Evidence mapPaperPMID 41748743Full record

ReviewNature reviews. Drug discovery2026

The therapeutic potential of orphan adhesion G-protein-coupled receptors.

Jin-Peng Sun, Peng Xiao, Ines Liebscher

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Drug discovery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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.

Jin-Peng SunNew Cornerstone Science Laboratory, Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Shandong University, Jinan, China. sunjinpeng@bjmu.edu.cn.ORCID http://orcid.org/0000-0003-3572-1580
Peng XiaoKey Department of Clinical Laboratory, The Second Hospital, Shandong University, Jinan, China.ORCID http://orcid.org/0000-0002-9809-3481
Ines LiebscherRudolf Schönheimer Institute of Biochemistry, Medical Faculty, Leipzig University, Leipzig, Germany. ines.liebscher@medizin.uni-leipzig.de.ORCID http://orcid.org/0000-0003-4480-8987

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adhesion G-protein-coupled receptors (aGPCRs) are essential membrane proteins that contribute to diverse human pathologies, including cancer, psychiatric disorders and autoimmune diseases. A defining feature of these receptors is the large N terminus including the GPCR autoproteolysis-inducing domain, which mediates autoproteolysis and enables complex modes of activation through both cis and trans signalling. Recent breakthroughs in structural biology, in particular, cryogenic electron microscopy structures of aGPCRs, have transformed our understanding of receptor activation and facilitated development of small-molecule agonists and antibody-based strategies, which hold considerable promise for therapeutic intervention. In this Review, we summarize the roles of aGPCRs in human disease and in phenotypes characterized in animal models. We consolidate current insights into aGPCR structure-function relationships, highlight how distinct activation mechanisms are already being harnessed to modulate receptor activity in vitro and in vivo, and discuss how these principles could be leveraged for future therapeutic targeting.

Indexed as

Receptors, G-Protein-CoupledAnimalsHumansNeoplasmsSignal TransductionStructure-Activity RelationshipReceptors, G-Protein-Coupled

Identifiers

What Socratic holds

Textmetadata
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.