Evidence map›Paper›PMID 32838583›Full record

ReviewExpert opinion on therapeutic targets2020

TRPA1 as a therapeutic target for nociceptive pain.

Daniel Souza Monteiro de Araujo, Romina Nassini, Pierangelo Geppetti, Francesco De Logu

Open access · bronzeAbstract readReview
In one paragraph

Review in Expert opinion on therapeutic targets, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 117 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
117citing papers in PubMed, 1 pooled it
7.2field-weighted citation impact, top 2% 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

117 citing papers in PubMed, 1 synthesis or guideline pooled it, 211 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Skin pain in pediatric atopic dermatitis: mechanisms and management.Current opinion in allergy and clinical immunology · 2026
    Review
  8. Review
  9. Review
  10. Europium Metal Complex [Eu(dbm)Chemistry & biodiversity · 2026
    Article
  11. Article
  12. Article
  13. The paraEuropean journal of pain (London, England) · 2026
    Article
  14. Review
  15. Review
  16. Molecular divergence ofZoological research · 2026
    Article
  17. Review
  18. Article
  19. Review
  20. Article

57 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

4 authors at 1 institution in 1 country.

Daniel Souza Monteiro de AraujoDepartment of Health Sciences, Clinical Pharmacology Unit, University of Florence , Florence, Italy.
Romina NassiniDepartment of Health Sciences, Clinical Pharmacology Unit, University of Florence , Florence, Italy.
Pierangelo GeppettiDepartment of Health Sciences, Clinical Pharmacology Unit, University of Florence , Florence, Italy.
Francesco De LoguDepartment of Health Sciences, Clinical Pharmacology Unit, University of Florence , Florence, Italy.
University of Florence · IT

Funding

European Research Council 835286
6 · The paper itself

Abstract

introductionChronic pain affects approximatively 30-50% of the population globally. Pathologies such as migraine, diabetic neuropathy, nerve injury and treatment with chemotherapeutic agents, can induce chronic pain. Members of the transient receptor potential (TRP) channels, including the TRP ankyrin 1 (TRPA1), have a major role in pain. AREAS COVERED: We focus on TRPA1 as a therapeutic target for pain relief. The structure, localization, and activation of the channel and its implication in different pathways to signal pain are described. This paper underlines the role of pharmacological interventions on TRPA1 to reduce pain in numerous pain conditions. We conducted a literature search in PubMed up to and including July 2020. EXPERT OPINION: Our understanding of the molecular mechanisms underlying the sensitization of central and peripheral nociceptive pathways is limited. Preclinical evidence indicates that, in murine models of pain diseases, numerous mechanisms converge on the pathway that encompasses oxidative stress and Schwann cell TRPA1 to sustain chronic pain. Programs to identify and develop treatments to attenuate TRPA1-mediated chronic pain have emerged from this knowledge. Antagonists explored as a novel class of analgesics have a new and promising target in the TRPA1 expressed by peripheral glial cells.

Indexed as

Molecular Targeted TherapyAnalgesicsAnimalsChronic PainDisease Models, AnimalHumansMiceNociceptive PainOxidative StressTRPA1 Cation ChannelAnalgesicsTRPA1 Cation ChannelTRPA1 protein, humanInflammatory painneuropathic painnociceptionTransient Receptor Potential (TRP) channelsTRP ankyrin 1 (TRPA1)

Identifiers

PMID32838583
PMCPMC7610834
OpenAlexW3080513507

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.