Evidence map›Paper›PMID 28472949›Full record

ArticleJournal of translational medicine2017

Distinct gene expression profiles associated with Notch ligands Delta-like 4 and Jagged1 in plaque material from peripheral artery disease patients: a pilot study.

Giorgio Aquila, Cinzia Fortini, Antonio Pannuti, Serena Delbue, Micaela Pannella, Marco Bruno Morelli, Cristiana Caliceti, Fausto Castriota, Monica de Mattei, Alessia Ongaro and 7 more

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

20 citing papers in PubMed, 33 citations in OpenAlex.

  1. Ticagrelor IncreasesInternational journal of molecular sciences · 2020
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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

17 authors at 7 institutions in 3 countries.

Giorgio AquilaDepartment of Medical Sciences, University of Ferrara, Ferrara, Italy.
Cinzia FortiniDepartment of Medical Sciences, University of Ferrara, Ferrara, Italy.
Antonio PannutiDepartment of Genetics and Stanley Scott Cancer Center, Louisiana State University Health Sciences Center and Louisiana Cancer Research Consortium, New Orleans, LA, USA.
Serena DelbueDepartment of Biomedical, Surgical and Dental SciencesUniversity of Milan, Milan, Italy.
Micaela PannellaGoldyneSavad Institute of Gene Therapy, Hadassah-Hebrew University Medical Center, 91120, Jerusalem, Israel.
Marco Bruno MorelliIRCCS Neuromed, Angio-Cardio-Neurology Department, Pozzilli, Italy.
Cristiana CalicetiDepartment of Chemistry "G. Ciamician", University of Bologna, Bologna, Italy.
Fausto CastriotaMaria Cecilia Hospital, GVM Care & Research, E.S. Health Science Foundation, Cotignola, Italy.
Monica de MatteiDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, Via Fossato di Mortara 64/B, 44121, Ferrara, Italy.
Alessia OngaroDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, Via Fossato di Mortara 64/B, 44121, Ferrara, Italy.
Agnese PellatiDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, Via Fossato di Mortara 64/B, 44121, Ferrara, Italy.
Pasquale FerranteDepartment of Biomedical, Surgical and Dental SciencesUniversity of Milan, Milan, Italy.
Lucio MieleDepartment of Genetics and Stanley Scott Cancer Center, Louisiana State University Health Sciences Center and Louisiana Cancer Research Consortium, New Orleans, LA, USA.
Luigi TavazziMaria Cecilia Hospital, GVM Care & Research, E.S. Health Science Foundation, Cotignola, Italy.
Roberto FerrariDepartment of Medical Sciences, University of Ferrara, Ferrara, Italy.
Paola RizzoDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, Via Fossato di Mortara 64/B, 44121, Ferrara, Italy. rzzpla@unife.it.ORCID 0000-0001-7174-9674
Alberto CremonesiMaria Cecilia Hospital, GVM Care & Research, E.S. Health Science Foundation, Cotignola, Italy.
University of Ferrara · ITMaria Cecilia Hospital · ITLouisiana State University · USUniversity of Milan · ITHadassah Medical Center · ILIstituto Neurologico Mediterraneo · ITUniversity of Bologna · IT

Funding

Targeting y-secretase in GVHDP01CA166009 · NCI · UNIVERSITY OF MASSACHUSETTS AMHERST · PI OSBORNE, BARBARA A · 2013 to 2017
$4.9M
NCI NIH HHS P01 CA166009
6 · The paper itself

Abstract

backgroundThe lack of early diagnosis, progression markers and effective pharmacological treatment has dramatic unfavourable effects on clinical outcomes in patients with peripheral artery disease (PAD). Addressing these issues will require dissecting the molecular mechanisms underlying this disease. We sought to characterize the Notch signaling and atherosclerosis relevant markers in lesions from femoral arteries of symptomatic PAD patients.

methodsPlaque material from the common femoral, superficial femoral or popliteal arteries of 20 patients was removed by directional atherectomy. RNA was obtained from 9 out of 20 samples and analysed by quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR).

resultsWe detected expression of Notch ligands Delta-like 4 (Dll4) and Jagged1 (Jag1), of Notch target genes Hes1, Hey1, Hey2, HeyL and of markers of plaque inflammation and stability such as vascular cell adhesion molecule 1 (VCAM1), smooth muscle 22 (SM22), cyclooxygenase 2 (COX2), Bcl2, CD68 and miRNAs 21-5p, 125a-5p, 126-5p,146-5p, 155-5p, 424-5p. We found an "inflamed plaque" gene expression profile characterized by high Dll4 associated to medium/high CD68, COX2, VCAM1, Hes1, miR126-5p, miR146a-5p, miR155-5p, miR424-5p and low Jag1, SM22, Bcl2, Hey2, HeyL, miR125a-5p (2/9 patients) and a "stable plaque" profile characterized by high Jag1 associated to medium/high Hey2, HeyL, SM22, Bcl2, miR125a and low Dll4, CD68, COX2, VCAM1, miR126-5p, miR146a-5p, miR155-5p, miR424-5p (3/9 patients). The remaining patients (4/9) showed a plaque profile with intermediate characteristics.

conclusionsThis study reveals the existence of a gene signature associated to Notch activation by specific ligands that could be predictive of PAD progression.

Indexed as

TranscriptomeAdaptor Proteins, Signal TransducingAgedAnimalsCalcium-Binding ProteinsCholesterolFemaleFollow-Up StudiesHumansInflammationIntercellular Signaling Peptides and ProteinsJagged-1 ProteinLigandsMaleMicroRNAsMyocytes, Smooth MuscleAdaptor Proteins, Signal TransducingCalcium-Binding ProteinsCholesterolDLL4 protein, humanIntercellular Signaling Peptides and ProteinsJAG1 protein, humanJagged-1 ProteinLigandsMicroRNAsReceptors, NotchRNA, MessengerInflammationMacrophagesmicroRNANotchPeripheral artery diseaseVascular smooth muscle cells

Identifiers

PMID28472949
PMCPMC5418727
OpenAlexW2610663313

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.