Evidence map›Paper›PMID 37380797›Full record

ArticleCellular and molecular life sciences : CMLS2023

Human pancreatic ductal organoids with controlled polarity provide a novel ex vivo tool to study epithelial cell physiology.

Árpád Varga, Tamara Madácsy, Marietta Görög, Aletta Kiss, Petra Susánszki, Viktória Szabó, Boldizsár Jójárt, Krisztina Dudás, Gyula Farkas, Edit Szederkényi and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

9 citing papers in PubMed, 12 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

15 authors at 1 institution in 1 country.

Árpád VargaDepartment of Medicine, University of Szeged, Szeged, Hungary.
Tamara MadácsyDepartment of Medicine, University of Szeged, Szeged, Hungary.
Marietta GörögDepartment of Medicine, University of Szeged, Szeged, Hungary.
Aletta KissDepartment of Medicine, University of Szeged, Szeged, Hungary.
Petra SusánszkiDepartment of Medicine, University of Szeged, Szeged, Hungary.
Viktória SzabóDepartment of Medicine, University of Szeged, Szeged, Hungary.
Boldizsár JójártDepartment of Medicine, University of Szeged, Szeged, Hungary.
Krisztina DudásDepartment of Medicine, University of Szeged, Szeged, Hungary.
Gyula FarkasDepartment of Surgery, University of Szeged, Szeged, Hungary.
Edit SzederkényiDepartment of Surgery, University of Szeged, Szeged, Hungary.
György LázárDepartment of Surgery, University of Szeged, Szeged, Hungary.
Attila FarkasHCEMM-USZ Functional Cell Biology and Immunology Advanced Core Facility, University of Szeged, Szeged, Hungary.
Ferhan AyaydinHCEMM-USZ Functional Cell Biology and Immunology Advanced Core Facility, University of Szeged, Szeged, Hungary.
Petra PallagiDepartment of Medicine, University of Szeged, Szeged, Hungary.
József MaléthDepartment of Medicine, University of Szeged, Szeged, Hungary. jozsefmaleth1@gmail.com.ORCID http://orcid.org/0000-0001-5768-3090
University of Szeged · HU

Funding

Horizon 2020 Framework Programme 739593Magyar Tudományos Akadémia LP2017-18/2017
6 · The paper itself

Abstract

Epithelial ion and fluid secretion determine the physiological functions of a broad range of organs, such as the lung, liver, or pancreas. The molecular mechanism of pancreatic ion secretion is challenging to investigate due to the limited access to functional human ductal epithelia. Patient-derived organoids may overcome these limitations, however direct accessibility of the apical membrane is not solved. In addition, due to the vectorial transport of ions and fluid the intraluminal pressure in the organoids is elevated, which may hinder the study of physiological processes. To overcome these, we developed an advanced culturing method for human pancreatic organoids based on the removal of the extracellular matrix that induced an apical-to-basal polarity switch also leading to reversed localization of proteins with polarized expression. The cells in the apical-out organoids had a cuboidal shape, whereas their resting intracellular Ca

Indexed as

Epithelial CellsPancreasBiological AssayEpitheliumHumansLiver3D cultureApical-outCFTRDuctal cellOrganoid

Identifiers

PMID37380797
PMCPMC10307727
OpenAlexW4382393412

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.