Evidence map›Paper›PMID 30183404›Full record

ReviewAnnual review of genetics2018

The Hippo Signaling Network and Its Biological Functions.

Jyoti R Misra, Kenneth D Irvine

Abstract readReview
In one paragraph

Review in Annual review of genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 291 papers.

0numbers the graph read from it
0cells of the map it votes in
291citing papers in PubMed
21.6field-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

291 citing papers in PubMed, 539 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Homer condensates orchestrate YAP-Wnt signaling crosstalk downstream of the Crumbs polarity complex.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Mechanobiology of the Hippo-YAP Signaling Network.Cold Spring Harbor perspectives in biology · 2026
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

231 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

2 authors at 1 institution in 1 country.

Jyoti R MisraWaksman Institute and Department of Molecular Biology and Biochemistry, Rutgers University, Piscataway, New Jersey 08854, USA; email: irvine@waksman.rutgers.edu.
Kenneth D IrvineWaksman Institute and Department of Molecular Biology and Biochemistry, Rutgers University, Piscataway, New Jersey 08854, USA; email: irvine@waksman.rutgers.edu.
Rutgers, The State University of New Jersey · US

Funding

Growth regulation by the Fat signaling pathwayR01GM078620 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI IRVINE, KENNETH D · 2007 to 2018
$3.3M
Biomechanical Regulation of Organ GrowthR01GM121537 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI IRVINE, KENNETH D · 2017 to 2019
$1.3M
Regulation of organ size and shape by Fat signalingK99HD092553 · NICHD · RUTGERS, THE STATE UNIV OF N.J. · PI MISRA, JYOTI R. · 2017 to 2018
$219k
NICHD NIH HHS K99 HD092553NIGMS NIH HHS R01 GM078620NIGMS NIH HHS R01 GM121537
6 · The paper itself

Abstract

Hippo signaling is an evolutionarily conserved network that has a central role in regulating cell proliferation and cell fate to control organ growth and regeneration. It promotes activation of the LATS kinases, which control gene expression by inhibiting the activity of the transcriptional coactivator proteins YAP and TAZ in mammals and Yorkie in Drosophila. Diverse upstream inputs, including both biochemical cues and biomechanical cues, regulate Hippo signaling and enable it to have a key role as a sensor of cells' physical environment and an integrator of growth control signals. Several components of this pathway localize to cell-cell junctions and contribute to regulation of Hippo signaling by cell polarity, cell contacts, and the cytoskeleton. Downregulation of Hippo signaling promotes uncontrolled cell proliferation, impairs differentiation, and is associated with cancer. We review the current understanding of Hippo signaling and highlight progress in the elucidation of its regulatory mechanisms and biological functions.

Indexed as

AcyltransferasesAdaptor Proteins, Signal TransducingAnimalsCell CommunicationCell Cycle ProteinsCell MovementCell PolarityCell ProliferationCytoskeletonDrosophilaDrosophila ProteinsGene Expression RegulationHippo Signaling PathwayHumansIntercellular JunctionsMiceAcyltransferasesAdaptor Proteins, Signal TransducingCell Cycle ProteinsDrosophila ProteinsNuclear ProteinsPhosphoproteinsProtein Serine-Threonine KinasesTAFAZZIN protein, humanTrans-ActivatorsTranscription FactorsYap1 protein, mouseYAP-Signaling ProteinsYki protein, DrosophilacancergrowthHippoYAPYorkie

Identifiers

PMID30183404
PMCPMC6322405
OpenAlexW2891780076

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.