Evidence map›Paper›PMID 39051998›Full record

ArticleeLife2024

Hippo pathway-mediated YAP1/TAZ inhibition is essential for proper pancreatic endocrine specification and differentiation.

Yifan Wu, Kunhua Qin, Yi Xu, Shreya Rajhans, Truong Vo, Kevin M Lopez, Jun Liu, Michael H Nipper, Janice Deng, Xue Yin and 5 more

Abstract read
In one paragraph

Article in eLife, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Review
  2. Article
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  5. 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

15 authors.

Yifan Wu *Department of Cell Systems & Anatomy, University of Texas Health Science Center at San Antonio, San Antonio, United States.ORCID https://orcid.org/0000-0002-8124-8651
Kunhua Qin *Department of Cell Systems & Anatomy, University of Texas Health Science Center at San Antonio, San Antonio, United States.
Yi XuDepartment of Cell Systems & Anatomy, University of Texas Health Science Center at San Antonio, San Antonio, United States.
Shreya RajhansLaboratory of Receptor Biology and Gene Expression, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, United States.
Truong VoLaboratory of Receptor Biology and Gene Expression, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, United States.
Kevin M LopezDepartment of Cell Systems & Anatomy, University of Texas Health Science Center at San Antonio, San Antonio, United States.ORCID https://orcid.org/0000-0002-3163-4634
Jun LiuDepartment of Cell Systems & Anatomy, University of Texas Health Science Center at San Antonio, San Antonio, United States.
Michael H NipperDepartment of Cell Systems & Anatomy, University of Texas Health Science Center at San Antonio, San Antonio, United States.
Janice DengDepartment of Cell Systems & Anatomy, University of Texas Health Science Center at San Antonio, San Antonio, United States.
Xue YinDepartment of Cell Systems & Anatomy, University of Texas Health Science Center at San Antonio, San Antonio, United States.
Logan R RamjitDepartment of Cell Systems & Anatomy, University of Texas Health Science Center at San Antonio, San Antonio, United States.
Zhenqing YeDepartment of Population Health Sciences, University of Texas Health Science Center at San Antonio, San Antonio, United States.
Yu LuanDepartment of Cell Systems & Anatomy, University of Texas Health Science Center at San Antonio, San Antonio, United States.
H Efsun ArdaLaboratory of Receptor Biology and Gene Expression, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, United States.ORCID https://orcid.org/0000-0002-5294-2521
Pei WangDepartment of Cell Systems & Anatomy, University of Texas Health Science Center at San Antonio, San Antonio, United States.ORCID https://orcid.org/0000-0003-2373-7315

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Robin Jean Leach · 1991 to 2026
$59.1M
Identification of genomic regulatory elements in pancreas cellsZIABC011798 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI ARDA, HATICE · 2018 to 2025
$10.5M
Mechanisms of pancreatic cancer initiation and progression from normal human pancreatic tissueR01CA237159 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI WANG, PEI · 2020 to 2025
$1.7M
The Hippo signaling pathway in pancreatic epithelial cells orchestrate the inflammatory response R01R01DK110361 · NIDDK · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI WANG, PEI · 2017 to 2021
$1.7M
Novel model to study PDAC using normal human pancreatic tissueR21CA218968 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI WANG, PEI · 2017 to 2018
$365k
Cancer Prevention and Research Institute of Texas R1219Cancer Prevention and Research Institute of Texas RP170345CPRIT Research Training RP140105Intramural NIH HHS ZIA BC011798NCI NIH HHS P30 CA054174NCI NIH HHS R01 CA237159NCI NIH HHS R21 CA218968NIDDK NIH HHS R01 DK110361NIDDK NIH HHS R01DK110361
6 · The paper itself

Abstract

The Hippo pathway plays a central role in tissue development and homeostasis. However, the function of Hippo in pancreatic endocrine development remains obscure. Here, we generated novel conditional genetically engineered mouse models to examine the roles of Hippo pathway-mediated YAP1/TAZ inhibition in the development stages of endocrine specification and differentiation. While YAP1 protein was localized to the nuclei in bipotent progenitor cells, Neurogenin 3 expressing endocrine progenitors completely lost YAP1 expression. Using genetically engineered mouse models, we found that inactivation of YAP1 requires both an intact Hippo pathway and Neurogenin 3 protein. Gene deletion of Lats1 and 2 kinases (

Indexed as

Adaptor Proteins, Signal TransducingCell DifferentiationProtein Serine-Threonine KinasesSignal TransductionYAP-Signaling ProteinsAcyltransferasesAnimalsBasic Helix-Loop-Helix ProteinsCell Cycle ProteinsHippo Signaling PathwayIslets of LangerhansMiceNerve Tissue ProteinsPhosphoproteinsTrans-ActivatorsTranscriptional Coactivator with PDZ-Binding Motif ProteinsAcyltransferasesAdaptor Proteins, Signal TransducingBasic Helix-Loop-Helix ProteinsCell Cycle ProteinsLats1 protein, mouseLATS2 protein, mouseNerve Tissue ProteinsNeurog3 protein, mousePhosphoproteinsProtein Serine-Threonine Kinasestafazzin protein, mouseTrans-ActivatorsTranscriptional Coactivator with PDZ-Binding Motif ProteinsTranscription FactorsTumor Suppressor ProteinsWwtr1 protein, mouseYap1 protein, mouseYAP-Signaling Proteinsdevelopmentdevelopmental biologydifferentiationendocrine progenitorsHippo signalingmousepancreasspecification

Identifiers

PMID39051998
PMCPMC11272159

What Socratic 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 Socratic graph.