Evidence map›Paper›PMID 38097595›Full record

ArticleNPJ Regenerative medicine2023

Effective protection of photoreceptors using an inflammation-responsive hydrogel to attenuate outer retinal degeneration.

Hyerim Kim, Hyeonhee Roh, Sang-Heon Kim, Kangwon Lee, Maesoon Im, Seung Ja Oh

Open access · goldAbstract read
In one paragraph

Article in NPJ Regenerative medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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    Article
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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

6 authors at 4 institutions in 2 countries.

Hyerim Kim *Program in Nanoscience and Technology, Graduate School of Convergence Science and Technology, Seoul National University, Seoul, 08826, South Korea.
Hyeonhee Roh *Brain Science Institute, Korea Institute of Science and Technology (KIST), Seoul, 02792, South Korea.
Sang-Heon KimCenter for Biomaterials, Biomedical Research Institute, KIST, Seoul, 02792, South Korea.ORCID http://orcid.org/0000-0002-6128-8218
Kangwon LeeDepartment of Applied Bioengineering, Graduate School of Convergence Science and Technology, Seoul National University, Seoul, 08826, South Korea. kangwonlee@snu.ac.kr.
Maesoon ImBrain Science Institute, Korea Institute of Science and Technology (KIST), Seoul, 02792, South Korea. maesoon.im@kist.re.kr.ORCID http://orcid.org/0000-0003-1152-4398
Seung Ja OhDepartment of Genetics and Biotechnology, College of Life Sciences, Kyung Hee University, Yongin, 17104, South Korea. seungja.oh@khu.ac.kr.
Kyung Hee University · KRSeoul National University of Science and Technology · KRBio-Medical Science (South Korea) · KRKorea University · KR

Funding

Korea Health Industry Development Institute (KHIDI) HI22C1394Korea Institute of Science and Technology (KIST) 2E32551National Research Foundation of Korea (NRF) 2017-Global Ph.D. Fellowship ProgramNational Research Foundation of Korea (NRF) 2021M3F3A2A01037366National Research Foundation of Korea (NRF) RS-2023-00208795
6 · The paper itself

Abstract

Retinitis pigmentosa (RP) is an outer retinal degenerative disease that can lead to photoreceptor cell death and profound vision loss. Although effective regulation of intraretinal inflammation can slow down the progression of the disease, an efficient anti-inflammatory treatment strategy is still lacking. This study reports the fabrication of a hyaluronic acid-based inflammation-responsive hydrogel (IRH) and its epigenetic regulation effects on retinal degeneration. The injectable IRH was designed to respond to cathepsin overexpression in an inflammatory environment. The epigenetic drug, the enhancer of zeste homolog 2 (EZH2) inhibitors, was loaded into the hydrogel to attenuate inflammatory factors. On-demand anti-inflammatory effects of microglia cells via the drug-loaded IRH were verified in vitro and in vivo retinal degeneration 10 (rd10) mice model. Therefore, our IRH not only reduced intraretinal inflammation but also protected photoreceptors morphologically and functionally. Our results suggest the IRH reported here can be used to considerably delay vision loss caused by RP.

Identifiers

PMID38097595
PMCPMC10721838
OpenAlexW4389764369

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.