Evidence map›Paper›PMID 18063165›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2008

Efficient expression of vascular endothelial growth factor using minicircle DNA for angiogenic gene therapy.

Chien-Wen Chang, Lane V Christensen, Minhyung Lee, Sung Wan Kim

Open access · greenAbstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2008. 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
0.7field-weighted citation impact, top 31% 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, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Functional polymers of gene delivery for treatment of myocardial infarct.Journal of controlled release : official journal of the Controlled Release Society · 2014
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. New generation of plasmid backbones devoid of antibiotic resistance marker for gene therapy trials.Molecular therapy : the journal of the American Society of Gene Therapy · 2011
    Review
  15. Article
  16. Nanoparticles for retinal gene therapy.Progress in retinal and eye research · 2010
    Review
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.

Chien-Wen ChangDepartment of Pharmaceutics and Pharmaceutical Chemistry, University of Utah, Salt Lake City, UT 84112-5820, USA.
Lane V Christensen
Minhyung Lee
Sung Wan Kim
University of Utah · USHanyang University · KR

Funding

FUNCTIONAL AND TARGETING POLYMERIC GENE CARRIERSR01HL065477 · NHLBI · UNIVERSITY OF UTAH · PI KIM, SUNG WAN · 2000 to 2012
$4.3M
NHLBI NIH HHS HL 65477NHLBI NIH HHS R01 HL065477
6 · The paper itself

Abstract

The application of plasmid DNA (pDNA)-based gene therapy is limited by its inefficient transgene expression. In this study, minicircle DNA was evaluated for efficient vascular endothelial growth factor (VEGF) expression in skeletal muscle cells. Production of minicircle DNA encoding VEGF was studied by a semi-quantitative electrophoresis method leading to optimized bacterial culture conditions and producing high purity (86.6%) minicircle DNA. The VEGF minicircle DNA under control of the SV40 promoter (pMini-SV-VEGF) showed an increased amount of VEGF mRNA and up to 8 times more VEGF expression than a conventional plasmid (pSV-VEGF) in two different skeletal muscle cell lines (C2C12 and L8). Minicircle DNA with different promoters, including the SV40, CMV and chicken beta-actin, was tested for VEGF expression in a C2C12 skeletal muscle cell line. The high VEGF expression generated by minicircle DNA stimulated efficient endothelial cell growth in vitro. Furthermore, minicircle DNA expressed higher VEGF compared to conventional plasmid in the tibialis anterior (TA) muscle of mice. Taken together, the results suggest that minicircle DNA is an efficacious gene vector for angiogenic VEGF expression in skeletal muscle and may be useful for treating peripheral arterial disease (PAD).

Indexed as

AnimalsCell LineCell ProliferationCells, CulturedDNA, CircularEndothelial CellsGenetic TherapyHumansMaleMiceMice, Inbred BALB CMuscle, SkeletalNeovascularization, PhysiologicPlasmidsPromoter Regions, GeneticRatsDNA, CircularRNA, MessengerVascular Endothelial Growth Factor A

Identifiers

PMID18063165
PMCPMC2677388
OpenAlexW2067034097

What OpenQuestion holds

Textmetadata
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.