Evidence map›Paper›PMID 23110920›Full record

ArticleMicrovascular research2013

Matrix Gla protein reinforces angiogenic resolution.

Bikram Sharma, Allan R Albig

Open access · greenAbstract read
In one paragraph

Article in Microvascular research, 2013. 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
1.2field-weighted citation impact, top 25% 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, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. BMP pathway suppression is an early event in inflammation-driven colon neoplasmatogenesis of uPA-deficient mice.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  14. Structural and functional insights into enzymes of the vitamin K cycle.Journal of thrombosis and haemostasis : JTH · 2016
    Review
  15. Article
  16. Article
  17. Conflicting forces of warfarin and matrix gla protein in the artery wall.Arteriosclerosis, thrombosis, and vascular biology · 2015
    Article
  18. Lumican exhibits anti-angiogenic activity in a context specific manner.Cancer microenvironment : official journal of the International Cancer Microenvironment Society · 2013
    Article
  19. Article
  20. 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

2 authors at 2 institutions in 1 country.

Bikram SharmaDepartment of Biology, Indiana State University, Terre Haute, IN 47809, USA.
Allan R Albig
Boise State University · USIndiana State University · US

Funding

Women's health: interplay of maternal diet and key demographics on neurological health in the rural frontier and remote WestP20GM103408 · NIGMS · UNIVERSITY OF IDAHO · PI Scott A Minnich · 2012 to 2026
$59.8M
UNDERGRADUATE COLLEGE OUTREACH PROGRAMP20RR016454 · NCRR · UNIVERSITY OF IDAHO · PI CHASE, JENNIFER R · 2001 to 2011
$35.3M
Identification and Characterization of an Integrin - Notch Signaling AxisR15GM102852 · NIGMS · BOISE STATE UNIVERSITY · PI ALBIG, ALLAN R · 2012 to 2017
$716k
Mechanisms by which MAGP-2 Promotes AngiogenesisR15CA133829 · NCI · INDIANA STATE UNIVERSITY · PI ALBIG, ALLAN R · 2009 to 2010
$284k
NCI NIH HHS 3R15CA133829-01A1S1NCI NIH HHS R15 CA133829NCRR NIH HHS P20 RR016454NIGMS NIH HHS P20 GM103408NIGMS NIH HHS R15 GM102852
6 · The paper itself

Abstract

Matrix Gla Protein (MGP) is an ECM molecule commonly associated with dysfunctions of large blood vessels such as arteriosclerosis and atherosclerosis. However, the exact role of MGP in the microvasculature is not clear. Utilizing a mouse MGP knockout model we found that MGP suppresses angiogenic sprouting from mouse aorta restricts microvascular density in cardiac and skeletal muscle, and is an endogenous inhibitor of tumor angiogenesis. Similarly, morpholino based knockdown of MGP in zebrafish embryos caused a progressive loss of luminal structures in intersegmental vessels, a phenotype reminiscent of Dll4/Notch inhibition. Accordingly, MGP suppressed Notch-dependent Hes-1 promoter activity and expression of Jagged1 mRNA relative to Dll4 mRNA. However, inhibition of BMP but not Notch or VEGF signaling reversed the excessive angiogenic sprouting phenotype of MGP knockout aortic rings suggesting that MGP may normally suppress angiogenic sprouting by blocking BMP signaling. Collectively, these results suggest that MGP is a multi-functional inhibitor of normal and abnormal angiogenesis that may function by coordinating with both Notch and BMP signaling pathways.

Indexed as

Neovascularization, PathologicAnimalsAortaCalcium-Binding ProteinsExtracellular Matrix ProteinsFemaleGene Expression Regulation, DevelopmentalImmunohistochemistryMatrix Gla ProteinMiceMice, Inbred C57BLMice, TransgenicMicrocirculationMuscle, SkeletalMyocardiumNeoplasmsCalcium-Binding ProteinsExtracellular Matrix ProteinsMatrix Gla ProteinReceptors, Notch

Identifiers

PMID23110920
PMCPMC3629274
OpenAlexW2011015107

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.