Evidence map›Paper›PMID 27694328›Full record

ArticleJournal of the American Heart Association2016

Novel Role for Matrix Metalloproteinase 9 in Modulation of Cholesterol Metabolism.

Samuel Hernandez-Anzaldo, Vesna Brglez, Bianca Hemmeryckx, Dickson Leung, Janos G Filep, Jean E Vance, Dennis E Vance, Zamaneh Kassiri, Roger H Lijnen, Gérard Lambeau and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

23 citing papers in PubMed, 35 citations in OpenAlex.

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  19. Metabolic Drivers of Invasion in Glioblastoma.Frontiers in cell and developmental biology · 2021
    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

11 authors at 5 institutions in 3 countries.

Samuel Hernandez-AnzaldoDepartment of Biochemistry, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada.
Vesna BrglezInstitut de Pharmacologie Moléculaire et Cellulaire, Centre National de la Recherche Scientifique, Université Côte d'Azur, Nice, France.
Bianca HemmeryckxDepartment of Cardiovascular Sciences, Center for Molecular and Vascular Biology, KU Leuven, Leuven, Belgium.
Dickson LeungDepartment of Biochemistry, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada.
Janos G FilepThe Maisonneuve-Rosemont Hospital Research Centre, University of Montreal, Canada.
Jean E VanceDepartment of Medicine, Cardiovascular Research Group, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada.
Dennis E VanceDepartment of Biochemistry, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada.
Zamaneh KassiriDepartment of Physiology, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada Mazankowski Alberta Heart Institute, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada.
Roger H LijnenDepartment of Cardiovascular Sciences, Center for Molecular and Vascular Biology, KU Leuven, Leuven, Belgium cf2@ualberta.ca roger.lijnen@med.kuleuven.be.
Gérard LambeauInstitut de Pharmacologie Moléculaire et Cellulaire, Centre National de la Recherche Scientifique, Université Côte d'Azur, Nice, France.
Carlos Fernandez-PatronDepartment of Biochemistry, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada Mazankowski Alberta Heart Institute, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada cf2@ualberta.ca roger.lijnen@med.kuleuven.be.
University of Alberta · CAKU Leuven · BEHôpital Maisonneuve-Rosemont · CAInstitut de Pharmacologie Moléculaire et Cellulaire · FRUniversité Côte d'Azur · FR

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

backgroundThe development of atherosclerosis is strongly linked to disorders of cholesterol metabolism. Matrix metalloproteinases (MMPs) are dysregulated in patients and animal models with atherosclerosis. Whether systemic MMP activity influences cholesterol metabolism is unknown. METHODS AND

resultsWe examined MMP-9-deficient (Mmp9

conclusionsOur results show that MMP-9 modulates cholesterol metabolism, at least in part, through a novel MMP-9-plasma secreted phospholipase A

Indexed as

AcetatesAnimalsCholestanetriol 26-MonooxygenaseCholesterolCholesterol 7-alpha-HydroxylaseGene Expression RegulationIndolesIntestinal AbsorptionKeto AcidsLipid MetabolismLiverMaleMatrix Metalloproteinase 9MiceMice, KnockoutPhospholipase A2 InhibitorsAcetatesCholestanetriol 26-MonooxygenaseCholesterolCholesterol 7-alpha-HydroxylaseCyp27a1 protein, mouseCyp7a1 protein, mouseIndolesKeto AcidsMatrix Metalloproteinase 9Mmp9 protein, mousePhospholipase A2 InhibitorsPhospholipases A2Srebf2 protein, mouseSterol Regulatory Element Binding Protein 2varespladibatherosclerosischolesterollipid metabolismlivermatrix metalloproteinaseplasma phospholipase A2

Identifiers

PMID27694328
PMCPMC5121519
OpenAlexW2526592245

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.