Evidence map›Paper›PMID 32269044›Full record

ArticleCancer research2020

EIF3H Orchestrates Hippo Pathway-Mediated Oncogenesis via Catalytic Control of YAP Stability.

Zhuan Zhou, Honghong Zhou, Luca Ponzoni, Aiping Luo, Rui Zhu, Mingjing He, Yi Huang, Kun-Liang Guan, Ivet Bahar, Zhihua Liu and 1 more

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

29 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. mFrontiers in cell and developmental biology · 2026
    Review
  5. Targeting ubiquitination in disease and therapy.Signal transduction and targeted therapy · 2025
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
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  13. Article
  14. Article
  15. Unraveling the therapeutic potential ofIn silico pharmacology · 2024
    Article
  16. Review
  17. Article
  18. Article
  19. Comparative Ubiquitome Analysis Reveals Deubiquitinating Effects Induced byInternational journal of molecular sciences · 2022
    Article
  20. Structural basis and molecular mechanism of biased GPBAR signaling in regulating NSCLC cell growth via YAP activity.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
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

11 authors at 5 institutions in 2 countries.

Zhuan Zhou *Department of Obstetrics and Gynecology, Department of Pharmacology, The Robert H. Lurie Comprehensive Cancer Center, Chemical of Life Processes Institute, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Honghong Zhou *State Key Laboratory of Molecular Oncology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Luca Ponzoni *Department of Computational and Systems Biology, University of Pittsburgh School of Medicine, Pennsylvania.ORCID 0000-0001-8125-582X
Aiping LuoState Key Laboratory of Molecular Oncology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Rui ZhuState Key Laboratory of Molecular Oncology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Mingjing HeUPMC Hillman Cancer Center, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Yi HuangUPMC Hillman Cancer Center, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Kun-Liang GuanDepartment of Pharmacology, Moores Cancer Center, University of California at San Diego, La Jolla, California.ORCID 0000-0003-1892-0174
Ivet BaharDepartment of Computational and Systems Biology, University of Pittsburgh School of Medicine, Pennsylvania.ORCID 0000-0001-9959-4176
Zhihua LiuState Key Laboratory of Molecular Oncology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China. yong.wan@northwestern.edu liuzh@cicams.ac.cn.
Yong WanDepartment of Obstetrics and Gynecology, Department of Pharmacology, The Robert H. Lurie Comprehensive Cancer Center, Chemical of Life Processes Institute, Northwestern University Feinberg School of Medicine, Chicago, Illinois. yong.wan@northwestern.edu liuzh@cicams.ac.cn.
Chinese Academy of Medical Sciences & Peking Union Medical College · CNRobert H. Lurie Comprehensive Cancer Center of Northwestern UniversityUniversity of Pittsburgh · USUPMC Hillman Cancer Center · USUniversity of California San Diego · US

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Jessie Nedrow · 1988 to 2026
$158.0M
TrainingP41GM103712 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI AYOOB, JOSEPH C · 2012 to 2021
$16.3M
TrainingU54HG008540 · NHGRI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BAHAR, IVET, BERG, JEREMY M · 2014 to 2018
$12.8M
NIDA Center of Excellence OF Computational Drug Abuse Research (CDAR)P30DA035778 · NIDA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BAHAR, IVET, XIE, XIANG-QUN · 2014 to 2018
$5.4M
Interplay between Cdh1/APC and Rad17 in DNA damage checkpoints and carcinogenesisR01CA154695 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WAN, YONG · 2011 to 2015
$1.5M
Interplay between ER and TGF-b in carcinogenesisR01CA202948 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WAN, YONG · 2016 to 2021
$1.4M
NCI NIH HHS P30 CA047904NCI NIH HHS R01 CA154695NCI NIH HHS R01 CA202948NHGRI NIH HHS U54 HG008540NIDA NIH HHS P30 DA035778NIGMS NIH HHS P41 GM103712
6 · The paper itself

Abstract

EIF3H is presumed to be a critical translational initiation factor. Here, our unbiased screening for tumor invasion factors has identified an unexpected role for EIF3H as a deubiquitylating enzyme that dictates breast tumor invasion and metastasis by modulating the Hippo-YAP pathway. EIF3H catalyzed YAP for deubiquitylation, resulting in its stabilization. Structure-based molecular modeling and simulations coupled with biochemical characterization unveiled a unique catalytic mechanism for EIF3H in dissociating polyubiquitin chains from YAP through a catalytic triad consisting of Asp90, Asp91, and Gln121. Trp119 and Tyr 140 on EIF3H directly interacted with the N-terminal region of YAP1, facilitating complex formation of EIF3H and YAP1 for YAP1 deubiquitylation. Stabilization of YAP via elevated EIF3H promoted tumor invasion and metastasis. Interference of EIF3H-mediated YAP deubiquitylation blocked YAP-induced tumor progression and metastasis in breast cancer models. These findings point to a critical role for YAP regulation by EIF3H in tumor invasion and metastasis. SIGNIFICANCE: This work demonstrates that EIF3H is a novel

Indexed as

Adaptor Proteins, Signal TransducingAdultAgedAged, 80 and overAnimalsBiocatalysisBreastBreast NeoplasmsCarcinogenesisCarcinoma, Ductal, BreastCell Line, TumorDeubiquitinating EnzymesDisease-Free SurvivalDisease Models, AnimalEukaryotic Initiation Factor-3FemaleAdaptor Proteins, Signal TransducingDeubiquitinating EnzymesEIF3I protein, humanEukaryotic Initiation Factor-3Protein Serine-Threonine KinasesTranscription FactorsYAP1 protein, humanYAP-Signaling Proteins

Identifiers

PMID32269044
PMCPMC7316131
OpenAlexW3015461923

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.