Evidence map›Paper›PMID 29302619›Full record

ArticleACS biomaterials science & engineering2017

Protein Mimetic and Anticancer Properties of Monocyte-Targeting Peptide Amphiphile Micelles.

Christopher Poon, Sampreeti Chowdhuri, Cheng-Hsiang Kuo, Yun Fang, Francis J Alenghat, Danielle Hyatt, Kian Kani, Mitchell E Gross, Eun Ji Chung

Open access · greenAbstract read
In one paragraph

Article in ACS biomaterials science & engineering, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.9field-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

16 citing papers in PubMed, 32 citations in OpenAlex.

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  10. CCR2-targeted micelles for anti-cancer peptide delivery and immune stimulation.Journal of controlled release : official journal of the Controlled Release Society · 2021
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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

9 authors at 2 institutions in 1 country.

Christopher PoonDepartment of Biomedical Engineering, University of Southern California, 1042 Downey Way, Los Angeles, California 90089, United States.
Sampreeti ChowdhuriDepartment of Biomedical Engineering, University of Southern California, 1042 Downey Way, Los Angeles, California 90089, United States.
Cheng-Hsiang KuoSection of Pulmonary and Critical Care, Department of Medicine, University of Chicago, 5841 South Maryland Avenue, Chicago, Illinois 60637, United States.
Yun FangSection of Pulmonary and Critical Care, Department of Medicine, University of Chicago, 5841 South Maryland Avenue, Chicago, Illinois 60637, United States.
Francis J AlenghatSection of Cardiology, Department of Medicine, University of Chicago, 5841 South Maryland Avenue, Chicago, Illinois 60637, United States.
Danielle HyattSection of Cardiology, Department of Medicine, University of Chicago, 5841 South Maryland Avenue, Chicago, Illinois 60637, United States.
Kian KaniLawrence J. Ellison Institute for Transformative Medicine of USC, Keck School of Medicine, University of Southern California, 2250 Alcazar Street, Los Angeles, California 90089, United States.
Mitchell E GrossLawrence J. Ellison Institute for Transformative Medicine of USC, Keck School of Medicine, University of Southern California, 2250 Alcazar Street, Los Angeles, California 90089, United States.
Eun Ji ChungDepartment of Biomedical Engineering, University of Southern California, 1042 Downey Way, Los Angeles, California 90089, United States.
University of Southern California · USUniversity of Chicago · US

Funding

Spatial Delivery of MicroRNA Inhibitor via Targeted Polyelectrolyte Complex Micelles to Treat Atherosclerosis.R01HL138223 · NHLBI · UNIVERSITY OF CHICAGO · PI FANG, YUN · 2017 to 2021
$2.0M
Multimodal Peptide Amphiphile Micelles for AtherosclerosisR00HL124279 · NHLBI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHUNG, EUN JI PAIGE · 2016 to 2018
$747k
Integrin-Triggered Signaling and Macrophage Mode Switching in AtherosclerosisK08HL116600 · NHLBI · UNIVERSITY OF CHICAGO · PI ALENGHAT, FRANCIS JOSEPH · 2013 to 2017
$655k
NHLBI NIH HHS K08 HL116600NHLBI NIH HHS R00 HL124279NHLBI NIH HHS R01 HL138223
6 · The paper itself

Abstract

Monocyte chemoattractant protein-1 (MCP-1) stimulates the migration of monocytes to inflammatory sites, leading to the progression of many diseases. Recently, we described a monocyte-targeting peptide amphiphile micelle (MCP-1 PAM) incorporated with the chemokine receptor CCR2 binding motif of MCP-1, which has a high affinity for monocytes in atherosclerotic plaques. We further report here the biomimetic components of MCP-1 PAMs and the influence of the nanoparticle upon binding to monocytes. We report that MCP-1 PAMs have enhanced secondary structure compared to the MCP-1 peptide. As a result, MCP-1 PAMs displayed improved binding and chemoattractant properties to monocytes, which upregulated the inflammatory signaling pathways responsible for monocyte migration. Interestingly, when MCP-1 PAMs were incubated in the presence of prostate cancer cells in vitro, the particle displayed anticancer efficacy by reducing CCR2 expression. Given that monocytes play an important role in tumor cell migration and invasion, our results demonstrate that PAMs can improve the native biofunctional properties of the peptide and may be used as an effective inhibitor to prevent chemokine-receptor interactions that promote disease progression.

Indexed as

atherosclerosismonocytenanoparticlepeptidepeptide amphiphile micelleprostate cancer

Identifiers

PMID29302619
PMCPMC5749269
OpenAlexW2757664723

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.