Evidence map›Paper›PMID 29424479›Full record

ArticleJournal of biomedical materials research. Part A2018

Biomimetic peptide display from a polymeric nanoparticle surface for targeting and antitumor activity to human triple-negative breast cancer cells.

Eric M Bressler, Jayoung Kim, Ron B Shmueli, Adam C Mirando, Hojjat Bazzazi, Esak Lee, Aleksander S Popel, Niranjan B Pandey, Jordan J Green

Open access · greenAbstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

21 citing papers in PubMed, 46 citations in OpenAlex.

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  14. Theranostics for Triple-Negative Breast Cancer.Diagnostics (Basel, Switzerland) · 2023
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  18. Comprehensive comparison of theranostic nanoparticles in breast cancer.American journal of clinical and experimental immunology · 2022
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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 4 institutions in 1 country.

Eric M BresslerAsclepiX Therapeutics, Baltimore, Maryland, 21218.
Jayoung KimDepartment of Biomedical Engineering and Institute for NanoBioTechnology, Johns Hopkins School of Medicine, Baltimore, Maryland, 21231.
Ron B ShmueliAsclepiX Therapeutics, Baltimore, Maryland, 21218.
Adam C MirandoDepartment of Biomedical Engineering and Institute for NanoBioTechnology, Johns Hopkins School of Medicine, Baltimore, Maryland, 21231.
Hojjat BazzaziDepartment of Biomedical Engineering and Institute for NanoBioTechnology, Johns Hopkins School of Medicine, Baltimore, Maryland, 21231.
Esak LeeDepartment of Biomedical Engineering and Institute for NanoBioTechnology, Johns Hopkins School of Medicine, Baltimore, Maryland, 21231.
Aleksander S PopelAsclepiX Therapeutics, Baltimore, Maryland, 21218.
Niranjan B PandeyAsclepiX Therapeutics, Baltimore, Maryland, 21218.
Jordan J GreenAsclepiX Therapeutics, Baltimore, Maryland, 21218.
Johns Hopkins University · USSidney Kimmel Comprehensive Cancer Center · USAsclepiX Therapeutics (United States) · USJohns Hopkins Medicine · US

Funding

Wilmer Core Grant for Vision ResearchP30EY001765 · NEI · JOHNS HOPKINS UNIVERSITY · PI Jiang Qian · 1985 to 2026
$22.1M
Cancer-specific nanoparticle-mediated gene therapy to treat hepatocellular carcinomaR01EB022148 · NIBIB · JOHNS HOPKINS UNIVERSITY · PI GREEN, JORDAN · 2016 to 2019
$1.5M
Nanoparticle-mediated peptide delivery for breast cancerR21CA152473 · NCI · JOHNS HOPKINS UNIVERSITY · PI GREEN, JORDAN · 2011 to 2012
$392k
Targeted nanoparticles to deliver a multimodal peptide to head and neck tumorsU43CA179506 · NCI · ASCLEPIX THERAPEUTICS, INC. · PI PANDEY, NIRANJAN B · 2014 to 2014
$258k
NCI NIH HHS R21 CA152473NCI NIH HHS U43 CA179506NEI NIH HHS P30 EY001765NIBIB NIH HHS R01 EB022148
6 · The paper itself

Abstract

While poly(lactic-co-glycolic acid)-block-polyethylene glycol (PLGA-PEG) nanoparticles (NPs) can encapsulate drug cargos and prolong circulation times, they show nonspecific accumulation in off-target tissues. Targeted delivery of drugs to tumor tissue and tumor vasculature is a promising approach for treating solid tumors while enhancing specificity and reducing systemic toxicity. AXT050, a collagen-IV derived peptide with both antitumor and antiangiogenic properties, is shown to bind to tumor-associated integrins with high affinity, which leads to targeted accumulation in tumor tissue. AXT050 conjugated to PLGA-PEG NPs at precisely controlled surface density functions both as a targeting agent to human tumor cells and demonstrates potential for simultaneous antitumorigenic and antiangiogenic activity. These targeted NPs cause inhibition of adhesion and proliferation in vitro when added to human triple-negative breast cancer cells and microvascular endothelial cells through binding to integrin α

Indexed as

Drug Delivery SystemsAngiogenesis InhibitorsAnimalsAntineoplastic AgentsCell Line, TumorFemaleHumansMice, NudeNanoconjugatesNanoparticlesPeptidesPolyestersPolyethylene GlycolsTissue DistributionTriple Negative Breast NeoplasmsAngiogenesis InhibitorsAntineoplastic AgentsNanoconjugatesPeptidesPolyesterspolyethylene glycol-poly(lactide-co-glycolide)Polyethylene Glycolscancerdrug deliverynanoparticlepeptidetargeting

Identifiers

PMID29424479
PMCPMC6035748
OpenAlexW2793021652

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.