Evidence map›Paper›PMID 20700110›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2010

POD nanoparticles expressing GDNF provide structural and functional rescue of light-induced retinal degeneration in an adult mouse.

Sarah P Read, Siobhan M Cashman, Rajendra Kumar-Singh

Open access · bronzeAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of 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
2.7field-weighted citation impact, top 10% 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, 60 citations in OpenAlex.

  1. Article
  2. Stem cell therapy in retinal diseases.Neural regeneration research · 2023
    Review
  3. Peptide cargo administration: current state and applications.Applied microbiology and biotechnology · 2023
    Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Corneal Penetrating Elastin-Like Polypeptide Carriers.Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics · 2016
    Article
  12. Article
  13. Article
  14. Article
  15. Vector platforms for gene therapy of inherited retinopathies.Progress in retinal and eye research · 2014
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

3 authors at 1 institution in 1 country.

Sarah P ReadDepartment of Ophthalmology, Tufts University School of Medicine, Boston, Massachusetts 02111, USA.
Siobhan M Cashman
Rajendra Kumar-Singh
Tufts University · US

Funding

Gene Therapy for Retinitis PigmentosaR01EY013837 · NEI · UNIVERSITY OF UTAH · PI KUMAR-SINGH, RAJENDRA · 2003 to 2012
$2.7M
Non-Viral Gene Therapy for Retinal DegenerationR01EY021805 · NEI · TUFTS UNIVERSITY BOSTON · PI KUMAR-SINGH, RAJENDRA · 2011 to 2014
$1.8M
VP22 AND TAT mediated gene therapy for the CNSR01EY014991 · NEI · UNIVERSITY OF UTAH · PI KUMAR-SINGH, RAJENDRA · 2004 to 2009
$1.4M
NEI NIH HHS EY013887NEI NIH HHS EY014991NEI NIH HHS R01 EY013837NEI NIH HHS R01 EY014991NEI NIH HHS R01 EY021805
6 · The paper itself

Abstract

Peptide for ocular delivery (POD) is a novel cationic cell-penetrating peptide (CPP) which, when conjugated with polyethylene glycol (PEG-POD), can deliver plasmid DNA to the retinal pigment epithelium (RPE) of adult murine retina. PEG-POD nanoparticles containing an expression cassette for glial cell line-derived neurotrophic factor (PEG-POD~GDNF) were investigated for their ability to inhibit light-induced photoreceptor apoptosis. PEG-POD~GDNF, control nanoparticles, or buffer were injected into the subretinal space of adult murine retina and retinal degeneration induced by blue light. Animals injected with PEG-POD~GDNF showed a significant reduction (3.9-7.7 fold) in apoptosis relative to control-injected animals. The thickness of the outer nuclear layer (ONL) of the superior retina of PEG-POD~GDNF-injected eyes was significantly greater (23.6-39.3%) than control-injected retina 14 days post-light treatment. PEG-POD~GDNF-injected eyes showed a 27-39% greater functional response relative to controls, as measured by electroretinogram (ERG) 7 days post-light treatment. This is one of only two studies demonstrating histological and functional rescue of a mouse model of retinal degeneration following nonviral administration of a transgene into adult retina. Although rescue is short lived for clinical application, this study represents an important step in the development of nonviral gene therapy for retinal diseases.

Indexed as

Genetic TherapyNanoparticlesAnimalsApoptosisCaspasesDrug Delivery SystemsElectroretinographyGlial Cell Line-Derived Neurotrophic FactorLightMiceMice, Inbred BALB CPeptide FragmentsPolyethylene GlycolsRadiation Injuries, ExperimentalRatsRetinaCaspasesGdnf protein, ratGlial Cell Line-Derived Neurotrophic FactorPeptide FragmentsPolyethylene Glycols

Identifiers

PMID20700110
PMCPMC2990513
OpenAlexW2108831584

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.