Evidence map›Paper›PMID 26061296›Full record

ReviewJournal of drug targeting2015

Targeted polymeric nanoparticles for cancer gene therapy.

Jayoung Kim, David R Wilson, Camila G Zamboni, Jordan J Green

Abstract readReview
In one paragraph

Review in Journal of drug targeting, 2015. 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
2.9field-weighted citation impact, top 9% 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, 53 citations in OpenAlex.

  1. Review
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  9. Article
  10. Gene delivery nanoparticles to modulate angiogenesis.Advanced drug delivery reviews · 2017
    Review
  11. A Triple-Fluorophore-Labeled Nucleic Acid pH Nanosensor to Investigate Non-viral Gene Delivery.Molecular therapy : the journal of the American Society of Gene Therapy · 2017
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. 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

4 authors at 2 institutions in 2 countries.

Jayoung Kima Department of Biomedical Engineering and the Translational Tissue Engineering Center , Johns Hopkins University School of Medicine , Baltimore , MD , USA .
David R Wilsona Department of Biomedical Engineering and the Translational Tissue Engineering Center , Johns Hopkins University School of Medicine , Baltimore , MD , USA .
Camila G Zambonia Department of Biomedical Engineering and the Translational Tissue Engineering Center , Johns Hopkins University School of Medicine , Baltimore , MD , USA .
Jordan J Greena Department of Biomedical Engineering and the Translational Tissue Engineering Center , Johns Hopkins University School of Medicine , Baltimore , MD , USA .
Johns Hopkins Medicine · USJohns Hopkins University · US

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI WILLIAM George NELSON · 1985 to 2026
$208.6M
BIOMEDICAL ENGINEERING TRAINING PROGRAMT32GM007057 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI KANOLD, PATRICK O, KARCHIN, RACHEL · 1985 to 2023
$10.4M
Gene Delivery Nanoparticles to Treat GlioblastomaR01EB016721 · NIBIB · JOHNS HOPKINS UNIVERSITY · PI GREEN, JORDAN · 2013 to 2017
$1.9M
NCI NIH HHS P30 CA006973NIBIB NIH HHS 1R01EB016721NIBIB NIH HHS R01 EB016721NIGMS NIH HHS T32 GM007057
6 · The paper itself

Abstract

In this article, advances in designing polymeric nanoparticles for targeted cancer gene therapy are reviewed. Characterization and evaluation of biomaterials, targeting ligands, and transcriptional elements are each discussed. Advances in biomaterials have driven improvements to nanoparticle stability and tissue targeting, conjugation of ligands to the surface of polymeric nanoparticles enable binding to specific cancer cells, and the design of transcriptional elements has enabled selective DNA expression specific to the cancer cells. Together, these features have improved the performance of polymeric nanoparticles as targeted non-viral gene delivery vectors to treat cancer. As polymeric nanoparticles can be designed to be biodegradable, non-toxic, and to have reduced immunogenicity and tumorigenicity compared to viral platforms, they have significant potential for clinical use. Results of polymeric gene therapy in clinical trials and future directions for the engineering of nanoparticle systems for targeted cancer gene therapy are also presented.

Indexed as

NanoparticlesAnimalsBiocompatible MaterialsGene Expression Regulation, NeoplasticGenetic TherapyGenetic VectorsGene Transfer TechniquesHumansNeoplasmsPolymersBiocompatible MaterialsPolymersCancer therapycell-specificitygene deliverynanoparticlespolymeric biomaterialpromotertargeting ligandstissue-specificity

Identifiers

PMID26061296
PMCPMC4696040
OpenAlexW1923342667

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.