Evidence map›Paper›PMID 20393507›Full record

ArticleGene therapy2010

Increased perfusion and angiogenesis in a hindlimb ischemia model with plasmid FGF-2 delivered by noninvasive electroporation.

B Ferraro, Y L Cruz, M Baldwin, D Coppola, R Heller

Open access · greenAbstract readEvaluation Study
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 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.1field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Antioxidants (Basel, Switzerland) · 2021
    Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Vascular Regeneration in Peripheral Artery Disease.Arteriosclerosis, thrombosis, and vascular biology · 2020
    Review
  13. Article
  14. Article
  15. Review
  16. SNRK (Sucrose Nonfermenting 1-Related Kinase) Promotes Angiogenesis In Vivo.Arteriosclerosis, thrombosis, and vascular biology · 2018
    Article
  17. Article
  18. Article
  19. Article
  20. Skin electroporation of a plasmid encoding hCAP-18/LL-37 host defense peptide promotes wound healing.Molecular therapy : the journal of the American Society of Gene Therapy · 2014
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

B FerraroDepartment of Molecular Medicine, University of South Florida, Tampa, FL, USA.
Y L Cruz
M Baldwin
D Coppola
R Heller
University of South Florida · USMoffitt Cancer Center · USOld Dominion University · US

Funding

Electroporation System for Cutaneous Gene TransferR01EB005441 · NIBIB · UNIVERSITY OF SOUTH FLORIDA · PI HELLER, RICHARD · 2006 to 2009
$1.3M
NIBIB NIH HHS R01 EB005441
6 · The paper itself

Abstract

Gene therapy approaches delivering fibroblast growth factor-2 (FGF-2) have shown promise as a potential treatment for increasing blood flow to ischemic limbs. Currently, effective noninvasive techniques to deliver plasmids encoding genes of therapeutic interest, such as FGF-2, are limited. We sought to determine if intradermal injection of plasmid DNA encoding FGF-2 (pFGF) followed by noninvasive cutaneous electroporation (pFGFE+) could increase blood flow and angiogenesis in a rat model of hindlimb ischemia. pFGFE+ or control treatments were administered on postoperative day 0. Compared to injection of pFGF alone (pFGFE-), delivery of pFGFE+ significantly increased FGF-2 expression for 10 days. Further, the increase in FGF-2 expression with pFGFE+ was sufficient to significantly increase ischemic limb blood flow, measured by laser Doppler perfusion imaging, beginning on postoperative day 3. Ischemic limb blood flow in the pFGFE+ treatment group remained significantly higher than all control groups through the end point of the study, postoperative day 14. Immunohistochemical staining of gastrocnemius cross sections determined there was a twofold increase in capillary density in the pFGFE+ treatment group. Our results suggest that pFGFE+ is a potential noninvasive, nonviral therapeutic approach to increase perfusion and angiogenesis for the treatment of limb ischemia.

Indexed as

AnimalsDisease Models, AnimalElectroporationFibroblast Growth Factor 2Genetic TherapyGene Transfer TechniquesHindlimbIschemiaNeovascularization, PhysiologicPeripheral Vascular DiseasesRatsRegional Blood FlowFibroblast Growth Factor 2

Identifiers

PMID20393507
PMCPMC3138216
OpenAlexW1977531238

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.