Evidence map›Paper›PMID 36878303›Full record

ReviewBiochimica et biophysica acta. Molecular basis of disease2023

The clinical relevance of the adhesion G protein-coupled receptor F5 for human diseases and cancers.

Damian Jacenik, Pawel Hikisz, Ellen J Beswick, Jakub Fichna

Open access · hybridAbstract readReview
In one paragraph

Review in Biochimica et biophysica acta. Molecular basis of disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.8field-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

8 citing papers in PubMed, 12 citations in OpenAlex.

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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 3 institutions in 2 countries.

Damian JacenikDepartment of Cytobiochemistry, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland. Electronic address: damian.jacenik@biol.uni.lodz.pl.
Pawel HikiszDepartment of Oncobiology and Epigenetics, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland. Electronic address: pawel.hikisz@biol.uni.lodz.pl.
Ellen J BeswickDivision of Gastroenterology, Department of Internal Medicine, University of Kentucky, Lexington, KY, United States. Electronic address: ebeswick@gmail.com.
Jakub FichnaDepartment of Biochemistry, Faculty of Medicine, Medical University of Lodz, Lodz, Poland. Electronic address: jakub.fichna@umed.lodz.pl.
University of Łódź · PLMedical University of Lodz · PLUniversity of Kentucky · US

Funding

G-CSF inhibition as a colorectal cancer therapyR01CA207051 · NCI · UNIVERSITY OF UTAH · PI BESWICK, ELLEN J. · 2016 to 2021
$1.7M
NCI NIH HHS R01 CA207051
6 · The paper itself

Abstract

Among the numerous adhesion G protein-coupled receptors (GPCRs), adhesion G protein-coupled estrogen receptor F5 (ADGRF5) contains unique domains in the long N-terminal tail which can determine cell-cell and cell-matrix interaction as well as cell adhesion. Nevertheless, the biology of ADGRF5 is complex and still poorly explored. Accumulating evidence suggests that the ADGRF5 activity is fundamental in health and disease. For instance, ADGRF5 is essential in the proper function of lungs and kidney as well as the endocrine system, and its signification in vascularization and tumorigenesis has been demonstrated. The most recent studies have provided findings about the diagnostic potential of ADGRF5 in osteoporosis and cancers, and ongoing studies suggest other diseases as well. Here, we elaborate on the current state of knowledge about the ADGRF5 in the physiology and pathophysiology of human diseases and highlight its high potential as a novel target in various therapeutic areas.

Indexed as

Clinical RelevanceNeoplasmsCell AdhesionHumansLungReceptors, G-Protein-CoupledADGRF5 protein, humanReceptors, G-Protein-CoupledADGRF5Adhesion G protein-coupled receptorAdhesion G protein-coupled receptor F5GPR116G protein-coupled receptor 116Ig-Hepta

Identifiers

PMID36878303
PMCPMC10164118
OpenAlexW4323073136

What OpenQuestion holds

Textmetadata
LicenceTDM
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.