Evidence map›Paper›PMID 34249925›Full record

ArticleFrontiers in cell and developmental biology2021

Wnt Activity and Cell Proliferation Are Coupled to Extracellular Vesicle Release in Multiple Organoid Models.

Gyöngyvér Orsolya Sándor, András Áron Soós, Péter Lörincz, Lívia Rojkó, Tünde Harkó, Levente Bogyó, Tamás Tölgyes, Attila Bursics, Edit I Buzás, Judit Moldvay and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  3. Article
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  5. Article
  6. The application of patient-derived organoid in the research of lung cancer.Cellular oncology (Dordrecht, Netherlands) · 2023
    Review
  7. Review
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  10. Article
  11. Review
  12. Pre-clinical Models of Metastasis in Pancreatic Cancer.Frontiers in cell and developmental biology · 2021
    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

11 authors at 4 institutions in 1 country.

Gyöngyvér Orsolya SándorDepartment of Genetics, Cell and Immunobiology, Semmelweis University, Budapest, Hungary.
András Áron SoósDepartment of Genetics, Cell and Immunobiology, Semmelweis University, Budapest, Hungary.
Péter LörinczDepartment of Anatomy, Cell and Developmental Biology, Eötvös Loránd University of Sciences, Budapest, Hungary.
Lívia Rojkó1st Department of Pulmonology, National Korányi Institute of Pulmonology, Budapest, Hungary.
Tünde HarkóDepartment of Pathology, National Korányi Institute of Pulmonology, Budapest, Hungary.
Levente BogyóDepartment of Thoracic Surgery, Semmelweis University and National Institute of Oncology, Budapest, Hungary.
Tamás TölgyesDepartment of General Surgery and Surgical Oncology, Uzsoki Hospital, Budapest, Hungary.
Attila BursicsDepartment of General Surgery and Surgical Oncology, Uzsoki Hospital, Budapest, Hungary.
Edit I BuzásDepartment of Genetics, Cell and Immunobiology, Semmelweis University, Budapest, Hungary.
Judit Moldvay1st Department of Pulmonology, National Korányi Institute of Pulmonology, Budapest, Hungary.
Zoltán WienerDepartment of Genetics, Cell and Immunobiology, Semmelweis University, Budapest, Hungary.
Semmelweis University · HUOrszágos Korányi Tbc és Pulmonológiai Intézet · HUUzsoki Hospital · HUHungarian Academy of Sciences · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extracellular vesicles (EV) are considered as a potential tool for early disease diagnosis; however, factors modifying EV release remain partially unknown. By using patient-derived organoids that capture the cellular heterogeneity of epithelial tissues, here we studied the connection between the Wnt-producing microniche and EV secretion in multiple tissues. Although nearly all cells in pancreatic ductal (PD) and pancreatic ductal adenocarcinoma (PDAC) samples expressed porcupine (PORCN), an enzyme critical for Wnt secretion, only a subpopulation of lung bronchiolar (NL) and lung adenocarcinoma (LUAD) organoid cells produced active Wnt. The microniche for proliferating cells was shaped not only by PORCN + cells in NL and LUAD organoids but also by fibroblast-derived EVs. This effect could be blocked by using Wnt secretion inhibitors. Whereas inhibiting Wnt secretion in PD NL or LUAD organoids critically changed both cell proliferation and EV release, these were uncoupled from each other in PDAC. Sorting for CD133 identified a cell population in the LUAD microniche that produced organoids with a high percentage of PORCN + and proliferating cells and an elevated EV secretion, which may explain that CD133 marks LUAD cells with malignant behavior. Collectively, we show here that high cell proliferation rate, induced by Wnt pathway activation, is coupled to a higher EV release, a critical finding that may be considered when developing EV-based diagnostic tools.

Indexed as

CD133exosomelung adenocarcinomalung cancerorganoidpancreatic ductal adenocarcinomaprominin-1

Identifiers

PMID34249925
PMCPMC8264557
OpenAlexW3173787458

What OpenQuestion holds

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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.