Evidence map›Paper›PMID 26222204›Full record

ArticleeLife2015

The Notch-mediated hyperplasia circuitry in Drosophila reveals a Src-JNK signaling axis.

Diana M Ho, S K Pallavi, Spyros Artavanis-Tsakonas

Open access · goldAbstract read
In one paragraph

Article in eLife, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

24 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Notch Signaling in Drosophila Tumor Models.Advances in experimental medicine and biology · 2025
    Review
  5. Article
  6. Regulation of Notch signaling by non-muscle myosin II Zipper in Drosophila.Cellular and molecular life sciences : CMLS · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Modelling Cooperative Tumorigenesis inBioMed research international · 2018
    Review
  20. Article
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

3 authors at 1 institution in 2 countries.

Diana M HoDepartment of Cell Biology, Harvard Medical School, Boston, United States.
S K PallaviDepartment of Cell Biology, Harvard Medical School, Boston, United States.
Spyros Artavanis-TsakonasDepartment of Cell Biology, Harvard Medical School, Boston, United States.
Harvard University · US

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
Notch Signaling in Mammary Development and TumorigenesisR01CA098402 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI ARTAVANIS-TSAKONAS, SPYRIDON · 2003 to 2013
$3.6M
NCI NIH HHS CA 098402NCI NIH HHS R01 CA098402NIH HHS P40 OD018537
6 · The paper itself

Abstract

Notch signaling controls a wide range of cell fate decisions during development and disease via synergistic interactions with other signaling pathways. Here, through a genome-wide genetic screen in Drosophila, we uncover a highly complex Notch-dependent genetic circuitry that profoundly affects proliferation and consequently hyperplasia. We report a novel synergistic relationship between Notch and either of the non-receptor tyrosine kinases Src42A and Src64B to promote hyperplasia and tissue disorganization, which results in cell cycle perturbation, JAK/STAT signal activation, and differential regulation of Notch targets. Significantly, the JNK pathway is responsible for the majority of the phenotypes and transcriptional changes downstream of Notch-Src synergy. We previously reported that Notch-Mef2 also activates JNK, indicating that there are commonalities within the Notch-dependent proliferation circuitry; however, the current data indicate that Notch-Src accesses JNK in a significantly different fashion than Notch-Mef2.

Indexed as

Cell ProliferationHyperplasiaMAP Kinase Signaling SystemAnimalsDrosophilaDrosophila ProteinsMAP Kinase Kinase 4Protein-Tyrosine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins pp60(c-src)Receptors, NotchDrosophila ProteinsMAP Kinase Kinase 4N protein, DrosophilaProtein-Tyrosine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins pp60(c-src)Receptors, NotchSrc42A protein, DrosophilaSrc64B protein, Drosophilacell biologydevelopmental biologyD. melanogasterhyperplasiaJNKNotchproliferationSrcstem cells

Identifiers

PMID26222204
PMCPMC4517436
OpenAlexW1901254290

What Socratic 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 Socratic graph.