Evidence map›Paper›PMID 24098781›Full record

ArticlePloS one2013

Attenuation of chondrogenic transformation in vascular smooth muscle by dietary quercetin in the MGP-deficient mouse model.

Kelly E Beazley, Florence Lima, Teresa Borras, Maria Nurminskaya

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Pathophysiology of Vascular Calcification.Current osteoporosis reports · 2015
    Review
  7. A review of the effect of diet on cardiovascular calcification.International journal of molecular sciences · 2015
    Review
  8. Wnt16 attenuates TGFβ-induced chondrogenic transformation in vascular smooth muscle.Arteriosclerosis, thrombosis, and vascular biology · 2015
    Article
  9. Article
  10. WNT16 primer.Differentiation; research in biological diversity
    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

4 authors at 2 institutions in 1 country.

Kelly E BeazleyDepartment of Biochemistry and Molecular Biology, School of Medicine, University of Maryland, Baltimore, Maryland, United States of America.
Florence Lima
Teresa Borras
Maria Nurminskaya
University of Maryland, Baltimore · USUniversity of North Carolina at Chapel Hill · US

Funding

Interdisciplinary Training Program Muscle BiologyT32AR007592 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI Aikaterini Kontrogianni-Konstantopoulos · 1996 to 2026
$11.7M
PRESSURE REGULATION OF HUMAN TRABECULAR MESHWORK GENESR01EY013126 · NEI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BORRAS, TERESA · 2000 to 2012
$4.1M
NEI NIH HHS EY13126NEI NIH HHS R01 EY013126NHLBI NIH HHS R01HL099305NIAMS NIH HHS T32 AR007592NIAMS NIH HHS T32AR007592
6 · The paper itself

Abstract

rationaleCartilaginous metaplasia of vascular smooth muscle (VSM) is characteristic for arterial calcification in diabetes and uremia and in the background of genetic alterations in matrix Gla protein (MGP). A better understanding of the molecular details of this process is critical for the development of novel therapeutic approaches to VSM transformation and arterial calcification.

objectiveThis study aimed to identify the effects of bioflavonoid quercetin on chondrogenic transformation and calcification of VSM in the MGP-null mouse model and upon TGF-β3 stimulation in vitro, and to characterize the associated alterations in cell signaling. METHODS AND

resultsMolecular analysis revealed activation of β-catenin signaling in cartilaginous metaplasia in Mgp-/- aortae in vivo and during chondrogenic transformation of VSMCs in vitro. Quercetin intercepted chondrogenic transformation of VSM and blocked activation of β-catenin both in vivo and in vitro. Although dietary quercetin drastically attenuated calcifying cartilaginous metaplasia in Mgp-/- animals, approximately one-half of total vascular calcium mineral remained as depositions along elastic lamellae.

conclusionQuercetin is potent in preventing VSM chondrogenic transformation caused by diverse stimuli. Combined with the demonstrated efficiency of dietary quercetin in preventing ectopic chondrogenesis in the MGP-null vasculature, these findings indicate a potentially broad therapeutic applicability of this safe for human consumption bioflavonoid in the therapy of cardiovascular conditions linked to cartilaginous metaplasia of VSM. Elastocalcinosis is a major component of MGP-null vascular disease and is controlled by a mechanism different from chondrogenic transformation of VSM and not sensitive to quercetin.

Indexed as

Animalsbeta CateninCalcium-Binding ProteinsChondrogenesisDNA PrimersExtracellular Matrix ProteinsImmunohistochemistryLuciferasesMatrix Gla ProteinMetaplasiaMiceMice, Inbred C57BLMice, KnockoutMuscle, Smooth, VascularQuercetinReal-Time Polymerase Chain Reactionbeta CateninCalcium-Binding ProteinsDNA PrimersExtracellular Matrix ProteinsLuciferasesMatrix Gla ProteinQuercetin

Identifiers

PMID24098781
PMCPMC3786963
OpenAlexW2058942818

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.