Evidence map›Paper›PMID 29164451›Full record

ReviewPurinergic signalling2018

The potential of P2X7 receptors as a therapeutic target, including inflammation and tumour progression.

Geoffrey Burnstock, Gillian E Knight

Open access · hybridAbstract readReview
In one paragraph

Review in Purinergic signalling, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 154 papers.

0numbers the graph read from it
0cells of the map it votes in
154citing papers in PubMed
17.8field-weighted citation impact, top 1% 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

154 citing papers in PubMed, 241 citations in OpenAlex.

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94 more citing papers are in PubMed but not listed here.

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

2 authors at 2 institutions in 2 countries.

Geoffrey BurnstockAutonomic Neuroscience Centre, University College Medical School, Rowland Hill Street, London, NW3 2PF, UK. g.burnstock@ucl.ac.uk.ORCID http://orcid.org/0000-0001-8152-7979
Gillian E KnightAutonomic Neuroscience Centre, University College Medical School, Rowland Hill Street, London, NW3 2PF, UK.
Florey Institute of Neuroscience and Mental Health · AURoland Hill (United Kingdom) · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Seven P2X ion channel nucleotide receptor subtypes have been cloned and characterised. P2X7 receptors (P2X7R) are unusual in that there are extra amino acids in the intracellular C terminus. Low concentrations of ATP open cation channels sometimes leading to cell proliferation, whereas high concentrations of ATP open large pores that release inflammatory cytokines and can lead to apoptotic cell death. Since many diseases involve inflammation and immune responses, and the P2X7R regulates inflammation, there has been recent interest in the pathophysiological roles of P2X7R and the potential of P2X7R antagonists to treat a variety of diseases. These include neurodegenerative diseases, psychiatric disorders, epilepsy and a number of diseases of peripheral organs, including the cardiovascular, airways, kidney, liver, bladder, skin and musculoskeletal. The potential of P2X7R drugs to treat tumour progression is discussed.

Indexed as

AnimalsDisease ProgressionHumansInflammationNeoplasmsPurinergic P2X Receptor AntagonistsReceptors, Purinergic P2X7Purinergic P2X Receptor AntagonistsReceptors, Purinergic P2X7AirwaysBladderCancerCardiovascularCNS disordersDiabetesGutImmune cellsInfectionKidneyLiverPain

Identifiers

PMID29164451
PMCPMC5842154
OpenAlexW2768734810

What Socratic 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 Socratic graph.