Evidence map›Paper›PMID 20839316›Full record

ArticleJournal of orthopaedic research : official publication of the Orthopaedic Research Society2010

Prostaglandin E2 and prostaglandin F2α differentially modulate matrix metabolism of human nucleus pulposus cells.

Nam V Vo, Gwendolyn A Sowa, James D Kang, Christopher Seidel, Rebecca K Studer

Open access · bronzeAbstract read
In one paragraph

Article in Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 2010. 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
0.7field-weighted citation impact, top 27% 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, 28 citations in OpenAlex.

  1. Article
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  3. Review
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  6. Review
  7. Article
  8. Article
  9. Oxidative medicine and cellular longevity · 2018
    Article
  10. NSAID use in intervertebral disc degeneration: what are the effects on matrix homeostasis in vivo?The spine journal : official journal of the North American Spine Society · 2017
    Article
  11. Article
  12. Article
  13. Article
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  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

5 authors at 4 institutions in 1 country.

Nam V VoFerguson Laboratory for Orthopaedic Research, University of Pittsburgh Medical School, Pittsburgh, Pennsylvania, USA. von@upmc.edu
Gwendolyn A Sowa
James D Kang
Christopher Seidel
Rebecca K Studer
University of Pittsburgh · USStowers Institute for Medical Research · USUniversity of Pittsburgh Medical Center · USVA Pittsburgh Healthcare System · US

Funding

VARIABILITY, STABILITY & SMOOTHNESS OF WALKINGP30AG024827 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JENNIFER S BRACH · 2004 to 2026
$28.6M
MECHANISM OF DISC PROTEOGLYCAN LOSS IN A MOUSE MODEL OF ACCELERATED AGINGR21AG033046 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI VO, NAM V · 2010 to 2011
$328k
NIA NIH HHS P30 AG024827NIA NIH HHS R21 AG033046
6 · The paper itself

Abstract

Prostaglandin (PG) actions on disc metabolism are unclear even though certain PGs are highly expressed by disc cells under inflammatory conditions and nonsteroidal anti-inflammatory drugs (NSAIDs) are frequently used to block PG production to treat back pain. Hence this study aimed to (1) quantify gene expression of arachidonic acid cascade components responsible for PG synthesis and (2) examine the effects of key PGs on disc matrix homeostasis. Microarray analysis revealed that inflammatory stress increases expression of synthases and receptors for prostaglandin E2 (PGE(2)) and prostaglandin F2α (PGF(2α)), resulting in elevated PGE(2) and PGF(2α) production in conditioned media of disc cells. PGE(2) diminished disc cell proteoglycan synthesis, in a dose-dependent manner. Semiquantitative RT-PCR revealed differential effects of PGE(2) and PGF(2α) on disc cell expression of key matrix structural genes, aggrecan, versican, collagens type I and II. PGE(2) and PGF(2α) also decreased message for the anabolic factor, IGF-1. PGE(2) decreased mRNA expression for the anti-catabolic factor TIMP-1 while PGF(2α) increased mRNAs for catabolic factors MMP-1 and MMP-3. Thus, PGE(2) and PGF(2α) may have an overall negative impact on disc matrix homeostasis, and the use of NSAIDs may impact disc metabolism as well as treat back pain.

Indexed as

AdultAggrecansAnti-Inflammatory Agents, Non-SteroidalArachidonic AcidCells, CulturedCollagen Type ICollagen Type IIDinoprostDinoprostoneHumansIntervertebral DiscMatrix Metalloproteinase 1Matrix Metalloproteinase 3Middle AgedTissue Inhibitor of Metalloproteinase-1VersicansAggrecansAnti-Inflammatory Agents, Non-SteroidalArachidonic AcidCollagen Type ICollagen Type IIDinoprostDinoprostoneMatrix Metalloproteinase 1Matrix Metalloproteinase 3Tissue Inhibitor of Metalloproteinase-1Versicans

Identifiers

PMID20839316
PMCPMC4810446
OpenAlexW2076388773

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.