Evidence map›Paper›PMID 30948712›Full record

ArticleNature communications2019

Identification of the kinase STK25 as an upstream activator of LATS signaling.

Sanghee Lim, Nicole Hermance, Tenny Mudianto, Hatim M Mustaly, Ian Paolo Morelos Mauricio, Marc A Vittoria, Ryan J Quinton, Brian W Howell, Hauke Cornils, Amity L Manning and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

33 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
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  7. Review
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  9. Targeting the Hippo pathway in heart repair.Cardiovascular research · 2022
    Review
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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

11 authors at 4 institutions in 2 countries.

Sanghee LimThe Laboratory of Cancer Cell Biology, Department of Pharmacology and Experimental Therapeutics, Boston University School of Medicine, Boston, MA, 02118, USA.
Nicole HermanceDepartment of Biology and Biotechnology, Worcester Polytechnic Institute, Worcester, MA, 01605, USA.
Tenny MudiantoThe Laboratory of Cancer Cell Biology, Department of Pharmacology and Experimental Therapeutics, Boston University School of Medicine, Boston, MA, 02118, USA.
Hatim M MustalyThe Laboratory of Cancer Cell Biology, Department of Pharmacology and Experimental Therapeutics, Boston University School of Medicine, Boston, MA, 02118, USA.
Ian Paolo Morelos MauricioThe Laboratory of Cancer Cell Biology, Department of Pharmacology and Experimental Therapeutics, Boston University School of Medicine, Boston, MA, 02118, USA.
Marc A VittoriaThe Laboratory of Cancer Cell Biology, Department of Pharmacology and Experimental Therapeutics, Boston University School of Medicine, Boston, MA, 02118, USA.
Ryan J QuintonThe Laboratory of Cancer Cell Biology, Department of Pharmacology and Experimental Therapeutics, Boston University School of Medicine, Boston, MA, 02118, USA.
Brian W HowellDepartment of Neuroscience and Physiology, SUNY Upstate Medical University, Syracuse, NY, 13210, USA.ORCID http://orcid.org/0000-0002-0204-0773
Hauke CornilsEvotec, Hamburg, 22419, Germany.
Amity L ManningDepartment of Biology and Biotechnology, Worcester Polytechnic Institute, Worcester, MA, 01605, USA.
Neil J GanemThe Laboratory of Cancer Cell Biology, Department of Pharmacology and Experimental Therapeutics, Boston University School of Medicine, Boston, MA, 02118, USA. nganem@bu.edu.
Boston University · USWorcester Polytechnic Institute · USEvotec (Germany) · DESUNY Upstate Medical University · US

Funding

Project-005UL1TR001430 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BAIR-MERRITT, MEGAN H, CENTER, DAVID M. · 2015 to 2024
$52.3M
TRAINING IN BIOMOLECULAR PHARMACOLOGYT32GM008541 · NIGMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI FARB, DAVID H · 1997 to 2022
$5.2M
Regulation of cell growth and proliferation by the Hippo pathwayR01GM117150 · NIGMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI NEIL J. GANEM · 2016 to 2026
$2.4M
Regulation of Neuronal Lamination and Dendritogenesis by Reelin-Dab1 SignalingR01NS073662 · NINDS · UPSTATE MEDICAL UNIVERSITY · PI HOWELL, BRIAN W. · 2011 to 2015
$1.7M
Manipulating chromosome structure to suppress genome instabilityR00CA182731 · NCI · WORCESTER POLYTECHNIC INSTITUTE · PI MANNING, AMITY · 2015 to 2017
$747k
Defining novel pathways that arrest genetically unstable tetraploid cellsR00CA154531 · NCI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI GANEM, NEIL J. · 2013 to 2015
$723k
Defining novel pathways that arrest genetically unstable tetraploid cellsK99CA154531 · NCI · DANA-FARBER CANCER INST · PI GANEM, NEIL J. · 2011 to 2012
$300k
Defining Novel Mechanisms of Genome Instability in BRAF-mutant MelanomaF30CA228388 · NCI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI VITTORIA, MARC ANTHONY · 2018 to 2022
$253k
NCATS NIH HHS UL1 TR001430NCI NIH HHS F30 CA228388NCI NIH HHS K99 CA154531NCI NIH HHS R00 CA154531NCI NIH HHS R00 CA182731NIGMS NIH HHS R01 GM117150NIGMS NIH HHS T32 GM008541NINDS NIH HHS R01 NS073662
6 · The paper itself

Abstract

The Hippo pathway maintains tissue homeostasis by negatively regulating the oncogenic transcriptional co-activators YAP and TAZ. Though functional inactivation of the Hippo pathway is common in tumors, mutations in core pathway components are rare. Thus, understanding how tumor cells inactivate Hippo signaling remains a key unresolved question. Here, we identify the kinase STK25 as an activator of Hippo signaling. We demonstrate that loss of STK25 promotes YAP/TAZ activation and enhanced cellular proliferation, even under normally growth-suppressive conditions both in vitro and in vivo. Notably, STK25 activates LATS by promoting LATS activation loop phosphorylation independent of a preceding phosphorylation event at the hydrophobic motif, which represents a form of Hippo activation distinct from other kinase activators of LATS. STK25 is significantly focally deleted across a wide spectrum of human cancers, suggesting STK25 loss may represent a common mechanism by which tumor cells functionally impair the Hippo tumor suppressor pathway.

Indexed as

Gene Expression Regulation, NeoplasticCell LineCell ProliferationGenes, Tumor SuppressorHippo KinasesHippo Signaling PathwayHumansIntracellular Signaling Peptides and ProteinsProtein Serine-Threonine KinasesSignal TransductionHippo KinasesIntracellular Signaling Peptides and ProteinsProtein Serine-Threonine KinasesSTK25 protein, human

Identifiers

PMID30948712
PMCPMC6449379
OpenAlexW2930356180

What OpenQuestion holds

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Registered trials

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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.