Evidence map›Paper›PMID 36088291›Full record

ReviewCellular & molecular biology letters2022

Diversification of PAR signaling through receptor crosstalk.

Irene Lee-Rivera, Edith López, Ana María López-Colomé

Open access · goldAbstract readLetterReview
In one paragraph

Review in Cellular & molecular biology letters, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

  1. MMP1 and PRSS23 induce PARCommunications biology · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Serum from COVID-19 patients promotes endothelial cell dysfunction through protease-activated receptor 2.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
    Article
  12. 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

3 authors at 1 institution in 1 country.

Irene Lee-RiveraDepartment of Molecular Neuropathology, Instituto de Fisiología Celular, UNAM, Apartado Postal 70-253, Ciudad Universitaria, Mexico City, CdMx, Mexico.
Edith LópezDepartment of Molecular Neuropathology, Instituto de Fisiología Celular, UNAM, Apartado Postal 70-253, Ciudad Universitaria, Mexico City, CdMx, Mexico.
Ana María López-ColoméDepartment of Molecular Neuropathology, Instituto de Fisiología Celular, UNAM, Apartado Postal 70-253, Ciudad Universitaria, Mexico City, CdMx, Mexico. acolome@ifc.unam.mx.ORCID http://orcid.org/0000-0002-9574-1367
Instituto Nacional de Cardiología · MX

Funding

Programa de Apoyo a Proyectos de Investigación e Innovación Tecnológica (PAPIIT)/ Universidad Nacional Autónoma de México (UNAM) IN200220
6 · The paper itself

Abstract

Protease activated receptors (PARs) are among the first receptors shown to transactivate other receptors: noticeably, these interactions are not limited to members of the same family, but involve receptors as diverse as receptor kinases, prostanoid receptors, purinergic receptors and ionic channels among others. In this review, we will focus on the evidence for PAR interactions with members of their own family, as well as with other types of receptors. We will discuss recent evidence as well as what we consider as emerging areas to explore; from the signalling pathways triggered, to the physiological and pathological relevance of these interactions, since this additional level of molecular cross-talk between receptors and signaling pathways is only beginning to be explored and represents a novel mechanism providing diversity to receptor function and play important roles in physiology and disease.

Indexed as

Receptors, Proteinase-ActivatedSignal TransductionReceptors, Proteinase-ActivatedGPCR transactivationReceptor cofactoringReceptor dimerizationReceptor signalling crosstalk

Identifiers

PMID36088291
PMCPMC9463773
OpenAlexW4295512908

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.