Evidence map›Paper›PMID 31566767›Full record

ArticleThe EMBO journal2019

Notch and EGFR regulate apoptosis in progenitor cells to ensure gut homeostasis in Drosophila.

Tobias Reiff, Zeus A Antonello, Esther Ballesta-Illán, Laura Mira, Salvador Sala, Maria Navarro, Luis M Martinez, Maria Dominguez

Open access · hybridAbstract read
In one paragraph

Article in The EMBO journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

38 citing papers in PubMed, 68 citations in OpenAlex.

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  11. Notch Signaling in Drosophila Tumor Models.Advances in experimental medicine and biology · 2025
    Review
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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

8 authors at 1 institution in 1 country.

Tobias ReiffInstituto de Neurociencias, Consejo Superior de Investigaciones Científicas-Universidad Miguel Hernández (CSIC-UMH), Alicante, Spain.ORCID 0000-0001-6610-6148
Zeus A AntonelloInstituto de Neurociencias, Consejo Superior de Investigaciones Científicas-Universidad Miguel Hernández (CSIC-UMH), Alicante, Spain.ORCID 0000-0002-5933-6794
Esther Ballesta-IllánInstituto de Neurociencias, Consejo Superior de Investigaciones Científicas-Universidad Miguel Hernández (CSIC-UMH), Alicante, Spain.
Laura MiraInstituto de Neurociencias, Consejo Superior de Investigaciones Científicas-Universidad Miguel Hernández (CSIC-UMH), Alicante, Spain.
Salvador SalaInstituto de Neurociencias, Consejo Superior de Investigaciones Científicas-Universidad Miguel Hernández (CSIC-UMH), Alicante, Spain.
Maria NavarroInstituto de Neurociencias, Consejo Superior de Investigaciones Científicas-Universidad Miguel Hernández (CSIC-UMH), Alicante, Spain.
Luis M MartinezInstituto de Neurociencias, Consejo Superior de Investigaciones Científicas-Universidad Miguel Hernández (CSIC-UMH), Alicante, Spain.
Maria DominguezInstituto de Neurociencias, Consejo Superior de Investigaciones Científicas-Universidad Miguel Hernández (CSIC-UMH), Alicante, Spain.ORCID 0000-0002-3329-7862
Consejo Superior de Investigaciones Científicas · ES

Funding

Drosophila Transgenic RNAi Resource ProjectR01GM084947 · NIGMS · HARVARD MEDICAL SCHOOL · PI PERRIMON, NORBERT · 2008 to 2019
$9.8M
Deutsche Forschungsgesellschaft (DFG)Foundation BotinFundación Científica Asociación Española Contra el Cáncer (AECC) AECC CICPF16001DOMÍGeneralitat Valenciana (Regional Government of Valencia) PROMETEO/2017/146MEC|Consejo Superior de Investigaciones Científicas (CSIC) MICCIN BFU2015-64239-RMinisterio de Economía y Competitividad (MEC) SEV-2013-0317NIGMS NIH HHS R01 GM084947
6 · The paper itself

Abstract

The regenerative activity of adult stem cells carries a risk of cancer, particularly in highly renewable tissues. Members of the family of inhibitor of apoptosis proteins (IAPs) inhibit caspases and cell death, and are often deregulated in adult cancers; however, their roles in normal adult tissue homeostasis are unclear. Here, we show that regulation of the number of enterocyte-committed progenitor (enteroblast) cells in the adult Drosophila involves a caspase-mediated physiological apoptosis, which adaptively eliminates excess enteroblast cells produced by intestinal stem cells (ISCs) and, when blocked, can also lead to tumorigenesis. Importantly, we found that Diap1 is expressed by enteroblast cells and that loss and gain of Diap1 led to changes in enteroblast numbers. We also found that antagonistic interplay between Notch and EGFR signalling governs enteroblast life/death decisions via the Klumpfuss/WT1 and Lozenge/RUNX transcription regulators, which also regulate enteroblast differentiation and cell fate plasticity. These data provide new insights into how caspases drive adult tissue renewal and protect against the formation of tumours.

Indexed as

ApoptosisAnimalsCaspasesCell DifferentiationCell LineageDrosophila melanogasterDrosophila ProteinsEnterocytesErbB ReceptorsFemaleHomeostasisInhibitor of Apoptosis ProteinsIntestinesMaleReceptors, Invertebrate PeptideReceptors, NotchCaspasesDIAP1 protein, DrosophilaDrosophila ProteinsEgfr protein, DrosophilaErbB ReceptorsInhibitor of Apoptosis ProteinsN protein, DrosophilaReceptors, Invertebrate PeptideReceptors, Notchcaspaseintestinal enteroblastKlumpfuss/WT1Lozenge/RUNXphysiological apoptosis

Identifiers

PMID31566767
PMCPMC6826210
OpenAlexW2978552325

What Socratic holds

Textmetadata
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 Socratic graph.