Evidence map›Paper›PMID 30970348›Full record

ReviewGerontology2019

Epigenetic Mechanisms Underlying the Aging of Articular Cartilage and Osteoarthritis.

Mingcai Zhang, Justin L Theleman, Katherine A Lygrisse, Jinxi Wang

Open access · bronzeAbstract readReview
In one paragraph

Review in Gerontology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

34 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Cellular senescence in skeletal disease: mechanisms and treatment.Cellular & molecular biology letters · 2023
    Review
  15. Article
  16. Article
  17. Review
  18. Regulatory role of NFAT1 signaling in articular chondrocyte activities and osteoarthritis pathogenesis.Biocell : official journal of the Sociedades Latinoamericanas de Microscopia Electronica ... et. al · 2023
    Article
  19. Article
  20. Review
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 1 country.

Mingcai ZhangDepartment of Orthopedic Surgery, Harrington Laboratory for Molecular Orthopedics, Kansas City, Kansas, USA.
Justin L ThelemanDepartment of Orthopedic Surgery, Harrington Laboratory for Molecular Orthopedics, Kansas City, Kansas, USA.
Katherine A LygrisseDepartment of Orthopedic Surgery, Harrington Laboratory for Molecular Orthopedics, Kansas City, Kansas, USA.
Jinxi WangDepartment of Orthopedic Surgery, Harrington Laboratory for Molecular Orthopedics, Kansas City, Kansas, USA, jwang@kumc.edu.
Harrington Cancer Center · USThe University of Kansas Health System · USUniversity of Kansas Medical Center · US

Funding

Transcription Factor NFAT1 Deficiency and OsteoarthritisR01AR059088 · NIAMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI WANG, JINXI · 2011 to 2015
$1.7M
NIAMS NIH HHS R01 AR059088
6 · The paper itself

Abstract

Aging is a progressive and complicated bioprocess with overall decline in physiological function. Osteoarthritis (OA) is the most common joint disease in middle-aged and older populations. Since the prevalence of OA increases with age and breakdown of articular cartilage is its major hallmark, OA has long been thought of as "wear and tear" of joint cartilage. Nevertheless, recent studies have revealed that changes in the chondrocyte function and matrix components may reduce the material properties of articular cartilage and predispose the joint to OA. The aberrant gene expression in aging articular cartilage that is regulated by various epigenetic mechanisms plays an important role in age-related OA pathogenesis. This review begins with an introduction to the current understanding of epigenetic mechanisms, followed by mechanistic studies on the aging of joint tissues, epigenetic regulation of age-dependent gene expression in articular cartilage, and the significance of epigenetic mechanisms in OA pathogenesis. Our recent findings on age-dependent expression of 2 transcription factors, nuclear factor of activated T cell 1 (NFAT1) and SOX9, and their roles in the formation and aging of articular cartilage are summarized in the review. Chondrocyte dysfunction in aged mice, which is mediated by epigenetically regulated spontaneous reduction of NFAT1 expression in articular cartilage, is highlighted as an important advance in epigenetics and cartilage aging. Potential therapeutic strategies for age-related cartilage degeneration and OA using epigenetic molecular tools are discussed at the end.

Indexed as

Epigenesis, GeneticGene ExpressionAgingAnimalsBiomechanical PhenomenaCartilage, ArticularChondrocytesExtracellular MatrixHumansMiceNFATC Transcription FactorsOsteoarthritisSOX9 Transcription FactorNFATC Transcription FactorsSOX9 Transcription FactorAgingArticular cartilageEpigeneticsGene expressionNuclear factor of activated T cell 1Osteoarthritis

Identifiers

PMID30970348
PMCPMC9150844
OpenAlexW2935761054

What OpenQuestion holds

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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.