Evidence map›Paper›PMID 31775252›Full record

ArticleMetabolites2019

ADGRL4/ELTD1 Silencing in Endothelial Cells Induces ACLY and SLC25A1 and Alters the Cellular Metabolic Profile.

David M Favara, Christos E Zois, Syed Haider, Elisabete Pires, Helen Sheldon, James McCullagh, Alison H Banham, Adrian L Harris

Open access · goldAbstract read
In one paragraph

Article in Metabolites, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

23 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Adhesion G protein-coupled receptors.Pharmacological reviews · 2026
    Review
  4. Article
  5. Article
  6. Review
  7. Structure of the GNature communications · 2025
    Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Animals : an open access journal from MDPI · 2021
    Article
  18. ELTD1-An Emerging Silent Actor in Cancer Drama Play.International journal of molecular sciences · 2021
    Review
  19. Article
  20. 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

8 authors at 2 institutions in 1 country.

David M FavaraBalliol College, University of Oxford, Oxford OX1 3BJ, UK.ORCID 0000-0003-3189-6658
Christos E ZoisDepartment of Oncology, University of Oxford, Oxford OX3 7DQ, UK.
Syed HaiderDepartment of Oncology, University of Oxford, Oxford OX3 7DQ, UK.ORCID 0000-0001-6685-5480
Elisabete PiresChemistry Research Laboratory, Department of Chemistry, University of Oxford, Oxford OX1 3TA, UK.
Helen SheldonDepartment of Oncology, University of Oxford, Oxford OX3 7DQ, UK.
James McCullaghChemistry Research Laboratory, Department of Chemistry, University of Oxford, Oxford OX1 3TA, UK.
Alison H BanhamNuffield Division of Clinical Laboratory Science, Radcliffe Department of Medicine, University of Oxford, Oxford OX3 9DU, UK.
Adrian L HarrisDepartment of Oncology, University of Oxford, Oxford OX3 7DQ, UK.ORCID 0000-0003-1376-8409
University of Oxford · GBInstitute of Cancer Research · GB

Funding

Cancer Research UK 10702Cancer Research UK 18974Cancer Research UK 21667Cancer Research UK C602/A18974
6 · The paper itself

Abstract

Adhesion G Protein-Coupled Receptor L4 (ADGRL4/ELTD1) is an endothelial cell adhesion G protein-coupled receptor (aGPCR) which regulates physiological and tumour angiogenesis, providing an attractive target for anti-cancer therapeutics. To date, ADGRL4/ELTD1's full role and mechanism of function within endothelial biology remains unknown, as do its ligand(s). In this study, ADGRL4/ELTD1 silencing, using two independent small interfering RNAs (siRNAs), was performed in human umbilical vein endothelial cells (HUVECS) followed by transcriptional profiling, target gene validation, and metabolomics using liquid chromatography-mass spectrometry in order to better characterise ADGRL4/ELTD1's role in endothelial cell biology. We show that ADGRL4/ELTD1 silencing induced expression of the cytoplasmic metabolic regulator ATP Citrate Lyase (ACLY) and the mitochondria-to-cytoplasm citrate transporter Solute Carrier Family 25 Member 1 (SLC25A1) but had no apparent effect on pathways downstream of ACLY (fatty acid and cholesterol synthesis or acetylation). Silencing induced KIT expression and affected the Notch signalling pathway, upregulating Delta Like Canonical Notch Ligand 4 (DLL4) and suppressing Jagged Canonical Notch Ligand 1 (

Indexed as

ADGRL4/ELTD1adhesion GPCRmetabolomics

Identifiers

PMID31775252
PMCPMC6950702
OpenAlexW2990831213

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.