Evidence map›Paper›PMID 20463761›Full record

ArticleGene therapy2010

A combinatorial approach for targeted delivery using small molecules and reversible masking to bypass nonspecific uptake in vivo.

Q Shi, A T Nguyen, Y Angell, D Deng, C-R Na, K Burgess, D D Roberts, F C Brunicardi, N S Templeton

Open access · greenAbstract read
In one paragraph

Article in Gene therapy, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Novel Small Molecule Probes for Metastatic Melanoma.ACS medicinal chemistry letters · 2017
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. RNA interference and cancer therapy.Pharmaceutical research · 2011
    Review
  10. Article
  11. 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

9 authors at 3 institutions in 1 country.

Q ShiDepartment of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX, USA.
A T Nguyen
Y Angell
D Deng
C-R Na
K Burgess
D D Roberts
F C Brunicardi
N S Templeton
Baylor College of Medicine · USTexas A&M University · USNational Institutes of Health · US

Funding

Roles of Glycoconjugates and Redox Signaling in Tumor BiologyZIASC009174 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI ROBERTS, DAVID D · 2009 to 2024
$4.9M
Design and Synthesis of Functional NGF PeptidomimeticsR01MH070040 · NIMH · TEXAS A&M UNIVERSITY SYSTEM · PI BURGESS, KEVIN · 2005 to 2009
$1.9M
Evolving Libraries of Bivalent Compounds (RMI)P41GM076261 · NIGMS · TEXAS A&M UNIVERSITY SYSTEM · PI BURGESS, KEVIN · 2005 to 2007
$1.0M
Intramural NIH HHSNIGMS NIH HHS GM076261NIGMS NIH HHS P41 GM076261NIMH NIH HHS MH070040NIMH NIH HHS R01 MH070040
6 · The paper itself

Abstract

We have developed a multi-disciplinary approach combining molecular biology, delivery technology, combinatorial chemistry and reversible masking to create improved systemic, targeted delivery of plasmid DNA while avoiding nonspecific uptake in vivo. We initially used a well-characterized model targeting the asialolglycoprotein receptor in the liver. Using our bilamellar invaginated vesicle (BIV) liposomal delivery system with reversible masking, we increased expression in the liver by 76-fold, nearly equaling expression in first-pass organs using non-targeted complexes, with no expression in other organs. The same technology was then applied to efficiently target delivery to a human tumor microenvironment model. We achieved efficient, targeted delivery by attachment of specific targeting ligands to the surface of our BIV complexes in conjunction with reversible masking to bypass nonspecific tissues and organs. We identified ligands that target a human tumor microenvironment created in vitro by co-culturing primary human endothelial cells with human lung or pancreatic cancer cells. The model was confirmed by increased expression of tumor endothelial phenotypes including CD31 and vascular endothelial growth factor-A, and prolonged survival of endothelial capillary-like structures. The co-cultures were used for high-throughput screening of a specialized small molecule library to identify ligands specific for human tumor-associated endothelial cells in vitro. We identified small molecules that enhanced the transfection efficiency of tumor-associated endothelial cells, but not normal human endothelial cells or cancer cells. Intravenous (i.v.) injection of our targeted, reversibly masked complexes into mice, bearing human pancreatic tumor and endothelial cells, specifically increased transfection to this tumor microenvironment approximately 200-fold. Efficacy studies using our optimized targeted delivery of a plasmid encoding thrombospondin-1 eliminated tumors completely after five i.v. injections administered once every week.

Indexed as

TransfectionAnimalsAsialoglycoprotein ReceptorCell Line, TumorCells, CulturedCoculture TechniquesEndothelial CellsGenetic TherapyHumansLiposomesMiceNeoplasmsPlasmidsPlatelet Endothelial Cell Adhesion Molecule-1Vascular Endothelial Growth Factor AAsialoglycoprotein ReceptorLiposomesPlatelet Endothelial Cell Adhesion Molecule-1Vascular Endothelial Growth Factor A

Identifiers

PMID20463761
PMCPMC2923228
OpenAlexW2090075065

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.