Evidence map›Paper›PMID 29196606›Full record

ArticleThe Journal of biological chemistry2018

Control of endothelial cell tube formation by Notch ligand intracellular domain interactions with activator protein 1 (AP-1).

Zary Forghany, Francesca Robertson, Alicia Lundby, Jesper V Olsen, David A Baker

Abstract read
In one paragraph

Article in The Journal of biological chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. NOTCH3 CADASIL Variant Receptor Aggregation Requires NOTCH3 Wild-Type Receptors: Identification of Highly Selective Inhibitors That Block the Process.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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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

5 authors.

Zary ForghanyFrom the Department of Molecular Cell Biology, Leiden University Medical Center, 2300 RC Leiden, The Netherlands and.
Francesca RobertsonFrom the Department of Molecular Cell Biology, Leiden University Medical Center, 2300 RC Leiden, The Netherlands and.
Alicia LundbyNovo Nordisk Foundation Center for Protein Research and.
Jesper V OlsenNovo Nordisk Foundation Center for Protein Research and.
David A BakerFrom the Department of Molecular Cell Biology, Leiden University Medical Center, 2300 RC Leiden, The Netherlands and d.baker@lumc.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Notch signaling is a ubiquitous signal transduction pathway found in most if not all metazoan cell types characterized to date. It is indispensable for cell differentiation as well as tissue growth, tissue remodeling, and apoptosis. Although the canonical Notch signaling pathway is well characterized, accumulating evidence points to the existence of multiple, less well-defined layers of regulation. In this study, we investigated the function of the intracellular domain (ICD) of the Notch ligand Delta-like 4 (DLL4). We provide evidence that the DLL4 ICD is required for normal DLL4 subcellular localization. We further show that it is cleaved and interacts with the JUN proto-oncogene, which forms part of the activator protein 1 (AP-1) transcription factor complex. Mechanistically, the DLL4 ICD inhibited JUN binding to DNA and thereby controlled the expression of JUN target genes, including

Indexed as

Signal TransductionAdaptor Proteins, Signal TransducingCalcium-Binding ProteinsHEK293 CellsHumansHuman Umbilical Vein Endothelial CellsIntercellular Signaling Peptides and ProteinsProtein DomainsProto-Oncogene MasProto-Oncogene Proteins c-junReceptors, NotchTranscription Factor AP-1Adaptor Proteins, Signal TransducingCalcium-Binding ProteinsDLL4 protein, humanIntercellular Signaling Peptides and ProteinsMAS1 protein, humanProto-Oncogene MasProto-Oncogene Proteins c-junReceptors, NotchTranscription Factor AP-1angiogenesisAP1 transcription factor (AP-1)gene regulationNotch pathwaysignaling

Identifiers

PMID29196606
PMCPMC5787801

What OpenQuestion 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 OpenQuestion graph.