Evidence map›Paper›PMID 23117658›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2013

Transglutaminase inhibitors attenuate vascular calcification in a preclinical model.

Kelly E Beazley, Derek Banyard, Florence Lima, Stephanie C Deasey, Dmitry I Nurminsky, Mikhail Konoplyannikov, Maria V Nurminskaya

Open access · bronzeAbstract read
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
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  10. Article
  11. Wnt16 attenuates TGFβ-induced chondrogenic transformation in vascular smooth muscle.Arteriosclerosis, thrombosis, and vascular biology · 2015
    Article
  12. Article
  13. Inflammatory, metabolic, and genetic mechanisms of vascular calcification.Arteriosclerosis, thrombosis, and vascular biology · 2014
    Review
  14. Article
  15. Article
  16. Article
  17. 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

7 authors at 1 institution in 1 country.

Kelly E BeazleyDepartment of Biochemistry and Molecular Biology, University of Maryland, School of Medicine, 108 N Greene St, Baltimore, MD 21021, USA.
Derek Banyard
Florence Lima
Stephanie C Deasey
Dmitry I Nurminsky
Mikhail Konoplyannikov
Maria V Nurminskaya
University of Maryland, Baltimore · US

Funding

Interdisciplinary Training Program Muscle BiologyT32AR007592 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI Aikaterini Kontrogianni-Konstantopoulos · 1996 to 2026
$11.7M
Molecular mechanisms of medial calcification: regulation by transglutaminase 2R01HL093305 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI NURMINSKAYA, MARIA · 2009 to 2012
$1.3M
Regulation of osteoblast maturation by transglutaminasesR56DK071920 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI NURMINSKAYA, MARIA · 2010 to 2010
$225k
NHLBI NIH HHS R01 HL093305NHLBI NIH HHS R01HL093305NIAMS NIH HHS T32 AR007592NIAMS NIH HHS T32AR007592NIDDK NIH HHS 1R56DK71920NIDDK NIH HHS R56 DK071920
6 · The paper itself

Abstract

objectiveIn vitro, transglutaminase-2 (TG2)-mediated activation of the β-catenin signaling pathway is central in warfarin-induced calcification, warranting inquiry into the importance of this signaling axis as a target for preventive therapy of vascular calcification in vivo. METHODS AND

resultsThe adverse effects of warfarin-induced elastocalcinosis in a rat model include calcification of the aortic media, loss of the cellular component in the vessel wall, and isolated systolic hypertension, associated with accumulation and activation of TG2 and activation of β-catenin signaling. These effects of warfarin can be completely reversed by intraperitoneal administration of the TG2-specific inhibitor KCC-009 or dietary supplementation with the bioflavonoid quercetin, known to inhibit β-catenin signaling. Our study also uncovers a previously uncharacterized ability of quercetin to inhibit TG2. Quercetin reversed the warfarin-induced increase in systolic pressure, underlying the functional consequence of this treatment. Molecular analysis shows that quercetin diet stabilizes the phenotype of smooth muscle and prevents its transformation into osteoblastic cells.

conclusionsInhibition of the TG2/β-catenin signaling axis seems to prevent warfarin-induced elastocalcinosis and to control isolated systolic hypertension.

Indexed as

AnimalsAortaAortic Diseasesbeta CateninBlood PressureCell LineDisease Models, AnimalDose-Response Relationship, DrugEnzyme ActivationEnzyme InhibitorsGene Expression RegulationGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaGTP-Binding ProteinsIsoxazolesMalebeta CateninCtnnb1 protein, ratEnzyme InhibitorsGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaGTP-Binding ProteinsIsoxazolesKCC 009Protein Glutamine gamma Glutamyltransferase 2QuercetinTgm2 protein, ratTransglutaminasesWarfarin

Identifiers

PMID23117658
PMCPMC3544469
OpenAlexW2057246348

What OpenQuestion holds

Textmetadata
LicenceTDM
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.