Evidence map›Paper›PMID 18698181›Full record

ReviewCurrent opinion in rheumatology2008

Mitogen-activated protein kinases as therapeutic targets in osteoarthritis.

Richard F Loeser, Elizabeth A Erickson, David L Long

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in rheumatology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

78 citing papers in PubMed, 149 citations in OpenAlex.

  1. CSPG4Osteoarthritis and cartilage open · 2026
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  18. WGA-M001, a Mixture of Total Extracts ofInternational journal of molecular sciences · 2023
    Article
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18 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

3 authors at 1 institution in 1 country.

Richard F LoeserDepartment of Internal Medicine, Section of Molecular Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina 27157, USA. rloeser@wfubmc.edu
Elizabeth A Erickson
David L Long
Wake Forest University · US

Funding

Integrin Function in CartilageR37AR049003 · NIAMS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LOESER, RICHARD F · 2012 to 2021
$4.1M
Integrin Function in CartilageR01AR049003 · NIAMS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LOESER, RICHARD F · 2002 to 2011
$2.8M
Aging and IGF-I in CartilageR01AG016697 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LOESER, RICHARD F · 2001 to 2009
$2.4M
Training Program in Molecular MedicineT32GM063485 · NIGMS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI BROSNIHAN, KATHLEEN BRIDGET · 2004 to 2008
$757k
Elucidating the JNK2-mediated redox regulation of cartilage matrix remdelingF31AG032796 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ERICKSON, ELIZABETH ALICE · 2008 to 2010
$124k
NIAMS NIH HHS AR49003NIAMS NIH HHS R01 AR049003NIAMS NIH HHS R37 AR049003NIA NIH HHS AG16697NIA NIH HHS F31 AG032796NIA NIH HHS R01 AG016697NIGMS NIH HHS GM063485NIGMS NIH HHS T32 GM063485
6 · The paper itself

Abstract

purpose of reviewThe mitogen-activated protein (MAP) kinases are intracellular signaling proteins which play a central role in controlling the activity of pathways that regulate production and activity of multiple mediators of joint tissue destruction. The therapeutic potential of MAP kinase inhibition in osteoarthritis was reviewed. RECENT

findingsResults from basic research studies support the role of MAP kinases as central mediators that regulate expression of proinflammatory cytokines and metalloproteinases but also as potential pain mediators as well. Cell culture and animal model studies suggest that inhibition of MAP kinases might slow progression of osteoarthritis but trials of MAP kinase inhibitors in humans with osteoarthritis have not yet been reported. Safety concerns of the currently available inhibitors have limited their initial use to trials in conditions considered more severe than osteoarthritis. SUMMARY: MAP kinase inhibition has the potential to slow disease progression in osteoarthritis and also might reduce pain; however, safety concerns have limited the use of general MAP kinase inhibitors in humans. Further understanding of the function of specific isoforms of the MAP kinases as well as upstream and downstream effectors may lead to the development of more specific inhibitors with less toxicity that could eventually be used as structure-modifying drugs for osteoarthritis.

Indexed as

AnimalsCartilage, ArticularEnzyme InhibitorsHumansMAP Kinase Signaling SystemMitogen-Activated Protein KinasesOsteoarthritisEnzyme InhibitorsMitogen-Activated Protein Kinases

Identifiers

PMID18698181
PMCPMC2892710
OpenAlexW2094115539

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.