Evidence map›Paper›PMID 26200668›Full record

ArticleACS applied materials & interfaces2015

Lipopeptide-Coated Iron Oxide Nanoparticles as Potential Glycoconjugate-Based Synthetic Anticancer Vaccines.

Suttipun Sungsuwan, Zhaojun Yin, Xuefei Huang

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 2015. 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
2.1field-weighted citation impact, top 13% 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, 47 citations in OpenAlex.

  1. Review
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  7. Magnetic systems for cancer immunotherapy.Acta pharmaceutica Sinica. B · 2021
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  10. Nanoparticle cancer vaccines: Design considerations and recent advances.Asian journal of pharmaceutical sciences · 2020
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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

3 authors at 1 institution in 1 country.

Suttipun SungsuwanDepartment of Chemistry, Michigan State University, Chemistry Building, Room 426, 578 South Shaw Lane, East Lansing, Michigan 48824, United States.
Zhaojun YinDepartment of Chemistry, Michigan State University, Chemistry Building, Room 426, 578 South Shaw Lane, East Lansing, Michigan 48824, United States.
Xuefei HuangDepartment of Chemistry, Michigan State University, Chemistry Building, Room 426, 578 South Shaw Lane, East Lansing, Michigan 48824, United States.
Michigan State University · US

Funding

Virus-Like Particle Based Antigen Display as Multi-component Anticancer VaccinesR01CA149451 · NCI · MICHIGAN STATE UNIVERSITY · PI HUANG, XUEFEI · 2011 to 2015
$2.4M
NCI NIH HHS R01 CA149451NCI NIH HHS R01CA149451-01A1
6 · The paper itself

Abstract

Although iron oxide magnetic nanoparticles (NPs) have been widely utilized in molecular imaging and drug delivery studies, they have not been evaluated as carriers for glycoconjugate-based anticancer vaccines. Tumor-associated carbohydrate antigens (TACAs) are attractive targets for the development of anticancer vaccines. Due to the weak immunogenicity of these antigens, it is highly challenging to elicit strong anti-TACA immune responses. With their high biocompatibilities and large surface areas, magnetic NPs were synthesized for TACA delivery. The magnetic NPs were coated with phospholipid-functionalized TACA glycopeptides through hydrophobic-hydrophobic interactions without the need for any covalent linkages. Multiple copies of glycopeptides were presented on NPs, potentially leading to enhanced interactions with antibody-secreting B cells through multivalent binding. Mice immunized with the NPs generated strong antibody responses, and the glycopeptide structures important for high antibody titers were identified. The antibodies produced were capable of recognizing both mouse and human tumor cells expressing the glycopeptide, resulting in tumor cell death through complement-mediated cytotoxicities. These results demonstrate that magnetic NPs can be a new and simple platform for multivalently displaying TACA and boosting anti-TACA immune responses without the need for a typical protein carrier.

Indexed as

AnimalsAntibodiesAntigens, Tumor-Associated, CarbohydrateBiocompatible MaterialsCancer VaccinesComplement ActivationDendritic CellsDynamic Light ScatteringFerric CompoundsGlycoconjugatesGlycopeptidesHumansLipopeptidesMagnetite NanoparticlesMCF-7 CellsMiceAntibodiesAntigens, Tumor-Associated, CarbohydrateBiocompatible MaterialsCancer VaccinesFerric Compoundsferric oxideGlycoconjugatesGlycopeptidesLipopeptidesMagnetite NanoparticlesMucin-1Vaccines, Syntheticcancer vaccineglycopeptideimmunologymagnetic nanoparticlesMUC1

Identifiers

PMID26200668
PMCPMC4724168
OpenAlexW2275182145

What OpenQuestion holds

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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.