Evidence map›Paper›PMID 29563538›Full record

ArticleScientific reports2018

Ucma/GRP inhibits phosphate-induced vascular smooth muscle cell calcification via SMAD-dependent BMP signalling.

Brecht A Willems, Malgorzata Furmanik, Marjolein M J Caron, Martijn L L Chatrou, Dennis H M Kusters, Tim J M Welting, Michael Stock, Marta S Rafael, Carla S B Viegas, Dina C Simes and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

42 citing papers in PubMed, 58 citations in OpenAlex.

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  12. Roles of vitamin K‑dependent protein in biomineralization (Review).International journal of molecular medicine · 2024
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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

13 authors at 3 institutions in 3 countries.

Brecht A WillemsDepartment of Biochemistry, School for Cardiovascular Diseases, Maastricht University, Maastricht, The Netherlands.
Malgorzata FurmanikDepartment of Biochemistry, School for Cardiovascular Diseases, Maastricht University, Maastricht, The Netherlands.
Marjolein M J CaronDepartment of Orthopedic Surgery, School for Public Health and Primary Care, Maastricht University, Maastricht, The Netherlands.ORCID 0000-0001-5316-9211
Martijn L L ChatrouDepartment of Biochemistry, School for Cardiovascular Diseases, Maastricht University, Maastricht, The Netherlands.
Dennis H M KustersDepartment of Biochemistry, School for Cardiovascular Diseases, Maastricht University, Maastricht, The Netherlands.
Tim J M WeltingDepartment of Orthopedic Surgery, School for Public Health and Primary Care, Maastricht University, Maastricht, The Netherlands.
Michael StockDepartment of Experimental Medicine I, Nikolaus-Fiebiger Centre of Molecular Medicine, University of Erlangen, Nuremberg, Germany.
Marta S RafaelCentre of Marine Sciences (CCMAR), University of Algarve, Faro, Portugal.
Carla S B ViegasCentre of Marine Sciences (CCMAR), University of Algarve, Faro, Portugal.
Dina C SimesCentre of Marine Sciences (CCMAR), University of Algarve, Faro, Portugal.
Cees VermeerVitaK BV, Maastricht University, Maastricht, The Netherlands.
Chris P M ReutelingspergerDepartment of Biochemistry, School for Cardiovascular Diseases, Maastricht University, Maastricht, The Netherlands.ORCID 0000-0002-2334-9403
Leon J SchurgersDepartment of Biochemistry, School for Cardiovascular Diseases, Maastricht University, Maastricht, The Netherlands. l.schurgers@maastrichtuniversity.nl.
Maastricht University · NLUniversity of Algarve · PTFriedrich-Alexander-Universität Erlangen-Nürnberg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vascular calcification (VC) is the process of deposition of calcium phosphate crystals in the blood vessel wall, with a central role for vascular smooth muscle cells (VSMCs). VC is highly prevalent in chronic kidney disease (CKD) patients and thought, in part, to be induced by phosphate imbalance. The molecular mechanisms that regulate VC are not fully known. Here we propose a novel role for the mineralisation regulator Ucma/GRP (Upper zone of growth plate and Cartilage Matrix Associated protein/Gla Rich Protein) in phosphate-induced VSMC calcification. We show that Ucma/GRP is present in calcified atherosclerotic plaques and highly expressed in calcifying VSMCs in vitro. VSMCs from Ucma/GRP

Indexed as

AnimalsAortaAtherosclerosisBiomarkersBone Morphogenetic Protein 2Cells, CulturedChondrogenesisDisease Models, AnimalExtracellular Matrix ProteinsGene Expression RegulationHumansIntracellular Signaling Peptides and ProteinsMiceMice, Inbred C57BLMice, Knockout, ApoEMuscle, Smooth, VascularBiomarkersBmp2 protein, mouseBone Morphogenetic Protein 2dorsomorphinExtracellular Matrix ProteinsIntracellular Signaling Peptides and ProteinsPhosphatesProteinsPyrazolesPyrimidinesSmad ProteinsUcma protein, mouse

Identifiers

PMID29563538
PMCPMC5862840
OpenAlexW2806544996

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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.