Evidence map›Paper›PMID 29535383›Full record

ArticleNature communications2018

A LATS biosensor screen identifies VEGFR as a regulator of the Hippo pathway in angiogenesis.

T Azad, H J Janse van Rensburg, E D Lightbody, B Neveu, A Champagne, A Ghaffari, V R Kay, Y Hao, H Shen, B Yeung and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 108 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
108citing papers in PubMed, 1 pooled it
10.2field-weighted citation impact, top 1% 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

108 citing papers in PubMed, 1 synthesis or guideline pooled it, 164 citations in OpenAlex.

  1. The Hippo signalling pathway and its impact on eye diseases.Journal of cellular and molecular medicine · 2024
    Pooled it
  2. Review
  3. Article
  4. The kidney stroma in development and disease.Nature reviews. Nephrology · 2025
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Luciferase complementation for cellular assays beyond protein-protein interactions.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2025
    Review
  12. Article
  13. Review
  14. Review
  15. Observational
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article

48 more citing papers are in PubMed but not listed here.

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

16 authors at 4 institutions in 2 countries.

T AzadDepartment of Pathology and Molecular Medicine, Queen's University, Kingston, Ontario, Canada, K7L3N6.
H J Janse van RensburgDepartment of Pathology and Molecular Medicine, Queen's University, Kingston, Ontario, Canada, K7L3N6.
E D LightbodyDepartment of Pathology and Molecular Medicine, Queen's University, Kingston, Ontario, Canada, K7L3N6.
B NeveuDepartment of Surgery (Urology), CHU de Québec-Université Laval Research Center, Laval University, Quebec, Ontario, Canada, G1V 0A6.
A ChampagneDepartment of Surgery (Urology), CHU de Québec-Université Laval Research Center, Laval University, Quebec, Ontario, Canada, G1V 0A6.ORCID http://orcid.org/0000-0002-2828-5381
A GhaffariDepartment of Pathology and Molecular Medicine, Queen's University, Kingston, Ontario, Canada, K7L3N6.
V R KayDepartment of Biomedical and Molecular Sciences, Queen's University, Kingston, Ontario, Canada, K7L 3N6.
Y HaoDepartment of Pathology and Molecular Medicine, Queen's University, Kingston, Ontario, Canada, K7L3N6.
H ShenDepartment of Cancer Genetics and Genomics, Roswell Park Cancer Institute, Buffalo, NY, 14263, USA.
B YeungDepartment of Pathology and Molecular Medicine, Queen's University, Kingston, Ontario, Canada, K7L3N6.
B A CroyDepartment of Biomedical and Molecular Sciences, Queen's University, Kingston, Ontario, Canada, K7L 3N6.ORCID http://orcid.org/0000-0002-1866-3270
K L GuanDepartment of Pharmacology, University of California at San Diego, La Jolla, CA, 92093, USA.ORCID http://orcid.org/0000-0003-1892-0174
F PouliotDepartment of Surgery (Urology), CHU de Québec-Université Laval Research Center, Laval University, Quebec, Ontario, Canada, G1V 0A6.
J ZhangDepartment of Cancer Genetics and Genomics, Roswell Park Cancer Institute, Buffalo, NY, 14263, USA.
C J B NicolDepartment of Pathology and Molecular Medicine, Queen's University, Kingston, Ontario, Canada, K7L3N6.
X YangDepartment of Pathology and Molecular Medicine, Queen's University, Kingston, Ontario, Canada, K7L3N6. yangx@queensu.ca.
Queen's University · CAUniversité Laval · CARoswell Park Comprehensive Cancer Center · USUniversity of California San Diego · US

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MARK G FRATTINI · 1985 to 2026
$116.6M
The mTOR and Hippo pathway in cell growth and cancerR35CA196878 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GUAN, KUN-LIANG · 2015 to 2019
$4.0M
The role of TAZ in breast cancer initiation and progressionR01CA207504 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI ZHANG, JIANMIN · 2017 to 2021
$2.0M
Hippo signaling pathway in breast cancer disparities: a translational approachR21CA179693 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI ZHANG, JIANMIN · 2014 to 2015
$615k
NCI NIH HHS P30 CA016056NCI NIH HHS R01 CA207504NCI NIH HHS R21 CA179693NCI NIH HHS R35 CA196878
6 · The paper itself

Abstract

The Hippo pathway is a central regulator of tissue development and homeostasis, and has been reported to have a role during vascular development. Here we develop a bioluminescence-based biosensor that monitors the activity of the Hippo core component LATS kinase. Using this biosensor and a library of small molecule kinase inhibitors, we perform a screen for kinases modulating LATS activity and identify VEGFR as an upstream regulator of the Hippo pathway. We find that VEGFR activation by VEGF triggers PI3K/MAPK signaling, which subsequently inhibits LATS and activates the Hippo effectors YAP and TAZ. We further show that the Hippo pathway is a critical mediator of VEGF-induced angiogenesis and tumor vasculogenic mimicry. Thus, our work offers a biosensor tool for the study of the Hippo pathway and suggests a role for Hippo signaling in regulating blood vessel formation in physiological and pathological settings.

Indexed as

Biosensing TechniquesA549 CellsAdaptor Proteins, Signal TransducingAnimalsBlotting, WesternFemaleHEK293 CellsHumansImmunohistochemistryMutagenesis, Site-DirectedPhosphatidylinositol 3-KinasesPhosphoproteinsProtein Serine-Threonine KinasesReceptors, Vascular Endothelial Growth FactorSignal TransductionTranscription FactorsAdaptor Proteins, Signal TransducingLATS2 protein, humanPhosphatidylinositol 3-KinasesPhosphoproteinsProtein Serine-Threonine KinasesReceptors, Vascular Endothelial Growth FactorTranscription FactorsTumor Suppressor Proteins

Identifiers

PMID29535383
PMCPMC5849716
OpenAlexW2793818146

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.