Evidence map›Paper›PMID 28898282›Full record

ArticlePloS one2017

P2X3 receptor involvement in endometriosis pain via ERK signaling pathway.

Shaojie Ding, Libo Zhu, Yonghong Tian, Tianhong Zhu, Xiufeng Huang, Xinmei Zhang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
6.1field-weighted citation impact, top 4% 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

26 citing papers in PubMed, 53 citations in OpenAlex.

  1. Trial
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  11. Chronic cough: new insights and future prospects.European respiratory review : an official journal of the European Respiratory Society · 2021
    Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. P2XThe journal of headache and pain · 2021
    Article
  17. Article
  18. Article
  19. Article
  20. Purinergic Signaling in Endometriosis-Associated Pain.International journal of molecular sciences · 2020
    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.

Shaojie DingWomen's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, P.R. China.
Libo ZhuWomen's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, P.R. China.
Yonghong TianWomen's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, P.R. China.
Tianhong ZhuWomen's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, P.R. China.
Xiufeng HuangWomen's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, P.R. China.
Xinmei ZhangWomen's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, P.R. China.ORCID http://orcid.org/0000-0001-7122-6435
Women's Hospital, School of Medicine, Zhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The purinergic receptor P2X ligand-gated ion channel 3 (P2X3) is crucially involved in peripheral nociceptive processes of somatic and visceral pain. Endometriosis pain is considered as a kind of inflammatory and neuropathic pain. However, whether P2X3 is involved in endometriosis pain has not been reported up to date. Here, we aimed to determine whether P2X3 expression in endometriotic lesions is involved in endometriosis pain, which is regulated by inflammatory mediators through extracellular regulated protein kinases (ERK) signalling pathway. We found that P2X3 expressions in endometriosis endometrium and endometriotic lesions were both significantly higher as compared with control endometrium (P<0.05), and both positively correlated with pain (P<0.05). The expression levels of phosphorylated -ERK (p-ERK), phosphorylated-cAMP-response element binding protein (p-CREB), and P2X3 in endometriotic stromal cells (ESCs) were all significantly increased in comparison to the initial levels after treated with interleukin (IL)-1β (P<0.05) or adenosine triphosphate (ATP) (P<0.05), respectively, and did not increase after the ESCs were pre-treated with ERK1/2 inhibitor. Additionally, P2X3 and calcitonin gene related peptide (CGRP) were co-expressed in endometriotic lesions. These obtained results suggest that P2X3 might be involved in endometriosis pain signal transduction via ERK signal pathway.

Indexed as

AdultCalcitonin Gene-Related PeptideCase-Control StudiesCyclic AMP Response Element-Binding ProteinEndometriosisFemaleHumansMAP Kinase Signaling SystemMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Receptors, Purinergic P2X3Stromal CellsVisceral PainCalcitonin Gene-Related PeptideCyclic AMP Response Element-Binding ProteinMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Receptors, Purinergic P2X3

Identifiers

PMID28898282
PMCPMC5595329
OpenAlexW2754165634

What OpenQuestion holds

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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.