Evidence mapPaperPMID 28736498Full record

ReviewBiochemia medica2017

Insights on glicentin, a promising peptide of the proglucagon family.

Juliette Raffort, Fabien Lareyre, Damien Massalou, Patrick Fénichel, Patricia Panaïa-Ferrari, Giulia Chinetti

Open access · diamondAbstract readReview
In one paragraph

Review in Biochemia medica, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 46 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Article
  5. Review
  6. Review
  7. Tanshinone-I for the treatment of uterine fibroids: Molecular docking, simulation, and density functional theory investigations.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2023
    Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Editorial: Proglucagon-Derived Peptides.Frontiers in endocrinology · 2021
    Article
  13. Article
  14. Review
  15. Proglucagon-Derived Peptides as Therapeutics.Frontiers in endocrinology · 2021
    Review
  16. Observational
  17. Review
  18. Observational
  19. Article
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

6 authors at 1 institution in 1 country.

Juliette RaffortClinical Chemistry Laboratory, University Hospital of Nice, Nice, France.
Fabien LareyreUniversité Côte d'Azur, Institute for Research on Cancer and Aging, Nice, France.
Damien MassalouDepartment of General Surgery and Digestive Cancerology, University Hospital of Nice, Nice, France.
Patrick FénichelDepartment of Endocrinology, University Hospital of Nice, Nice, France.
Patricia Panaïa-FerrariClinical Chemistry Laboratory, University Hospital of Nice, Nice, France.
Giulia ChinettiClinical Chemistry Laboratory, University Hospital of Nice, Nice, France.
Centre Hospitalier Universitaire de Nice · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glicentin is a proglucagon-derived peptide mainly produced in the L-intestinal cells. While the roles of other members of the proglucagon family including glucagon-like peptide 1, glucagon-like peptide 2 and oxyntomodulin has been well studied, the functions and variation of glicentin in human are not fully understood. Experimental and clinical studies have highlighted its role in both intestinal physiology and glucose metabolism, pointing to its potential interest in a wide range of pathological states including gastrointestinal and metabolic disorders. Due to its structure presenting many similarities with the other proglucagon-derived peptides, its measurement is technically challenging. The recent commercialization of specific detection methods has offered new opportunities to go further in the understanding of glicentin physiology. Here we summarize the current knowledge on glicentin biogenesis and physiological roles. In the limelight of clinical studies investigating glicentin variation in human, we discuss future directions for potential applications in clinical practice.

Indexed as

AnimalsGastric AcidGastrointestinal MotilityGene ExpressionGlicentinGlucoseHumansIntestinal MucosaIntestinesProglucagonGlicentinGlucoseProglucagonenteroendocrine cellsglicentinglucagon-like peptideoxyntomodulinproglucagon

Identifiers

PMID28736498
PMCPMC5508206
OpenAlexW2625013963

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.