Evidence map›Paper›PMID 35256936›Full record

ArticleActa pharmaceutica Sinica. B2022

Modulating effects of RAMPs on signaling profiles of the glucagon receptor family.

Lijun Shao, Yan Chen, Shikai Zhang, Zhihui Zhang, Yongbing Cao, Dehua Yang, Ming-Wei Wang

Open access · diamondAbstract read
In one paragraph

Article in Acta pharmaceutica Sinica. B, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

18 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Review
  3. Signaling architecture of the glucagon-like peptide-1 receptor.The Journal of clinical investigation · 2026
    Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Acta pharmaceutica Sinica. B · 2024
    Review
  14. Expanding the GPCR-RAMP interactome.bioRxiv : the preprint server for biology · 2023
    Article
  15. Molecular basis of signal transduction mediated by the human GIPR splice variants.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  16. Review
  17. Review
  18. 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 4 institutions in 1 country.

Lijun ShaoThe National Center for Drug Screening and CAS Key Laboratory of Receptor Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences (CAS), Shanghai 201203, China.
Yan ChenSchool of Pharmacy, Fudan University, Shanghai 201203, China.
Shikai ZhangShanghai TCM-Integrated Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 200082, China.
Zhihui ZhangShanghai TCM-Integrated Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 200082, China.
Yongbing CaoShanghai TCM-Integrated Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 200082, China.
Dehua YangThe National Center for Drug Screening and CAS Key Laboratory of Receptor Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences (CAS), Shanghai 201203, China.
Ming-Wei WangThe National Center for Drug Screening and CAS Key Laboratory of Receptor Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences (CAS), Shanghai 201203, China.
Shanghai University of Traditional Chinese Medicine · CNFudan University · CNShanghai Institute of Materia Medica · CNShanghaiTech University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Receptor activity-modulating proteins (RAMPs) are accessory molecules that form complexes with specific G protein-coupled receptors (GPCRs) and modulate their functions. It is established that RAMP interacts with the glucagon receptor family of GPCRs but the underlying mechanism is poorly understood. In this study, we used a bioluminescence resonance energy transfer (BRET) approach to comprehensively investigate such interactions. In conjunction with cAMP accumulation, G

Indexed as

Allosteric modulationAMY, amylinBmax, maximum measured BRET valueBRET, bioluminescence resonance energy transfercAMP, cyclic adenosine monophosphateCGRP, calcitonin gene-related peptideCLR, calcitonin-like receptorEC50, half maximal effective concentrationECD, extracellular domainEmax, maximal responseGCGR, glucagon receptorGHRHR, hormone-releasing hormone receptorGIPR, gastric inhibitory polypeptide receptor or glucose-dependent insulinotropic polypeptideGLP-1R, glucagon-like peptide-1 receptorGLP-2R, glucagon-like peptide-2 receptorGlucagon receptor familyGPCR–RAMP interactionGPCRs, G protein-coupled receptorsG protein-coupled receptorLigand selectivitypEC50, negative logarithm of EC50RAMP, receptor activity-modulating proteinReceptor activity-modulating proteinReceptor pharmacologyRluc, Renilla luciferaseSBA, suspension bead arraySCTR, secretin receptorSignalingSV, splice variantTMD, transmembrane domainVPAC2R, vasoactive intestinal polypeptide 2 receptorβ2-AR, β2-adrenergic receptor

Identifiers

PMID35256936
PMCPMC8897147
OpenAlexW3189733902

What OpenQuestion holds

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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.