Evidence map›Paper›PMID 26368850›Full record

ArticleExperimental eye research2015

Topical application of a G-Quartet aptamer targeting nucleolin attenuates choroidal neovascularization in a model of age-related macular degeneration.

Derek Leaderer, Siobhan M Cashman, Rajendra Kumar-Singh

Open access · greenAbstract read
In one paragraph

Article in Experimental eye research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. Retinal Penetrating Adeno-Associated Virus.Investigative ophthalmology & visual science · 2024
    Article
  4. Article
  5. Aptamers' Potential to Fill Therapeutic and Diagnostic Gaps.Pharmaceuticals (Basel, Switzerland) · 2024
    Article
  6. Article
  7. Review
  8. Anti-nucleolin aptamer AS1411: an advancing therapeutic.Frontiers in molecular biosciences · 2023
    Review
  9. Review
  10. Article
  11. Review
  12. Inhibition of thyroid hormone receptor locally in the retina is a therapeutic strategy for retinal degeneration.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2017
    Article
  13. 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.

Derek LeadererDepartment of Developmental, Molecular and Chemical Biology, Program in Genetics, Sackler School of Graduate Biomedical Sciences, Tufts University School of Medicine, 136 Harrison Avenue, Boston, MA 02111, USA.
Siobhan M CashmanDepartment of Developmental, Molecular and Chemical Biology, Program in Genetics, Sackler School of Graduate Biomedical Sciences, Tufts University School of Medicine, 136 Harrison Avenue, Boston, MA 02111, USA.
Rajendra Kumar-SinghDepartment of Developmental, Molecular and Chemical Biology, Program in Genetics, Sackler School of Graduate Biomedical Sciences, Tufts University School of Medicine, 136 Harrison Avenue, Boston, MA 02111, USA. Electronic address: Rajendra.Kumar-Singh@tufts.edu.
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
NEI NIH HHS EY013837NEI NIH HHS EY021805NEI NIH HHS R01 EY013837NEI NIH HHS R01 EY021805
6 · The paper itself

Abstract

Choroidal neovascularization (CNV) associated with the 'wet' form of age related macular degeneration (AMD) is one of the most common causes of central vision loss among the elderly. The 'wet' form of AMD is currently treated by intravitreal delivery of anti-VEGF agents. However, intravitreal injections are associated with complications and long-term inhibition of VEGF leads to macular atrophy. Thus, there is currently an unmet need for the development of therapies for CNV that target molecules other than VEGF. Here, we describe nucleolin as a novel target for the 'wet' form of AMD. Nucleolin was found on the surface of endothelial cells that migrate from the choroid into the subretinal space in the laser-induced model of 'wet' AMD. AS1411 is a previously described G-quartet oligonucleotide that has been shown to bind nucleolin. We found that AS1411 inhibited the formation of tubes by human umbilical vein endothelial cells (HUVECs) by approximately 27.4% in vitro. AS1411 co-localized with the site of laser induced CNV in vivo. Intravitreally injected AS1411 inhibited laser-induced CNV by 37.6% and attenuated infiltration of macrophages by 40.3%. Finally, topical application of AS1411 led to a 43.4% reduction in CNV. Our observations have potential implications for the development of therapies for CNV and specifically for the 'wet' form of AMD.

Indexed as

Disease Models, AnimalAdministration, TopicalAnimalsAntigens, DifferentiationAptamers, NucleotideCell MovementChoroidal NeovascularizationEndothelium, VascularGlycosphingolipidsHuman Umbilical Vein Endothelial CellsIntravitreal InjectionsMacrophagesMiceMice, Inbred C57BLMicrovesselsNeovascularization, PathologicAGRO 100Antigens, DifferentiationAptamers, Nucleotideglycosphingolipid GSL-1Glycosphingolipidsmonocyte-macrophage differentiation antigenNucleolinOligodeoxyribonucleotidesPhosphoproteinsRNA-Binding ProteinsAge-related macular degeneration (AMD)AptamerAS1411Laser-induced choroidal neovascularization (CNV)Nucleolin

Identifiers

PMID26368850
PMCPMC4640196
OpenAlexW1630250478

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.