Evidence map›Paper›PMID 25503692›Full record

ArticleGene therapy2015

Inhibition of choroidal fibrovascular membrane formation by new class of RNA interference therapeutic agent targeting periostin.

T Nakama, S Yoshida, K Ishikawa, Y Kobayashi, Y Zhou, S Nakao, Y Sassa, Y Oshima, K Takao, A Shimahara and 10 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Gene therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.4field-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

23 citing papers in PubMed, 41 citations in OpenAlex.

  1. Collagen-producing eye cell atlas reveals distinct fibroblast fates in early injury vs. fibrotic subretinal disease.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Increased expression of periostin and tenascin-C in eyes with neovascular glaucoma secondary to PDR.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2020
    Article
  10. Review
  11. Article
  12. Article
  13. Periostin function in communication with extracellular matrices.Journal of cell communication and signaling · 2018
    Review
  14. Periostin in vitreoretinal diseases.Cellular and molecular life sciences : CMLS · 2017
    Review
  15. Review
  16. Periostin in kidney diseases.Cellular and molecular life sciences : CMLS · 2017
    Review
  17. Article
  18. Article
  19. Article
  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

20 authors at 6 institutions in 1 country.

T NakamaDepartment of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
S YoshidaDepartment of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
K IshikawaDepartment of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
Y KobayashiDepartment of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
Y ZhouDepartment of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
S NakaoDepartment of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
Y Sassa1] Department of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan [2] Department of Ophthalmology, Fukuoka University Chikushi Hospital, Fukuoka, Japan.ORCID 0000000237825351
Y OshimaDepartment of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
K TakaoAQUA Therapeutics Co., Ltd., Kobe, Japan.
A ShimaharaAQUA Therapeutics Co., Ltd., Kobe, Japan.
K YoshikawaAQUA Therapeutics Co., Ltd., Kobe, Japan.ORCID 0000000306058169
T HamasakiStrategic Headquarters for Research and Development, BONAC Corporation, BIO Factory, Fukuoka, Japan.
T OhgiStrategic Headquarters for Research and Development, BONAC Corporation, BIO Factory, Fukuoka, Japan.
H HayashiStrategic Headquarters for Research and Development, BONAC Corporation, BIO Factory, Fukuoka, Japan.
A MatsudaDepartment of Ophthalmology, Juntendo University School of Medicine, Tokyo, Japan.
A KudoDepartment of Biological Information, Tokyo Institute of Technology, Yokohama, Japan.
M NozakiDepartment of Ophthalmology and Visual Science, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Y OguraDepartment of Ophthalmology and Visual Science, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
M KurodaDepartment of Molecular Pathology, Tokyo Medical University, Tokyo, Japan.
T IshibashiDepartment of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
Kyushu University · JPBridge Of Nucleic Acids Chemistry (Japan) · JPNagoya City University · JPJuntendo University · JPTokyo Institute of Technology · JPTokyo Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Age-related macular degeneration (AMD) is a vision-threatening disease characterized by choroidal fibrovascular membrane (FVM) formation, choroidal neovascularization (CNV) and choroidal fibrosis. No safe and effective therapeutic method has been developed for the choroidal fibrosis, although anti-vascular endothelial growth factor therapy can partially shrink the CNV. We recently reported that periostin (POSTN), which is produced by retinal pigment epithelial cells, has an important role in the formation of preretinal FVMs, but its role in choroidal FVMs has not been determined. In this study, we used Postn knockout mice to investigate the role played by POSTN in choroidal FVM formation. In addition, we used a new class of RNA interference (RNAi) agent (NK0144) that targets POSTN and determined its effect on choroidal FVM development. Genetic ablation of Postn had an inhibitory effect not only on CNV formation but also on choroidal fibrosis in a mouse CNV model. NK0144 also had a greater inhibitory effect on both the CNV and choroidal fibrosis than control RNAi with no apparent adverse effects. These findings suggest a causal relationship between POSTN and choroidal FVM formation, and also a potential therapeutic role of intravitreal NK0144 for AMD.

Indexed as

RNA InterferenceAnimalsBase SequenceCell AdhesionCell Adhesion MoleculesCell MovementCell ProliferationCells, CulturedChoroidChoroidal NeovascularizationGene Knockdown TechniquesGenetic TherapyHumansIntravitreal InjectionsMacular DegenerationMice, Inbred C57BLCell Adhesion MoleculesPOSTN protein, humanRNA, Small InterferingTLR3 protein, mouseToll-Like Receptor 3

Identifiers

PMID25503692
OpenAlexW1973288416

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.