Evidence map›Paper›PMID 33575256›Full record

ArticleFrontiers in cell and developmental biology2020

A Semi-automated Organoid Screening Method Demonstrates Epigenetic Control of Intestinal Epithelial Differentiation.

Jenny Ostrop, Rosalie T Zwiggelaar, Marianne Terndrup Pedersen, François Gerbe, Korbinian Bösl, Håvard T Lindholm, Alberto Díez-Sánchez, Naveen Parmar, Silke Radetzki, Jens Peter von Kries and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2020. 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
2.2field-weighted citation impact, top 12% 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, 27 citations in OpenAlex.

  1. Article
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  3. Engineered organoids for biomedical applications.Advanced drug delivery reviews · 2023
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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

14 authors at 7 institutions in 5 countries.

Jenny OstropCentre of Molecular Inflammation Research (CEMIR), Department of Clinical and Molecular Medicine (IKOM), NTNU - Norwegian University of Science and Technology, Trondheim, Norway.
Rosalie T ZwiggelaarCentre of Molecular Inflammation Research (CEMIR), Department of Clinical and Molecular Medicine (IKOM), NTNU - Norwegian University of Science and Technology, Trondheim, Norway.
Marianne Terndrup PedersenBRIC - Biotech Research and Innovation Centre, University of Copenhagen, Copenhagen, Denmark.
François GerbeCancer Biology Department, Institute of Functional Genomics, University of Montpellier, Montpellier, France.
Korbinian BöslDepartment of Bioinformatics, Computational Biological Unit, University of Bergen, Bergen, Norway.
Håvard T LindholmCentre of Molecular Inflammation Research (CEMIR), Department of Clinical and Molecular Medicine (IKOM), NTNU - Norwegian University of Science and Technology, Trondheim, Norway.
Alberto Díez-SánchezCentre of Molecular Inflammation Research (CEMIR), Department of Clinical and Molecular Medicine (IKOM), NTNU - Norwegian University of Science and Technology, Trondheim, Norway.
Naveen ParmarCentre of Molecular Inflammation Research (CEMIR), Department of Clinical and Molecular Medicine (IKOM), NTNU - Norwegian University of Science and Technology, Trondheim, Norway.
Silke RadetzkiScreening Unit, Leibniz-Forschungsinstitut für Molekulare Pharmakologie, Berlin, Germany.
Jens Peter von KriesScreening Unit, Leibniz-Forschungsinstitut für Molekulare Pharmakologie, Berlin, Germany.
Philippe JayCancer Biology Department, Institute of Functional Genomics, University of Montpellier, Montpellier, France.
Kim B JensenBRIC - Biotech Research and Innovation Centre, University of Copenhagen, Copenhagen, Denmark.
Cheryl ArrowsmithStructural Genomics Consortium, University of Toronto, Toronto, ON, Canada.
Menno J OudhoffCentre of Molecular Inflammation Research (CEMIR), Department of Clinical and Molecular Medicine (IKOM), NTNU - Norwegian University of Science and Technology, Trondheim, Norway.
Norwegian University of Science and Technology · NOLeibniz-Forschungsinstitut für Molekulare Pharmakologie · DEUniversité de Montpellier · FRNovo Nordisk Foundation · DKPrincess Margaret Cancer Centre · CAUniversity of Bergen · NOUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intestinal organoids are an excellent model to study epithelial biology. Yet, the selection of analytical tools to accurately quantify heterogeneous organoid cultures remains limited. Here, we developed a semi-automated organoid screening method, which we applied to a library of highly specific chemical probes to identify epigenetic regulators of intestinal epithelial biology. The role of epigenetic modifiers in adult stem cell systems, such as the intestinal epithelium, is still undefined. Based on this resource dataset, we identified several targets that affected epithelial cell differentiation, including HDACs, EP300/CREBBP, LSD1, and type I PRMTs, which were verified by complementary methods. For example, we show that inhibiting type I PRMTs, which leads enhanced epithelial differentiation, blocks the growth of adenoma but not normal organoid cultures. Thus, epigenetic probes are powerful tools to study intestinal epithelial biology and may have therapeutic potential.

Indexed as

bioimage analysisCREBBPEP300epigenetic modifiersintestinal stem cell biologyorganoidsPRMT1

Identifiers

PMID33575256
PMCPMC7872100
OpenAlexW3125485476

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.