Evidence map›Paper›PMID 31333416›Full record

ArticleFrontiers in cellular neuroscience2019

Mast Cell/Proteinase Activated Receptor 2 (PAR2) Mediated Interactions in the Pathogenesis of Discogenic Back Pain.

Justin Richards, Shirley Tang, Gilian Gunsch, Pavel Sul, Matthew Wiet, David C Flanigan, Safdar N Khan, Sarah Moore, Benjamin Walter, Devina Purmessur

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Updates on Pathophysiology of Discogenic Back Pain.Journal of clinical medicine · 2023
    Review
  9. Article
  10. Article
  11. Frontiers in pain research (Lausanne, Switzerland) · 2022
    Review
  12. Article
  13. Review
  14. Article
  15. 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

10 authors at 3 institutions in 1 country.

Justin RichardsCollege of Arts and Sciences, The Ohio State University, Columbus, OH, United States.
Shirley TangCollege of Engineering, The Ohio State University, Columbus, OH, United States.
Gilian GunschCollege of Arts and Sciences, The Ohio State University, Columbus, OH, United States.
Pavel SulCollege of Engineering, The Ohio State University, Columbus, OH, United States.
Matthew WietCollege of Engineering, The Ohio State University, Columbus, OH, United States.
David C FlaniganDepartment of Orthopaedics, Wexner Medical Center, The Ohio State University, Columbus, OH, United States.
Safdar N KhanDepartment of Orthopaedics, Wexner Medical Center, The Ohio State University, Columbus, OH, United States.
Sarah MooreCollege of Veterinary Medicine, The Ohio State University, Columbus, OH, United States.
Benjamin WalterCollege of Engineering, The Ohio State University, Columbus, OH, United States.
Devina PurmessurCollege of Engineering, The Ohio State University, Columbus, OH, United States.
The Ohio State University · USThe Ohio State University Wexner Medical Center · USFlorida State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mast cells (MCs) are present in the painful degenerate human intervertebral disc (IVD) and are associated with disease pathogenesis. MCs release granules containing enzymatic and inflammatory factors in response to stimulants or allergens. The serine protease, tryptase, is unique to MCs and its activation of the G-protein coupled receptor, Protease Activated Receptor 2 (PAR2), induces inflammation and degradation in osteoarthritic cartilage. Our previously published work has demonstrated increased levels of MC marker tryptase in IVD samples from discogenic back pain patients compared to healthy control IVD samples including expression of chemotactic agents that may facilitate MC migration into the IVD. To further elucidate MCs' role in the IVD and mechanisms underlying its effects, we investigated whether (1) human IVD cells can promote MC migration, (2) MC tryptase can mediate up-regulation of inflammatory/catabolic process in human IVD cells and tissue, and (3) the potential of PAR2 antagonist to function as a therapeutic drug in

Indexed as

discogenic back painintervertebral discmast cellPAR2tryptase

Identifiers

PMID31333416
PMCPMC6625229
OpenAlexW2952454142

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.