Evidence map›Paper›PMID 41106385›Full record

ArticleStem cell reports2025

Interplay of EGFR, JNK, and ROS signaling in soma-germline communication in the Drosophila testis.

Maria Alvarez, Fani Papagiannouli

Abstract read
In one paragraph

Article in Stem cell reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Maria AlvarezMedway School of Pharmacy, Universities of Kent and Greenwich, Chatham, UK.
Fani PapagiannouliMedway School of Pharmacy, Universities of Kent and Greenwich, Chatham, UK. Electronic address: f.papagiannouli-227@kent.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell communication via signaling exchange plays a pivotal role in multicellular development for building up functional tissues and organs. In the Drosophila testis, a pair of somatic cyst cells (CCs) encapsulate the germline that differentiates through close-range EGFR signaling activation. The Dlg/Scrib/Lgl polarity complex and clathrin-mediated endocytosis attenuate EGFR signaling in CCs, and loss of their function leads to EGFR overactivation and death of the neighboring germ cells. Here, we show that EGFR overactivation leads to upregulation of JNK and p38 signaling in CCs and ROS levels in germ cells destined to die. Our data uncover a bidirectional-feedback mechanism between JNK signaling and ROS who regulate each other, while reducing the levels of either JNK or ROS restored germ cell survival. This study provides a framework of how polarity and cellular trafficking regulate the output of multiple signaling responses cell-intrinsically and across cells, to coordinate tissue-specific responses and maintain homeostasis.

Indexed as

Cell CommunicationDrosophila melanogasterDrosophila ProteinsErbB ReceptorsGerm CellsMAP Kinase Signaling SystemReactive Oxygen SpeciesReceptors, Invertebrate PeptideTestisAnimalsDrosophilaMaleSignal TransductionDrosophila ProteinsEgfr protein, DrosophilaErbB ReceptorsReactive Oxygen SpeciesReceptors, Invertebrate Peptidecell communicationDlgDrosophila testisEGFRendocytosisgermlineJNKpolarityRab35ROS

Identifiers

PMID41106385
PMCPMC12790739

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.