Evidence map›Paper›PMID 18990439›Full record

ArticleBiomaterials2009

A ligand-mediated nanovector for targeted gene delivery and transfection in cancer cells.

Omid Veiseh, Forrest M Kievit, Jonathan W Gunn, Buddy D Ratner, Miqin Zhang

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

50 citing papers in PubMed, 126 citations in OpenAlex.

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  20. Nanopharmacology in translational hematology and oncology.International journal of nanomedicine · 2014
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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

5 authors at 1 institution in 1 country.

Omid VeisehDepartment of Materials Science & Engineering, University of Washington, Seattle, WA 98195, USA.
Forrest M Kievit
Jonathan W Gunn
Buddy D Ratner
Miqin Zhang
University of Washington · US

Funding

Multifuctional Nanovector For Diagnosis And Treatment Of Pediatric Brain CancerR01EB006043 · NIBIB · UNIVERSITY OF WASHINGTON · PI ZHANG, MIQIN · 2007 to 2010
$1.6M
Nanovectors For Brain Tumor Diagnosis And TreatmentR01CA134213 · NCI · UNIVERSITY OF WASHINGTON · PI ZHANG, MIQIN · 2007 to 2011
$1.5M
Nanotechnology Platform for Pediatric Brain Cancer Imaging and TherapyR01CA119408 · NCI · UNIVERSITY OF WASHINGTON · PI ZHANG, MIQIN · 2005 to 2009
$1.4M
bHLH Factors in Medulloblastoma Genesis and MaintenanceR01CA112350 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI OLSON, JAMES M · 2005 to 2008
$1.3M
Training in Engineered BiomaterialsT32GM065098 · NIGMS · UNIVERSITY OF WASHINGTON · PI RATNER, BUDDY D · 2003 to 2007
$930k
NCI NIH HHS R01 CA112350NCI NIH HHS R01 CA119408NCI NIH HHS R01CA119408NCI NIH HHS R01CA134213NIBIB NIH HHS R01 EB006043NIBIB NIH HHS R01EB006043NIGMS NIH HHS T32GM065098
6 · The paper itself

Abstract

As conventional cancer therapies struggle with toxicity issues and irregular remedial efficacy, the preparation of novel gene therapy vectors could offer clinicians the tools for addressing the genetic errors of diseased tissue. The transfer of gene therapy to the clinic has proven difficult due to safety, target specificity, and transfection efficiency concerns. Polyethylenimine (PEI) nanoparticles have been identified as promising gene carriers that induce gene transfection with high efficiency. However, the inherent toxicity of the material and non-selective delivery are the major concerns in applying these particles clinically. Here, a non-viral nanovector has been developed by PEGylation of DNA-complexing PEI in nanoparticles functionalized with an Alexa Fluor 647 near infrared fluorophore, and the chlorotoxin (CTX) peptide which binds specifically to many forms of cancer. With this nanovector, the potential toxicity to healthy cells is minimized by both the reduction of the toxicity of PEI with the biocompatible copolymer and the targeted delivery of the nanovector to cancer cells, as evaluated by viability studies. The nanovector demonstrated high levels of targeting specificity and gene transfection efficiency with both C6 glioma and DAOY medulloblastoma tumor cells. Significantly, with the CTX as the targeting ligand, the nanovector may serve as a widely applicable gene delivery system for a broad array of cancer types.

Indexed as

Gene Transfer TechniquesTransfectionAnimalsCell Line, TumorCell SurvivalCyclic AMPElectrophoresis, Agar GelEndocytosisFlow CytometryGene Expression RegulationGenetic VectorsGreen Fluorescent ProteinsLigandsMagnetic Resonance SpectroscopyMiceNanostructures8-aminohexylamino cAMPChlorotoxinCyclic AMPGreen Fluorescent ProteinsLigandsPolyethylene GlycolsReceptors, Cell SurfaceScorpion Venoms

Identifiers

PMID18990439
PMCPMC2709815
OpenAlexW2004462960

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.