Evidence map›Paper›PMID 25156590›Full record

ArticleAdvanced healthcare materials2015

Monocyte-targeting supramolecular micellar assemblies: a molecular diagnostic tool for atherosclerosis.

Eun Ji Chung, Laurie B Mlinar, Kathryn Nord, Matthew J Sugimoto, Emily Wonder, Francis J Alenghat, Yun Fang, Matthew Tirrell

Abstract read
In one paragraph

Article in Advanced healthcare materials, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.9field-weighted citation impact, top 17% 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

30 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
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  8. Targeted polyelectrolyte complex micelles treat vascular complications in vivo.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  9. Review
  10. Article
  11. Article
  12. CCR2-targeted micelles for anti-cancer peptide delivery and immune stimulation.Journal of controlled release : official journal of the Controlled Release Society · 2021
    Article
  13. Article
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  15. Article
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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 1 institution in 1 country.

Eun Ji ChungInstitute for Molecular Engineering, University of Chicago, 5747 S. Ellis Ave, Chicago, IL, 60637, USA.
Laurie B Mlinar
Kathryn Nord
Matthew J Sugimoto
Emily Wonder
Francis J Alenghat
Yun Fang
Matthew Tirrell
University of Chicago · US

Funding

Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
miR-10a regulation of regional arterial endothelial phenotypes in atherosclerosisR00HL103789 · NHLBI · UNIVERSITY OF CHICAGO · PI FANG, YUN · 2013 to 2015
$729k
Integrin-Triggered Signaling and Macrophage Mode Switching in AtherosclerosisK08HL116600 · NHLBI · UNIVERSITY OF CHICAGO · PI ALENGHAT, FRANCIS JOSEPH · 2013 to 2017
$655k
NCATS NIH HHS UL1 TR000430NHLBI NIH HHS K08 HL116600NHLBI NIH HHS R00 HL103789
6 · The paper itself

Abstract

Atherosclerosis is a multifactorial inflammatory disease that can progress silently for decades and result in myocardial infarction, stroke, and death. Diagnostic imaging technologies have made great strides to define the degree of atherosclerotic plaque burden through the severity of arterial stenosis. However, current technologies cannot differentiate more lethal "vulnerable plaques," and are not sensitive enough for preventive medicine. Imaging early molecular markers and quantifying the extent of disease progression continues to be a major challenge in the field. To this end, monocyte-targeting, peptide amphiphile micelles (PAMs) are engineered through the incorporation of the chemokine receptor CCR2-binding motif of monocyte chemoattractant protein-1 (MCP-1) and MCP-1 PAMs are evaluated preclinically as diagnostic tools for atherosclerosis. Monocyte-targeting is desirable as the influx of monocytes is a marker of early lesions, accumulation of monocytes is linked to atherosclerosis progression, and rupture-prone plaques have higher numbers of monocytes. MCP-1 PAMs bind to monocytes in vitro, and MCP-1 PAMs detect and discriminate between early- and late-stage atherosclerotic aortas. Moreover, MCP-1 PAMs are found to be eliminated via renal clearance and the mononuclear phagocyte system (MPS) without adverse side effects. Thus, MCP-1 PAMs are a promising new class of diagnostic agents capable of monitoring the progression of atherosclerosis.

Indexed as

Amino Acid SequenceAnimalsApolipoproteins EAtherosclerosisBinding SitesChemokine CCL2Drug Evaluation, PreclinicalFemaleMacrophagesMicellesMice, TransgenicMolecular Sequence DataMonocytesPathology, MolecularReceptors, CCR2Recombinant ProteinsApolipoproteins ECcl2 protein, mouseCcr2 protein, mouseChemokine CCL2MicellesReceptors, CCR2Recombinant Proteinsatherosclerosismolecular imagingpeptide amphiphilesself-assemblytargeting

Identifiers

PMID25156590
PMCPMC4336846
OpenAlexW1970183428

What OpenQuestion holds

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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.