Evidence map›Paper›PMID 35966051›Full record

ReviewFrontiers in endocrinology2022

The Orexin receptors: Structural and anti-tumoral properties.

Alain Couvineau, Pascal Nicole, Valérie Gratio, Thierry Voisin

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Synthesis of Pyrrolo[3,4-Pharmaceuticals (Basel, Switzerland) · 2023
    Article
  12. Polypharmacology: promises and new drugs in 2022.Pharmacological reports : PR · 2023
    Review
  13. 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

4 authors at 3 institutions in 1 country.

Alain CouvineauINSERM UMR-S1149/Center of Research on Inflammation (CRI), Université Paris Cité, Team "From Inflammation to Cancer in Digestive Diseases", DHU UNITY, Paris, France.
Pascal NicoleINSERM UMR-S1149/Center of Research on Inflammation (CRI), Université Paris Cité, Team "From Inflammation to Cancer in Digestive Diseases", DHU UNITY, Paris, France.
Valérie GratioINSERM UMR-S1149/Center of Research on Inflammation (CRI), Université Paris Cité, Team "From Inflammation to Cancer in Digestive Diseases", DHU UNITY, Paris, France.
Thierry VoisinINSERM UMR-S1149/Center of Research on Inflammation (CRI), Université Paris Cité, Team "From Inflammation to Cancer in Digestive Diseases", DHU UNITY, Paris, France.
Inserm · FRCentre de Recherche sur l'Inflammation · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

At the end of the 20th century, two new neuropeptides (Orexin-A/hypocretin-1 and Orexin-B/hypocretins-2) expressed in hypothalamus as a prepro-orexins precursor, were discovered. These two neuropeptides interacted with two G protein-coupled receptor isoforms named OX1R and OX2R. The orexins/OX receptors system play an important role in the central and peripheral nervous system where it controls wakefulness, addiction, reward seeking, stress, motivation, memory, energy homeostasis, food intake, blood pressure, hormone secretions, reproduction, gut motility and lipolysis. Orexins and their receptors are involved in pathologies including narcolepsy type I, neuro- and chronic inflammation, neurodegenerative diseases, metabolic syndrome, and cancers. Associated with these physiopathological roles, the extensive development of pharmacological molecules including OXR antagonists, has emerged in association with the determination of the structural properties of orexins and their receptors. Moreover, the identification of OX1R expression in digestive cancers encompassing colon, pancreas and liver cancers and its ability to trigger mitochondrial apoptosis in tumoral cells, indicate a new putative therapeutical action of orexins and paradoxically OXR antagonists. The present review focuses on structural and anti-tumoral aspects of orexins and their receptors.

Indexed as

NeoplasmsNeuropeptidesHumansOrexin ReceptorsOrexinsReceptors, G-Protein-CoupledNeuropeptidesOrexin ReceptorsOrexinsReceptors, G-Protein-CoupledcancerG protein-coupled receptor(GPCR)Orexin receptorOrexinspharmacologyprotein structurestructure-function relationship

Identifiers

PMID35966051
PMCPMC9365956
OpenAlexW4288074597

What OpenQuestion 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 OpenQuestion graph.