Evidence map›Paper›PMID 23926636›Full record

ReviewCurrent rheumatology reports2013

Genetically Engineered Mouse Models Reveal the Importance of Proteases as Osteoarthritis Drug Targets.

Rachel E Miller, Yongzhi Lu, Micky D Tortorella, Anne-Marie Malfait

Open access · greenAbstract readReview
In one paragraph

Review in Current rheumatology reports, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Review
  3. Animal Models of Osteoarthritis: Updated Models and Outcome Measures 2016-2023.Regenerative engineering and translational medicine · 2024
    Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Basic science of osteoarthritis.Journal of experimental orthopaedics · 2016
    Article
  12. Review
  13. Article
  14. Article
  15. Emerging targets in osteoarthritis therapy.Current opinion in pharmacology · 2015
    Review
  16. Article
  17. 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

4 authors at 3 institutions in 2 countries.

Rachel E MillerDepartment of Medicine, Section of Rheumatology, Rush University Medical Center, 1611 W. Harrison St., Suite 510, Chicago, IL 60612, USA.
Yongzhi Lu
Micky D Tortorella
Anne-Marie Malfait
Rush University Medical Center · USChinese Academy of Sciences · CNGuangzhou Institutes of Biomedicine and Health · CN

Funding

Molecular Pathways of Pain Generation in OsteoarthritisR01AR060364 · NIAMS · RUSH UNIVERSITY MEDICAL CENTER · PI MALFAIT, ANNE-MARIE · 2011 to 2025
$6.0M
MCP-1/CCR2 Signaling in the Maintenance of OA Pathology and Associated PainF32AR062927 · NIAMS · RUSH UNIVERSITY MEDICAL CENTER · PI MILLER, RACHEL ELIZABETH · 2013 to 2015
$131k
NIAMS NIH HHS F32 AR062927NIAMS NIH HHS R01 AR060364NIAMS NIH HHS R01AR060364
6 · The paper itself

Abstract

More than two decades of research has revealed a combination of proteases that determine cartilage degradation in osteoarthritis. These include metalloproteinases, which degrade the major macromolecules in cartilage, aggrecan and type II collagen, serine proteases, and cysteine proteases, for example cathepsin K. This review summarizes the function of proteases in osteoarthritis progression, as revealed by studies of genetically engineered mouse models. A brief overview of the biochemical characteristics and features of several important proteases is provided, with the objective of increasing understanding of their function. Published data reveal at least three enzymes to be major targets for osteoarthritis drug development: ADAMTS-5, MMP-13, and cathepsin K. In surgical models of osteoarthritis, mice lacking these enzymes are protected from cartilage damage and, to varying degrees, from bone changes. In-vivo studies targeting these proteases with selective small-molecule inhibitors have been performed for a variety of animal models. Mouse models will provide opportunities for future tests of the therapeutic effect of protease inhibitors, both on progression of structural damage to the joint and on associated pain.

Indexed as

AnimalsAnimals, Genetically ModifiedArthritis, ExperimentalCatalysisDrug DesignHumansMiceOsteoarthritisPeptide HydrolasesProtease InhibitorsStructure-Activity RelationshipPeptide HydrolasesProtease Inhibitors

Identifiers

PMID23926636
PMCPMC4062186
OpenAlexW2094963928

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.