Evidence map›Paper›PMID 41469374›Full record

ArticleNature communications2025

Structure of the G

Qingchao Chen, Anastasiia Gusach, Aurora Diamante, Jayesh C Patel, Patricia C Edwards, Christopher G Tate, David M Favara

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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.

Qingchao ChenMRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, UK.
Anastasiia GusachMRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, UK.ORCID http://orcid.org/0000-0002-2594-8573
Aurora DiamanteNxera Pharma UK Limited, Steinmetz Building, Granta Park, Great Abington, Cambridge, UK.
Jayesh C PatelNxera Pharma UK Limited, Steinmetz Building, Granta Park, Great Abington, Cambridge, UK.
Patricia C EdwardsMRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, UK.
Christopher G TateMRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, UK.ORCID http://orcid.org/0000-0002-2008-9183
David M FavaraMRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, UK. dfavara@mrc-lmb.cam.ac.uk.ORCID http://orcid.org/0000-0003-3189-6658

Funding

Cancer Research UK (CRUK) RCCPOB-May22\100008RCUK | Medical Research Council (MRC) MRC U105197215
6 · The paper itself

Abstract

Adhesion G protein-coupled receptors (aGPCRs) are a 32-member family of Class B GPCRs that have diverse cellular roles including mechanosensation, cell-fate determination, neurodevelopment, immune function and tumour biology. ADGRL4 is upregulated in the tumour microenvironment and is implicated in tumour pathogenesis across a broad range of malignancies. Inhibiting ADGRL4 is a potential therapeutic treatment for currently intractable cancers such as glioblastoma. Previous work suggested that ADGRL4 does not signal through G protein coupled pathways. However, using a sensitive bioluminescent assay, we demonstrate here that ADGRL4 couples weakly to the heterotrimeric G protein G

Indexed as

GTP-Binding Protein alpha Subunits, Gq-G11Receptors, G-Protein-CoupledCryoelectron MicroscopyHEK293 CellsHumansProtein BindingGTP-Binding Protein alpha Subunits, Gq-G11Receptors, G-Protein-Coupled

Identifiers

PMID41469374
PMCPMC12830901

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.