Evidence map›Paper›PMID 21638084›Full record

ArticleMolecular imaging and biology2012

RGD-conjugated human ferritin nanoparticles for imaging vascular inflammation and angiogenesis in experimental carotid and aortic disease.

Toshiro Kitagawa, Hisanori Kosuge, Masaki Uchida, Monica M Dua, Yasunori Iida, Ronald L Dalman, Trevor Douglas, Michael V McConnell

Abstract read
In one paragraph

Article in Molecular imaging and biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

27 citing papers in PubMed, 62 citations in OpenAlex.

  1. Review
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  3. Article
  4. Review
  5. Review
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  8. Review
  9. Ferritin expression in the periodontal tissues of primates.European journal of histochemistry : EJH · 2019
    Article
  10. Ferritin-based drug delivery systems: Hybrid nanocarriers for vascular immunotargeting.Journal of controlled release : official journal of the Controlled Release Society · 2018
    Review
  11. Article
  12. Functional ferritin nanoparticles for biomedical applications.Frontiers of chemical science and engineering · 2017
    Article
  13. Article
  14. Review
  15. Dual-Modality Activity-Based Probes as Molecular Imaging Agents for Vascular Inflammation.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2016
    Article
  16. Article
  17. Article
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  19. 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

8 authors at 2 institutions in 1 country.

Toshiro KitagawaDivision of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA 94305-5233, USA.
Hisanori Kosuge
Masaki Uchida
Monica M Dua
Yasunori Iida
Ronald L Dalman
Trevor Douglas
Michael V McConnell
Stanford University · USMontana State University · US

Funding

Signature Protein Profiles to Identify AAAsP50HL083800 · NHLBI · STANFORD UNIVERSITY · PI DALMAN, RONALD L · 2006 to 2010
$13.7M
Multi-modality Cellular Imaging of Vascular InflammationR01HL078678 · NHLBI · STANFORD UNIVERSITY · PI MCCONNELL, MICHAEL V · 2004 to 2007
$1.6M
Targeted MRI with Protein Cage Architectures (RMI)R21EB005364 · NIBIB · MONTANA STATE UNIVERSITY - BOZEMAN · PI DOUGLAS, TREVOR · 2005 to 2008
$1.4M
NHLBI NIH HHS P50 HL083800NHLBI NIH HHS R01 HL078678NIBIB NIH HHS R21 EB005364
6 · The paper itself

Abstract

purposeInflammation and angiogenesis are important contributors to vascular disease. We evaluated imaging both of these biological processes, using Arg-Gly-Asp (RGD)-conjugated human ferritin nanoparticles (HFn), in experimental carotid and abdominal aortic aneurysm (AAA) disease. PROCEDURES: Macrophage-rich carotid lesions were induced by ligation in hyperlipidemic and diabetic FVB mice (n = 16). AAAs were induced by angiotensin II infusion in apoE(-/-) mice (n=10). HFn, with or without RGD peptide, was labeled with Cy5.5 and injected intravenously for near-infrared fluorescence imaging.

resultsRGD-HFn showed significantly higher signal than HFn in diseased carotids and AAAs relative to non-diseased regions, both in situ (carotid: 1.88 ± 0.30 vs. 1.17 ± 0.10, p = 0.04; AAA: 2.59 ± 0.24 vs. 1.82 ± 0.16, p = 0.03) and ex vivo. Histology showed RGD-HFn colocalized with macrophages in carotids and both macrophages and neoangiogenesis in AAA lesions.

conclusionsRGD-HFn enhances vascular molecular imaging by targeting both vascular inflammation and angiogenesis, and allows more comprehensive detection of high-risk atherosclerotic and aneurysmal vascular diseases.

Indexed as

FerritinsNanoparticlesOligopeptidesAnimalsAortic DiseasesCarotid ArteriesCarotid Artery DiseasesCattleCells, CulturedDiagnostic Techniques, CardiovascularDisease Models, AnimalEndothelial CellsHumansImmunohistochemistryInflammationMacrophagesarginyl-glycyl-aspartic acidFerritinsOligopeptides

Identifiers

PMID21638084
PMCPMC3963502
OpenAlexW1970092868

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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.