Evidence map›Paper›PMID 33627749›Full record

ArticleScientific reports2021

Notch signaling drives development of Barrett's metaplasia from Dclk1-positive epithelial tuft cells in the murine gastric mucosa.

Bettina Kunze, Moritz Middelhoff, H Carlo Maurer, Tatiana Agibalova, Akanksha Anand, Anne-Marie Bührer, Hsin-Yu Fang, Theresa Baumeister, Katja Steiger, Julia Strangmann and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Pleiotropic effects of DCLK1 in cancer and cancer stem cells.Frontiers in molecular biosciences · 2022
    Review
  11. Review
  12. Article
  13. Short histological kaleidoscope - recent findings in histology. Part IV.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    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

13 authors at 3 institutions in 2 countries.

Bettina Kunze *Klinik und Poliklinik für Innere Medizin II, Technical University of Munich, Munich, Germany.
Moritz Middelhoff *Klinik und Poliklinik für Innere Medizin II, Technical University of Munich, Munich, Germany. moritz.middelhoff@tum.de.
H Carlo MaurerKlinik und Poliklinik für Innere Medizin II, Technical University of Munich, Munich, Germany.
Tatiana AgibalovaKlinik und Poliklinik für Innere Medizin II, Technical University of Munich, Munich, Germany.
Akanksha AnandKlinik und Poliklinik für Innere Medizin II, Technical University of Munich, Munich, Germany.
Anne-Marie BührerKlinik und Poliklinik für Innere Medizin II, Technical University of Munich, Munich, Germany.
Hsin-Yu FangKlinik und Poliklinik für Innere Medizin II, Technical University of Munich, Munich, Germany.
Theresa BaumeisterKlinik und Poliklinik für Innere Medizin II, Technical University of Munich, Munich, Germany.
Katja SteigerInstitute of Pathology, Technical University of Munich, Munich, Germany.
Julia StrangmannKlinik und Poliklinik für Innere Medizin II, Technical University of Munich, Munich, Germany.
Roland M SchmidKlinik und Poliklinik für Innere Medizin II, Technical University of Munich, Munich, Germany.
Timothy C WangDepartment of Medicine, Columbia University Medical Center, New York, NY, USA.
Michael QuanteKlinik und Poliklinik für Innere Medizin II, Technical University of Munich, Munich, Germany. michael.quante@uniklinik-freiburg.de.
Technical University of Munich · DEColumbia University Irving Medical Center · USUniversity Medical Center Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Barrett's esophagus (BE) is a precursor to esophageal adenocarcinoma (EAC), but its cellular origin and mechanism of neoplastic progression remain unresolved. Notch signaling, which plays a key role in regulating intestinal stem cell maintenance, has been implicated in a number of cancers. The kinase Dclk1 labels epithelial post-mitotic tuft cells at the squamo-columnar junction (SCJ), and has also been proposed to contribute to epithelial tumor growth. Here, we find that genetic activation of intracellular Notch signaling in epithelial Dclk1-positive tuft cells resulted in the accelerated development of metaplasia and dysplasia in a mouse model of BE (pL2.Dclk1.N2IC mice). In contrast, genetic ablation of Notch receptor 2 in Dclk1-positive cells delayed BE progression (pL2.Dclk1.N2fl mice), and led to increased secretory cell differentiation. The accelerated BE progression in pL2.Dclk1.N2IC mice correlated with changes to the transcriptomic landscape, most notably for the activation of oncogenic, proliferative pathways in BE tissues, in contrast to upregulated Wnt signalling in pL2.Dclk1.N2fl mice. Collectively, our data show that Notch activation in Dclk1-positive tuft cells in the gastric cardia can contribute to BE development.

Indexed as

AdenocarcinomaAnimalsBarrett EsophagusCarcinogenesisCardiaCell DifferentiationCell ProliferationDisease Models, AnimalDoublecortin-Like KinasesEpithelial CellsEsophageal NeoplasmsEsophagusGastric MucosaMetaplasiaMiceReceptors, NotchDclk1 protein, mouseDoublecortin-Like KinasesReceptors, Notch

Identifiers

PMID33627749
PMCPMC7904766
OpenAlexW3132844032

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.