Evidence map›Paper›PMID 33572320›Full record

ReviewInternational journal of molecular sciences2021

Overview of MMP-13 as a Promising Target for the Treatment of Osteoarthritis.

Qichan Hu, Melanie Ecker

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 279 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
279citing papers in PubMed, 1 pooled it
23.9field-weighted citation impact, top 1% 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

279 citing papers in PubMed, 1 synthesis or guideline pooled it, 440 citations in OpenAlex.

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  16. REJENERAInflammopharmacology · 2026
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219 more citing papers are in PubMed but not listed here.

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

2 authors at 1 institution in 1 country.

Qichan HuDepartment of Biomedical Engineering, University of North Texas, Denton, TX 76203, USA.
Melanie EckerDepartment of Biomedical Engineering, University of North Texas, Denton, TX 76203, USA.ORCID 0000-0002-0603-6683
University of North Texas · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoarthritis (OA) is a common degenerative disease characterized by the destruction of articular cartilage and chronic inflammation of surrounding tissues. Matrix metalloproteinase-13 (MMP-13) is the primary MMP involved in cartilage degradation through its particular ability to cleave type II collagen. Hence, it is an attractive target for the treatment of OA. However, the detailed molecular mechanisms of OA initiation and progression remain elusive, and, currently, there are no interventions available to restore degraded cartilage. This review fully illustrates the involvement of MMP-13 in the initiation and progression of OA through the regulation of MMP-13 activity at the molecular and epigenetic levels, as well as the strategies that have been employed against MMP-13. The aim of this review is to identify MMP-13 as an attractive target for inhibitor development in the treatment of OA.

Indexed as

Cartilage, ArticularCatalytic DomainCollagen Type IICrystallography, X-RayDisease ProgressionDrug DevelopmentEpigenesis, GeneticHumansHydrophobic and Hydrophilic InteractionsMatrix Metalloproteinase 13Matrix Metalloproteinase InhibitorsMolecular Targeted TherapyOsteoarthritisCollagen Type IIMatrix Metalloproteinase 13Matrix Metalloproteinase InhibitorsMMP13 protein, humancartilageinhibitormatrix metalloproteinasesMMP-13osteoarthritisregulationtype II collagen

Identifiers

PMID33572320
PMCPMC7916132
OpenAlexW3128044437

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.