Evidence map›Paper›PMID 27306986›Full record

ReviewJournal of internal medicine2017

Targeting orphan G protein-coupled receptors for the treatment of diabetes and its complications: C-peptide and GPR146.

G R Kolar, S M Grote, G L C Yosten

Abstract readReview
In one paragraph

Review in Journal of internal medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

15 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Structural insights into regulation of CCN protein activities and functions.Journal of cell communication and signaling · 2023
    Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. A C-peptide complex with albumin and ZnScientific reports · 2020
    Article
  12. Review
  13. Review
  14. Article
  15. 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.

G R KolarDepartment of Pathology, St Louis University School of Medicine, St Louis, MO, USA.
S M GroteDepartment of Pharmacology and Physiology, St Louis University School of Medicine, St Louis, MO, USA.
G L C YostenDepartment of Pharmacology and Physiology, St Louis University School of Medicine, St Louis, MO, USA.
Saint Louis University · US

Funding

Angiotensin Receptor Regulation By Upstream Short Open Reading FramesR01HL121456 · NHLBI · GEORGETOWN UNIVERSITY · PI SAMSON, WILLIS K., SANDBERG, KATHRYN L · 2014 to 2017
$3.1M
NHLBI NIH HHS R01 HL121456
6 · The paper itself

Abstract

G protein-coupled receptors (GPCRs) are the most abundant receptor family encoded by the human genome and are the targets of a high percentage of drugs currently in use or in clinical trials for the treatment of diseases such as diabetes and its associated complications. Thus, orphan GPCRs, for which the ligand is unknown, represent an important untapped source of therapeutic potential for the treatment of many diseases. We have identified the previously orphan GPCR, GPR146, as the putative receptor of proinsulin C-peptide, which may prove to be an effective treatment for diabetes-associated complications. For example, we have found a potential role of C-peptide and GPR146 in regulating the function of the retinal pigment epithelium, a monolayer of cells in the retina that serves as part of the blood-retinal barrier and is disrupted in diabetic macular oedema. However, C-peptide signalling in this cell type appears to depend at least in part on extracellular glucose concentration and its interaction with insulin. In this review, we discuss the therapeutic potential of orphan GPCRs with a special focus on C-peptide and GPR146, including past and current strategies used to 'deorphanize' this diverse family of receptors, past successes and the inherent difficulties of this process.

Indexed as

AnimalsCell DifferentiationC-PeptideDiabetes ComplicationsDiabetes MellitusGlucoseHumansHypoglycemic AgentsInsulinReceptors, G-Protein-CoupledRetinal Pigment EpitheliumSignal TransductionC-PeptideGlucoseGPR146 protein, humanHypoglycemic AgentsInsulinReceptors, G-Protein-CoupledC-peptidediabetesdiabetes-associated complicationsGPR146G protein-coupled receptororphan GPCR

Identifiers

PMID27306986
PMCPMC6092955
OpenAlexW2427097125

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.