Evidence map›Paper›PMID 31857346›Full record

ArticleGenes & development2020

CDK7 regulates organ size and tumor growth by safeguarding the Hippo pathway effector Yki/Yap/Taz in the nucleus.

Yong Suk Cho, Shuang Li, Xiaohui Wang, Jian Zhu, Shu Zhuo, Yuhong Han, Tao Yue, Yingzi Yang, Jin Jiang

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing 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

47 citing papers in PubMed, 60 citations in OpenAlex.

  1. Review
  2. Yorkie/YAP Interactors: Fine-Tuning the Hippo Pathway Output.Cold Spring Harbor perspectives in biology · 2026
    Article
  3. Review
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  10. Review
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  13. CDK9 Inhibition by Dinaciclib Is a Therapeutic Vulnerability in Epithelioid Hemangioendothelioma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Yong Suk Cho *Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Shuang Li *Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Xiaohui WangDepartment of Developmental Biology, Harvard School of Dental Medicine, Boston, Massachusetts 02215, USA.
Jian ZhuDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Shu ZhuoDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Yuhong HanDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Tao YueCenter for the Genetics and Host Defense, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Yingzi YangDepartment of Developmental Biology, Harvard School of Dental Medicine, Boston, Massachusetts 02215, USA.
Jin JiangDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
The University of Texas Southwestern Medical Center · USHarvard Stem Cell Institute · USHarvard University · US

Funding

Cell signaling in development and regenerationR35GM118063 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI Jin Jiang · 2016 to 2026
$9.4M
Cellular and molecular mechanism of Hippo signaling in suppressing liver tumor formationR01CA222571 · NCI · HARVARD MEDICAL SCHOOL · PI YANG, YINGZI · 2018 to 2022
$1.9M
NCI NIH HHS R01 CA222571NIGMS NIH HHS R35 GM118063
6 · The paper itself

Abstract

Hippo signaling controls organ size and tumor progression through a conserved pathway leading to nuclear translocation of the transcriptional effector Yki/Yap/Taz. Most of our understanding of Hippo signaling pertains to its cytoplasmic regulation, but how the pathway is controlled in the nucleus remains poorly understood. Here we uncover an evolutionarily conserved mechanism by which CDK7 promotes Yki/Yap/Taz stabilization in the nucleus to sustain Hippo pathway outputs. We found that a modular E3 ubiquitin ligase complex CRL4

Indexed as

AnimalsAntineoplastic AgentsCarcinogenesisCell LineCell Line, TumorCell NucleusCyclin-Dependent Kinase-Activating KinaseCyclin-Dependent KinasesDrosophila melanogasterDrosophila ProteinsEnzyme ActivationGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumansLiver NeoplasmsMiceAntineoplastic AgentsCyclin-Dependent Kinase-Activating KinaseCyclin-Dependent KinasesDis3 protein, DrosophilaDrosophila ProteinsNuclear ProteinsPhenylenediaminesPyrimidinesTHZ1 compoundTrans-ActivatorsYAP-Signaling ProteinsYki protein, DrosophilacancerCDK7CRL4Cul4DCAF12Hippoorgan sizeTazYapYki

Identifiers

PMID31857346
PMCPMC6938674
OpenAlexW2995406658

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.