Evidence map›Paper›PMID 36677809›Full record

ReviewMolecules (Basel, Switzerland)2023

GLP-1R Signaling and Functional Molecules in Incretin Therapy.

Wenwei Wan, Qikai Qin, Linshan Xie, Hanqing Zhang, Fan Wu, Raymond C Stevens, Yan Liu

Open access · goldAbstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
6.8field-weighted citation impact, top 2% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Glucagon-like peptide-1 receptor: mechanisms and advances in therapy.Signal transduction and targeted therapy · 2024 · on this map
    Review
  9. Review
  10. Article
  11. Cryo-electron microscopy-based drug design.Frontiers in molecular biosciences · 2024
    Review
  12. Review
  13. Article
  14. Article
  15. The foot in diabetes - a reminder of an ever-present risk.Clinical medicine (London, England) · 2023
    Review
  16. 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

7 authors at 1 institution in 1 country.

Wenwei WaniHuman Institute, ShanghaiTech University, School of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China.
Qikai QiniHuman Institute, ShanghaiTech University, School of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China.ORCID 0000-0002-8826-5171
Linshan XieiHuman Institute, ShanghaiTech University, School of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China.ORCID 0000-0002-2890-1703
Hanqing ZhangiHuman Institute, ShanghaiTech University, Shanghai 201210, China.ORCID 0000-0003-3888-3737
Fan WuStructure Therapeutics, South San Francisco, CA 94080, USA.
Raymond C StevensiHuman Institute, ShanghaiTech University, Shanghai 201210, China.
Yan LiuiHuman Institute, ShanghaiTech University, Shanghai 201210, China.ORCID 0000-0002-7682-3498
ShanghaiTech University · CN

Funding

Science and Technology Commission of Shanghai Municipality 21ZR1442500Shanghai Frontiers Science Center for Biomacromolecules and Precision Medicine at ShanghaiTech University NAShanghai Municipal Government NAShanghaiTech University NA
6 · The paper itself

Abstract

Glucagon-like peptide-1 receptor (GLP-1R) is a critical therapeutic target for type 2 diabetes mellitus (T2DM). The GLP-1R cellular signaling mechanism relevant to insulin secretion and blood glucose regulation has been extensively studied. Numerous drugs targeting GLP-1R have entered clinical treatment. However, novel functional molecules with reduced side effects and enhanced therapeutic efficacy are still in high demand. In this review, we summarize the basis of GLP-1R cellular signaling, and how it is involved in the treatment of T2DM. We review the functional molecules of incretin therapy in various stages of clinical trials. We also outline the current strategies and emerging techniques that are furthering the development of novel therapeutic drugs for T2DM and other metabolic diseases.

Indexed as

Diabetes Mellitus, Type 2IncretinsGlucagon-Like Peptide-1 ReceptorHumansInsulinSignal TransductionGlucagon-Like Peptide-1 ReceptorIncretinsInsulindrug discoveryfunctional moleculesGLP-1R signalingincretin therapytype 2 diabetes mellitus

Identifiers

PMID36677809
PMCPMC9866634
OpenAlexW4315781708

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.