Evidence map›Paper›PMID 39483974›Full record

ArticleJournal of tissue engineering

Targeting ROS in osteoclasts within the OA environment: A novel therapeutic strategy for osteoarthritis management.

Seungho Jeon, Tae Min Kim, Gitae Kwon, Junyoung Park, Sung Young Park, Seoung Hoon Lee, Eun-Jung Jin

Abstract read
In one paragraph

Article in Journal of tissue engineering. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. ROS-Sensitive MgOSiOInternational journal of nanomedicine · 2025
    Article
  8. 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

7 authors.

Seungho JeonDepartment of Biological Sciences, Wonkwang, University, Iksan, Jeonbuk, South Korea.
Tae Min KimDepartment of IT and Energy Convergence (BK21 FOUR), Korea National University of Transportation, Chungju, South Korea.
Gitae KwonDepartment of Biological Sciences, Wonkwang, University, Iksan, Jeonbuk, South Korea.
Junyoung ParkDepartment of Biological Sciences, Wonkwang, University, Iksan, Jeonbuk, South Korea.
Sung Young ParkDepartment of IT and Energy Convergence (BK21 FOUR), Korea National University of Transportation, Chungju, South Korea.
Seoung Hoon LeeDepartment of Oral Microbiology and Immunology, College of Dentistry, Wonkwang University, Iksan, Jeonbuk, Korea.
Eun-Jung JinDepartment of Biological Sciences, Wonkwang, University, Iksan, Jeonbuk, South Korea.ORCID https://orcid.org/0000-0002-6874-3017

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study investigated the therapeutic potential of a manganese dioxide-polymer dot (MnO2-PD)-incorporated hydrogel, designated as M-PD hydrogel, for modulating reactive oxygen species (ROS) within the osteoarthritis (OA) environment. Our research highlights the ability of the hydrogel to scavenge ROS, thereby influencing the differentiation of osteoclasts and protecting chondrocytes, offering a novel approach to osteoarthritis (OA) management. Our results indicated that the M-PD hydrogel increased electrical resistance and fluorescence recovery in the presence of osteoclasts, correlating with decreased ROS levels and suppressed expression of osteoclast differentiation markers. Coculture experiments revealed the protective effects of the hydrogel on chondrocytes by reducing the expression of matrix-degrading enzymes. In vivo application in burr holes and/or OA-induced mice revealed a significant reduction in osteoclast formation and cartilage destruction, suggesting the dual therapeutic action of the hydrogel in altering the joint microenvironment. These findings highlight the potential of targeting ROS in osteoclasts as a comprehensive therapeutic approach, offering not only symptomatic relief but also targeting the underlying mechanisms of disease progression in OA.

Indexed as

joint microenvironmentM-PD hydrogelosteoarthritisosteoclastROS

Identifiers

PMID39483974
PMCPMC11526208

What OpenQuestion holds

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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.