Evidence map›Paper›PMID 27633923›Full record

ArticleGut2017

Human pluripotent stem cell-derived acinar/ductal organoids generate human pancreas upon orthotopic transplantation and allow disease modelling.

Meike Hohwieler, Anett Illing, Patrick C Hermann, Tobias Mayer, Marianne Stockmann, Lukas Perkhofer, Tim Eiseler, Justin S Antony, Martin Müller, Susanne Renz and 18 more

Open access · hybridAbstract read
In one paragraph

Article in Gut, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 143 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
143citing papers in PubMed, 1 pooled it
9.9field-weighted citation impact, top 1% 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

143 citing papers in PubMed, 1 synthesis or guideline pooled it, 209 citations in OpenAlex.

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83 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

28 authors at 8 institutions in 2 countries.

Meike HohwielerDepartment of Internal Medicine I, University Medical Center Ulm, Ulm, Germany.
Anett IllingDepartment of Internal Medicine I, University Medical Center Ulm, Ulm, Germany.
Patrick C HermannDepartment of Internal Medicine I, University Medical Center Ulm, Ulm, Germany.
Tobias MayerDepartment of Internal Medicine I, University Medical Center Ulm, Ulm, Germany.
Marianne StockmannDepartment of Internal Medicine I, University Medical Center Ulm, Ulm, Germany.
Lukas PerkhoferDepartment of Internal Medicine I, University Medical Center Ulm, Ulm, Germany.
Tim EiselerDepartment of Internal Medicine I, University Medical Center Ulm, Ulm, Germany.
Justin S AntonyDepartment of Pediatrics I, Pediatric Infectiology and Immunology, Translational Genomics and Gene Therapy in Pediatrics, University of Tuebingen, Tuebingen, Germany.
Martin MüllerDepartment of Internal Medicine I, University Medical Center Ulm, Ulm, Germany.
Susanne RenzDepartment of Internal Medicine I, University Medical Center Ulm, Ulm, Germany.
Chao-Chung KuoMedical Faculty, IZKF Computational Biology Research Group, RWTH Aachen University, Aachen, Germany.
Qiong LinMedical Faculty, Department of Cell Biology, Institute for Biomedical Engineering, RWTH Aachen University, Aachen, Germany.
Matthias SendlerDepartment of Medicine A, University Medicine, Ernst-Moritz-Arndt-University, Greifswald, Germany.
Markus BreunigDepartment of Internal Medicine I, University Medical Center Ulm, Ulm, Germany.
Susanne M KleidermanDepartment of Internal Medicine I, University Medical Center Ulm, Ulm, Germany.
André LechelDepartment of Internal Medicine I, University Medical Center Ulm, Ulm, Germany.
Martin ZenkerInstitute of Human Genetics, University Hospital, Magdeburg, Germany.
Michael LeichsenringDepartment of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Ulm, Germany.
Jonas RosendahlDepartment of Internal Medicine I, Division of Medicine, Martin-Luther-University Halle-Wittenberg, Halle (Saale), Germany.
Martin ZenkeMedical Faculty, Department of Cell Biology, Institute for Biomedical Engineering, RWTH Aachen University, Aachen, Germany.
Bruno SainzDepartment of Biochemistry, Universidad Autónoma de Madrid, Instituto de Investigaciones Biomédicas "Alberto Sols" CSIC-UAM, Madrid, Spain.
Julia MayerleDepartment of Medicine A, University Medicine, Ernst-Moritz-Arndt-University, Greifswald, Germany.
Ivan G CostaMedical Faculty, IZKF Computational Biology Research Group, RWTH Aachen University, Aachen, Germany.
Thomas SeufferleinDepartment of Internal Medicine I, University Medical Center Ulm, Ulm, Germany.
Michael KormannDepartment of Pediatrics I, Pediatric Infectiology and Immunology, Translational Genomics and Gene Therapy in Pediatrics, University of Tuebingen, Tuebingen, Germany.
Martin WagnerDepartment of Internal Medicine I, University Medical Center Ulm, Ulm, Germany.
Stefan LiebauInstitute of Neuroanatomy, Eberhard Karls University Tuebingen, Tuebingen, Germany.
Alexander KlegerDepartment of Internal Medicine I, University Medical Center Ulm, Ulm, Germany.
Universität Ulm · DERWTH Aachen University · DEUniversity of Tübingen · DEUniversität Greifswald · DEInstituto de Investigaciones Biomédicas Sols-Morreale · ESMartin Luther University Halle-Wittenberg · DEUniversity Hospital Magdeburg · DEUniversity Hospital Ulm · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe generation of acinar and ductal cells from human pluripotent stem cells (PSCs) is a poorly studied process, although various diseases arise from this compartment.

designWe designed a straightforward approach to direct human PSCs towards pancreatic organoids resembling acinar and ductal progeny.

resultsExtensive phenotyping of the organoids not only shows the appropriate marker profile but also ultrastructural, global gene expression and functional hallmarks of the human pancreas in the dish. Upon orthotopic transplantation into immunodeficient mice, these organoids form normal pancreatic ducts and acinar tissue resembling fetal human pancreas without evidence of tumour formation or transformation. Finally, we implemented this unique phenotyping tool as a model to study the pancreatic facets of cystic fibrosis (CF). For the first time, we provide evidence that in vitro

conclusionsTaken together, our platform provides novel opportunities to model pancreatic disease and development, screen for disease-rescuing agents and to test therapeutic procedures.

Indexed as

Disease Models, AnimalAcinar CellsAnimalsCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorGene Expression ProfilingGenetic TherapyHumansMiceOrganoidsPancreasPancreatic DuctsPhenotypePluripotent Stem CellsRNA, MessengerCystic Fibrosis Transmembrane Conductance RegulatorRNA, MessengerCYSTIC FIBROSISPANCREASSTEM CELLS

Identifiers

PMID27633923
PMCPMC5534761
OpenAlexW2520537726

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.