, Clément P Delannoy, Marlène Mortuaire, Corentin Spriet, Maxence Noël, Sophie Groux-Degroote, Philippe Delannoy

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Ganglioside GD2 Contributes to a Stem-Like Phenotype in Intrahepatic Cholangiocarcinoma.Liver international : official journal of the International Association for the Study of the Liver · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. 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

9 authors at 2 institutions in 1 country.

Justine H DewaldUniversity of Lille, Structural and Functional Glycobiology Unit, UMR CNRS 8576, Lille, France.
Sumeyye CavdarliUniversity of Lille, Structural and Functional Glycobiology Unit, UMR CNRS 8576, Lille, France.
Agata SteenackersUniversity of Lille, Structural and Functional Glycobiology Unit, UMR CNRS 8576, Lille, France.
Clément P DelannoyUniversity of Lille, Structural and Functional Glycobiology Unit, UMR CNRS 8576, Lille, France.
Marlène MortuaireUniversity of Lille, Structural and Functional Glycobiology Unit, UMR CNRS 8576, Lille, France.
Corentin SprietUniversity of Lille, Bio Imaging Center Lille, Lille, France.
Maxence NoëlUniversity of Lille, Structural and Functional Glycobiology Unit, UMR CNRS 8576, Lille, France.
Sophie Groux-DegrooteUniversity of Lille, Structural and Functional Glycobiology Unit, UMR CNRS 8576, Lille, France.
Philippe DelannoyUniversity of Lille, Structural and Functional Glycobiology Unit, UMR CNRS 8576, Lille, France.ORCID 0000-0001-6467-7553
Centre National de la Recherche Scientifique · FRUniversité de Lille · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gangliosides are glycosphingolipids concentrated in glycolipid-enriched membrane microdomains. Mainly restricted to the nervous system in healthy adult, complex gangliosides such as GD3 and GD2 have been shown to be involved in aggressiveness and metastasis of neuro-ectoderm derived tumors such as melanoma and neuroblastoma. GD3 synthase (GD3S), the key enzyme that controls the biosynthesis of complex gangliosides, was shown to be over-expressed in Estrogen Receptor (ER)-negative breast cancer tumors, and associated with a decreased overall survival of patients. We previously demonstrated that GD3S expression in ER-negative breast cancer cells induced a proliferative phenotype and an increased tumor growth. In addition, our results clearly indicate that Tumor Necrosis Factor (TNF) induced GD3S over-expression in breast cancer cells via NFκB pathway. In this study, we analyzed the effect of TNF on ganglioside biosynthesis and expression in breast cancer cells from different molecular subtypes. We showed that TNF up-regulated the expression of GD3S in MCF-7 and Hs578T cells, whereas no change was observed for MDA-MB-231. We also showed that TNF induced an increased expression of complex gangliosides at the cell surface of a small proportion of MCF-7 cells. These results demonstrate that TNF differentially regulates gangliosides expression in breast cancer cell lines and establish a possible link between inflammation at the tumor site environment, expression of complex gangliosides and tumor development.

Indexed as

Breast NeoplasmsCell Line, TumorFatty AcidsFemaleGangliosidesGene Expression Regulation, NeoplasticGlycosyltransferasesHumansMCF-7 CellsMicroscopy, FluorescenceSialyltransferasesSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationTumor Necrosis Factor-alphaalpha-N-acetylneuraminate alpha-2,8-sialyltransferaseFatty AcidsGangliosidesGlycosyltransferasesSialyltransferasesTumor Necrosis Factor-alpha

Identifiers

PMID29698439
PMCPMC5919650
OpenAlexW2800907237

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.