Evidence map›Paper›PMID 26226451›Full record

ReviewJournal of hepatology2015

Emerging evidence on the role of the Hippo/YAP pathway in liver physiology and cancer.

Dean Yimlamai, Brendan H Fowl, Fernando D Camargo

Open access · greenAbstract readReview
In one paragraph

Review in Journal of hepatology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed
11.0field-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

99 citing papers in PubMed, 174 citations in OpenAlex.

  1. Article
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  10. Complex roles of Hippo-YAP/TAZ signaling in hepatocellular carcinoma.Journal of cancer research and clinical oncology · 2023
    Review
  11. Article
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  17. Review
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39 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.

Dean YimlamaiThe Stem Cell Program, Department of Medicine, Boston Children's Hospital, Boston, MA 02115, United States; Division of Gastroenterology and Nutrition, Department of Medicine, Boston Children's Hospital, Boston, MA 02115, United States. Electronic address: dean.yimlamai@childrens.harvard.edu.
Brendan H FowlThe Stem Cell Program, Department of Medicine, Boston Children's Hospital, Boston, MA 02115, United States; Division of Gastroenterology and Nutrition, Department of Medicine, Boston Children's Hospital, Boston, MA 02115, United States.
Fernando D CamargoThe Stem Cell Program, Department of Medicine, Boston Children's Hospital, Boston, MA 02115, United States; Harvard Stem Cell Institute, Cambridge, MA 02138, United States; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, United States. Electronic address: fernando.camargo@childrens.harvard.edu.
Boston Children's Hospital · US

Funding

STRUCTURE-FUNCTION RELATIONSHIPS IN THE ALIMENTARY TRACTP30DK034854 · NIDDK · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI LYNN BRY · 1986 to 2026
$32.4M
Hippo signaling and the control of epidermal development and growthR01AR064036 · NIAMS · BOSTON CHILDREN'S HOSPITAL · PI CAMARGO, FERNANDO · 2012 to 2016
$1.9M
Reprogramming of liver cell fate by Hippo signalingR01DK099559 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI CAMARGO, FERNANDO · 2013 to 2017
$1.9M
Hippo Signaling Mediates the Development of Liver FibrosisK08DK105351 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI YIMLAMAI, DEAN · 2015 to 2019
$796k
NIAMS NIH HHS R01 AR064036NIDDK NIH HHS K08 DK105351NIDDK NIH HHS P30 DK034854NIDDK NIH HHS R01 DK099559NIDDK NIH HHS R01 DK099559-01
6 · The paper itself

Abstract

The Hippo pathway and its regulatory target, YAP, has recently emerged as an important biochemical signaling pathway that tightly governs epithelial tissue growth. Initially defined in Drosophilia, this pathway has shown remarkable conservation in vertebrate systems with many components of the Hippo/YAP pathway showing biochemical and functional conservation. The liver is particularly sensitive to changes in Hippo/YAP signaling with rapid increases in liver size becoming manifest on the order of days to weeks after perturbation. The first identified direct targets of Hippo/YAP signaling were pro-proliferative and anti-apoptotic gene programs, but recent work has now implicated this pathway in cell fate choice, stem cell maintenance/renewal, epithelial to mesenchymal transition, and oncogenesis. The mechanisms by which Hippo/YAP signaling is changed endogenously are beginning to come to light as well as how this pathway interacts with other signaling pathways, and important details for designing new therapeutic interventions. This review focuses on the known roles for Hippo/YAP signaling in the liver and promising avenues for future study.

Indexed as

AnimalsDrosophila ProteinsHippo KinasesHumansIntracellular Signaling Peptides and ProteinsLiverLiver NeoplasmsLiver RegenerationModels, BiologicalNuclear ProteinsOrgan SizeProtein Serine-Threonine KinasesSignal TransductionTrans-ActivatorsYAP-Signaling ProteinsDrosophila ProteinsHippo Kinaseshpo protein, DrosophilaIntracellular Signaling Peptides and ProteinsNuclear ProteinsProtein Serine-Threonine KinasesTrans-ActivatorsYAP-Signaling ProteinsYki protein, DrosophilaHippo signalingLiver regenerationStem cell biology

Identifiers

PMID26226451
PMCPMC4654680
OpenAlexW1955705095

What OpenQuestion holds

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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.