Evidence map›Paper›PMID 29258882›Full record

ArticleOsteoarthritis and cartilage2018

Transcriptome comparison of meniscus from patients with and without osteoarthritis.

R H Brophy, B Zhang, L Cai, R W Wright, L J Sandell, M F Rai

Open access · greenAbstract read
In one paragraph

Article in Osteoarthritis and cartilage, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

54 citing papers in PubMed, 91 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. 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

6 authors at 1 institution in 1 country.

R H BrophyDepartment of Orthopaedic Surgery, Musculoskeletal Research Center, Washington University School of Medicine at Barnes-Jewish Hospital, 660 South Euclid Avenue, St. Louis, MO 63110, USA. Electronic address: brophyrh@wustl.edu.
B ZhangDepartment of Developmental Biology, Center of Regenerative Medicine, Washington University School of Medicine at Barnes-Jewish Hospital, 660 South Euclid Avenue, St. Louis, MO 63110, USA. Electronic address: bzhang29@wustl.edu.
L CaiDepartment of Orthopaedic Surgery, Musculoskeletal Research Center, Washington University School of Medicine at Barnes-Jewish Hospital, 660 South Euclid Avenue, St. Louis, MO 63110, USA. Electronic address: lei.cai@wustl.edu.
R W WrightDepartment of Orthopaedic Surgery, Musculoskeletal Research Center, Washington University School of Medicine at Barnes-Jewish Hospital, 660 South Euclid Avenue, St. Louis, MO 63110, USA. Electronic address: rwright@wustl.edu.
L J SandellDepartment of Orthopaedic Surgery, Musculoskeletal Research Center, Washington University School of Medicine at Barnes-Jewish Hospital, 660 South Euclid Avenue, St. Louis, MO 63110, USA; Department of Cell Biology and Physiology, Washington University School of Medicine at Barnes-Jewish Hospital, 660 South Euclid Avenue, St. Louis, MO 63110, USA; Department of Biomedical Engineering, Washington University School of Engineering & Applied Science, 1 Brookings Drive, St. Louis, MO 63130, USA. Electronic address: sandelll@wustl.edu.
M F RaiDepartment of Orthopaedic Surgery, Musculoskeletal Research Center, Washington University School of Medicine at Barnes-Jewish Hospital, 660 South Euclid Avenue, St. Louis, MO 63110, USA; Department of Cell Biology and Physiology, Washington University School of Medicine at Barnes-Jewish Hospital, 660 South Euclid Avenue, St. Louis, MO 63110, USA. Electronic address: rai.m@wustl.edu.
Barnes-Jewish Hospital · US

Funding

The Role of the Osteoblast Secretome in Bone FormationP30AR057235 · NIAMS · WASHINGTON UNIVERSITY · PI JOHNSON, AARON N · 2009 to 2018
$5.7M
RESEARCH EDUCATION PROGRAM ON COMPUTATIONAL AND STATISTICAL TOOL DEVELOPMENT FOR ADDICTION GENETICSR25DA027995 · NIDA · WASHINGTON UNIVERSITY · PI MADDEN, PAMELA ANN, RICE, JOHN P. · 2009 to 2019
$4.3M
Genetic and Molecular Insights into Cartilage Regeneration, Primary and Posttraumatic OsteoarthritisR00AR064837 · NIAMS · WASHINGTON UNIVERSITY · PI RAI, MUHAMMAD FAROOQ · 2017 to 2019
$747k
Genetics of Cartilage Regeneration and OsteoarthritisR01AR063757 · NIAMS · WASHINGTON UNIVERSITY · PI CHEVERUD, JAMES M, SANDELL, LINDA J · 2013 to 2014
$708k
Genetic and Molecular Insights Into Cartilage Regeneration, Primary and PosttraumK99AR064837 · NIAMS · WASHINGTON UNIVERSITY · PI RAI, MUHAMMAD FAROOQ · 2014 to 2015
$175k
NIAMS NIH HHS K99 AR064837NIAMS NIH HHS P30 AR057235NIAMS NIH HHS R00 AR064837NIAMS NIH HHS R01 AR063757NIDA NIH HHS R25 DA027995
6 · The paper itself

Abstract

objectiveTo assess the impact of osteoarthritis (OA) on the meniscus by comparing transcripts and biological processes in the meniscus between patients with and without OA.

designRNA microarrays were used to identify transcripts differentially expressed (DE) in meniscus obtained from 12 OA and 12 non-OA patients. The non-OA specimens were obtained at the time of arthroscopic partial meniscectomy. Real-time PCR was performed on selected transcripts. Biological processes and gene-networking was examined computationally. Transcriptome signatures were mapped with 37 OA-related transcripts to evaluate how meniscus gene expression relates to that of OA cartilage.

resultsWe identified 168 transcripts significantly DE between OA (75 elevated, 93 repressed) and non-OA samples (≥1.5-fold). Among these, CSN1S1, COL10A1, WIF1, and SPARCL1 were the most prominent transcripts elevated in OA meniscus, POSTN and VEGFA were most highly repressed in OA meniscus. Transcripts elevated in OA meniscus represented response to external stimuli, cell migration and cell localization while those repressed in OA meniscus represented histone deacetylase activity (related to epigenetics) and skeletal development. Numerous long non-coding RNAs (lncRNAs) were DE between the two groups. When segregated by OA-related transcripts, two distinct clustering patterns appeared: OA meniscus appeared to be more inflammatory while non-OA meniscus exhibited a "repair" phenotype.

conclusionsNumerous transcripts with potential relevance to the pathogenesis of OA are DE in OA and non-OA meniscus. These data suggest an involvement of epigenetically regulated histone deacetylation in meniscus tears as well as expression of lncRNAs. Patient clustering based on transcripts related to OA in articular cartilage confirmed distinct phenotypes between injured (non-OA) and OA meniscus.

Indexed as

Gene Expression ProfilingAgedCase-Control StudiesEpigenesis, GeneticFemaleGene ExpressionHumansMaleMeniscusMiddle AgedOligonucleotide Array Sequence AnalysisOsteoarthritisReal-Time Polymerase Chain ReactionTranscriptomeEpigeneticslncRNAsMeniscus tearMicroarraysOsteoarthritisPartial meniscectomy

Identifiers

PMID29258882
PMCPMC6007850
OpenAlexW2774945963

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.