Evidence map›Paper›PMID 25702974›Full record

ReviewTrends in molecular medicine2015

Disease implications of the Hippo/YAP pathway.

Steven W Plouffe, Audrey W Hong, Kun-Liang Guan

Open access · greenAbstract readReview
In one paragraph

Review in Trends in molecular medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 141 papers.

0numbers the graph read from it
0cells of the map it votes in
141citing papers in PubMed
12.7field-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

141 citing papers in PubMed, 236 citations in OpenAlex.

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  18. Unraveling the Antioxidant Capacity ofAntioxidants (Basel, Switzerland) · 2023
    Article
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81 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

3 authors at 1 institution in 1 country.

Steven W PlouffeDepartment of Pharmacology, University of California, San Diego, La Jolla, CA, USA; Moores Cancer Center, University of California, San Diego, La Jolla, CA, USA.
Audrey W HongDepartment of Pharmacology, University of California, San Diego, La Jolla, CA, USA; Moores Cancer Center, University of California, San Diego, La Jolla, CA, USA.
Kun-Liang GuanDepartment of Pharmacology, University of California, San Diego, La Jolla, CA, USA; Moores Cancer Center, University of California, San Diego, La Jolla, CA, USA. Electronic address: kuguan@ucsd.edu.
University of California, San Diego · US

Funding

VIRAL MALIGNANCYP30CA023100 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Jesse Nodora · 1985 to 2026
$124.9M
GRADUATE TRAINING IN CELLULAR &MOLECULAR PHARMACOLOGYT32GM007752 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BROWN, JOAN HELLER, HANDEL, TRACY M · 1985 to 2023
$13.5M
TSC2 tumor suppressor protein in cell energy responseR01CA108941 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GUAN, KUN-LIANG · 2004 to 2015
$3.8M
Regulation and function of the YAP transcription co-activator oncoproteinR01CA132809 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GUAN, KUN-LIANG · 2008 to 2015
$2.6M
Regulation of the Hippo pathway and its role in uveal melanomaR01EY022611 · NEI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GUAN, KUN-LIANG · 2012 to 2015
$1.5M
NCI NIH HHS CA132809NCI NIH HHS P30 CA023100NCI NIH HHS P30CA023100NCI NIH HHS R01 CA108941NCI NIH HHS R01 CA132809NEI NIH HHS R01 EY022611NIGMS NIH HHS T32 GM007752PHS HHS EYO226116
6 · The paper itself

Abstract

The Hippo signaling pathway is important for controlling organ size and tissue homeostasis. Originally identified in Drosophila melanogaster, the core components of the Hippo pathway are highly conserved in mammals. The Hippo pathway can be modulated by a wide range of stimuli, including G protein-coupled receptor (GPCR) signaling, changes in the actin cytoskeleton, cell-cell contact, and cell polarity. When activated, the Hippo pathway functions as a tumor suppressor to limit cell growth. However, dysregulation by genetic inactivation of core pathway components or amplification or gene fusion of its downstream effectors results in increased cell proliferation and decreased apoptosis and differentiation. Unsurprisingly, this can lead to tissue overgrowth, tumorigenesis, and many other diseases.

Indexed as

Signal TransductionAnimalsApoptosisCarcinogenesisCell ProliferationDrosophila melanogasterDrosophila ProteinsGene Expression Regulation, DevelopmentalGene Expression Regulation, NeoplasticHippo KinasesHippo Signaling PathwayHomeostasisHumansIntracellular Signaling Peptides and ProteinsMammalsNeoplasmsDrosophila ProteinsHippo Kinaseshpo protein, DrosophilaIntracellular Signaling Peptides and ProteinsNuclear ProteinsProtein Serine-Threonine KinasesReceptors, G-Protein-CoupledTrans-ActivatorsTranscription FactorsYAP-Signaling ProteinsYki protein, DrosophilacancerdiseaseHippoTAZYAP

Identifiers

PMID25702974
PMCPMC4385444
OpenAlexW2060070915

What OpenQuestion holds

Textmetadata
LicenceTDM
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.