Evidence map›Paper›PMID 36054456›Full record

ArticleJournal of biomedical materials research. Part B, Applied biomaterials2023

In vitro assessment of varying peptide surface density on the suppression of angiogenesis by micelles displaying αvβ3 blocking peptides.

Neha Phani Bhushan, Trevor Stack, Evan A Scott, Kenneth R Shull, Benjamin Mathew, Divya Bijukumar

Open access · hybridAbstract read
In one paragraph

Article in Journal of biomedical materials research. Part B, Applied biomaterials, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 47% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

6 authors at 3 institutions in 1 country.

Neha Phani BhushanDepartment of Biomedical Sciences, University of Illinois College of Medicine at Rockford, Rockford, Illinois, USA.
Trevor StackDepartment of Biomedical Engineering, Northwestern University, Evanston, Illinois, USA.
Evan A ScottDepartment of Biomedical Engineering, Northwestern University, Evanston, Illinois, USA.ORCID 0000-0002-8945-2892
Kenneth R ShullDepartment of Biomedical Engineering, Northwestern University, Evanston, Illinois, USA.
Benjamin MathewDepartment of Ophthalmology and Visual Sciences, University of Illinois, Chicago, Illinois, USA.
Divya BijukumarDepartment of Biomedical Sciences, University of Illinois College of Medicine at Rockford, Rockford, Illinois, USA.ORCID 0000-0001-8114-5444
Northwestern University · USIllinois College · USUniversity of Illinois Urbana-Champaign · US

Funding

Valency and distance co-optimized peptide bound PEG-b-PPS Filomicelles hydrogel depot for anti-integrin therapeuticsR03EB032602 · NIBIB · UNIVERSITY OF ILLINOIS AT CHICAGO · PI BIJUKUMAR, DIVYA RANI · 2022 to 2023
$160k
NIBIB NIH HHS R03 EB032602
6 · The paper itself

Abstract

Ligand targeted therapy (LTT) is a precision medicine strategy that can selectively target diseased cells while minimizing off-target effects on healthy cells. Integrin-targeted LTT has been developed recently for angiogenesis-related diseases. However, the clinical success is based on the optimal design of the nanoparticles for inducing receptor clustering within the cell membrane. The current study focused on determining the surface density of Ser-Asp-Val containing anti-integrin heptapeptide on poly (ethylene glycol)-b-poly(propylene sulfide) micelles (MC) required for anti-angiogenic effects on HUVECs. Varying peptide density on PEG-b-PPS/Pep-PA MCs (Pep-PA-Peptide-palmitoleic acid) was used in comparison to a random peptide (SGV) and cRGD (cyclic-Arginine-Glycine-Aspartic acid) construct at 5%-density on MCs. Immunocytochemistry using CD51/CD31 antibody was performed to study the integrin blocking by MCs. In addition, the expression of VWF and PECAM-1, cell migration and tube formation was evaluated in the presence of PEG-b-PPS/Pep-PA MCs. The results show PEG-b-PPS/SDV-PA MCs with 5%-peptide density to achieve significantly higher αvβ3 blocking compared to random peptide as well as cRGD. In addition, αvβ3 blocking via MCs further reduced the expression of vWF and PECAM-1 angiogenesis protein expression in HUVECs. Although a significant level of integrin blocking was observed for 1%-peptide density on MCs, the cell migration and tube formation were not significantly affected. In conclusion, the results of this study demonstrate that the peptide surface density on PEG-b-PPS/Pep-PA MCs has a significant impact in integrin blocking as well as inhibiting angiogenesis during LTT. The outcomes of this study provides insight into the design of ligand targeted nanocarriers for various disease conditions.

Indexed as

Integrin alphaVbeta3MicellesLigandsPeptidesPolyethylene GlycolsSulfidesIntegrin alphaVbeta3LigandsMicellesPeptidesPolyethylene Glycolspoly(ethylene glycol)-stabilized poly(propylene sulfide)Sulfidesanti-angiogenic peptideLTTmicellesPEG-b-PPSαvβ3

Identifiers

PMID36054456
PMCPMC9771939
OpenAlexW4293590396

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.