Evidence map›Paper›PMID 28726765›Full record

ArticleInternational journal of molecular sciences2017

Oleic Acid Uptake Reveals the Rescued Enterocyte Phenotype of Colon Cancer Caco-2 by HT29-MTX Cells in Co-Culture Mode.

Emmanuelle Berger, Merian Nassra, Claude Atgié, Pascale Plaisancié, Alain Géloën

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

18 citing papers in PubMed, 29 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

5 authors at 4 institutions in 1 country.

Emmanuelle BergerUniv-Lyon, CarMeN Laboratory, Inserm U1060, INRA U1397, Université Claud Bernard Lyon1, INSA Lyon, Fr-69100 Villeurbanne, France. emmanuelle.danty@univ-lyon1.fr.
Merian NassraInstitut CBMN (Chimie et Biologie des Membranes & Nanoobjets)-UMR 5248 (CNRS-Bordeaux INP-Université de Bordeaux)-Equipe ClipIN-Bât B14-Ave G. St Hilaire, 33600 Pessac, France. nassra_nassra@yahoo.com.
Claude AtgiéInstitut CBMN (Chimie et Biologie des Membranes & Nanoobjets)-UMR 5248 (CNRS-Bordeaux INP-Université de Bordeaux)-Equipe ClipIN-Bât B14-Ave G. St Hilaire, 33600 Pessac, France. claude.atgie@enscbp.fr.
Pascale PlaisanciéUniv-Lyon, CarMeN Laboratory, Inserm U1060, INRA U1397, Université Claud Bernard Lyon1, INSA Lyon, Fr-69100 Villeurbanne, France. pascale.plaisancie@inserm.fr.
Alain GéloënUniv-Lyon, CarMeN Laboratory, Inserm U1060, INRA U1397, Université Claud Bernard Lyon1, INSA Lyon, Fr-69100 Villeurbanne, France. alain.geloen@insa-lyon.fr.
Inserm · FRInstitut Polytechnique de Bordeaux · FRUniversité Claude Bernard Lyon 1 · FRUniversité de Bordeaux · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastrointestinal epithelium is the unique route for nutrients and for many pharmaceuticals to enter the body. The present study aimed to analyze precisely whether co-culture of two colon cancer cell lines, mucus-producing cells HT29-MTX and enterocyte-like Caco-2 cells, ameliorate differentiation into an in vitro intestinal barrier model and the signaling pathways involved. Differentiated Caco-2 cells gene datasets were compared first to intestinal or cancer phenotypes and second to signaling pathway gene datasets. Experimental validations were performed in real-time experiments, immunochemistry, and gene expression analyses on Caco-2 versus co-cultures of Caco-2 and HT29-MTX (10%) cells. Partial maintenance of cancer-cell phenotype in differentiated Caco-2 cells was confirmed and fatty acids merged as potential regulators of cancer signaling pathways. HT29-MTX cells induced morphological changes in Caco-2 cells, slightly increased their proliferation rate and profoundly modified gene transcription of phenotype markers, fatty acid receptors, intracellular transporters, and lipid droplet components as well as functional responses to oleic acid. In vitro, enterocyte phenotype was rescued partially by co-culture of cancer cells with goblet cells and completed through oleic acid interaction with signaling pathways dysregulated in cancer cells.

Indexed as

PhenotypeCaco-2 CellsCell DifferentiationCell Line, TumorCell ProliferationCoculture TechniquesColonic NeoplasmsDatabases, GeneticEnterocytesGene Expression ProfilingGene Expression Regulation, NeoplasticHT29 CellsHumansIntestinal MucosaOleic AcidTranscription, GeneticOleic Acidcancer cell linesco-culturefatty acidsgene datasetsintestinal barriersignaling pathways

Identifiers

PMID28726765
PMCPMC5536061
OpenAlexW2736450902

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.