Evidence map›Paper›PMID 30470740›Full record

ArticleNature communications2018

Autophagy is a gatekeeper of hepatic differentiation and carcinogenesis by controlling the degradation of Yap.

Youngmin A Lee, Luke A Noon, Kemal M Akat, Maria D Ybanez, Ting-Fang Lee, Marie-Luise Berres, Naoto Fujiwara, Nicolas Goossens, Hsin-I Chou, Fatemeh P Parvin-Nejad and 14 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 101 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed, 1 pooled it
7.5field-weighted citation impact, top 2% 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

101 citing papers in PubMed, 1 synthesis or guideline pooled it, 160 citations in OpenAlex.

  1. Pooled it
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  15. Roles of the Keap1/Nrf2 pathway and mitophagy in liver diseases.Journal of Zhejiang University. Science. B · 2025
    Review
  16. Review
  17. Review
  18. SNRK tames mTOR against metabolic dysfunction-associated steatotic liver disease.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
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  20. Article

41 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

24 authors at 10 institutions in 4 countries.

Youngmin A LeeDivision of Liver Diseases, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA. ylee04@rockefeller.edu.
Luke A NoonDivision of Liver Diseases, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Kemal M AkatLaboratory of RNA Molecular Biology, Rockefeller University, New York, NY, 10065, USA.
Maria D YbanezDivision of Liver Diseases, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Ting-Fang LeeDivision of Liver Diseases, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Marie-Luise BerresDepartment of Internal Medicine III, University Hospital RWTH Aachen, 52074, Aachen, Germany.
Naoto FujiwaraDivision of Liver Diseases, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Nicolas GoossensDivision of Liver Diseases, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Hsin-I ChouDivision of Liver Diseases, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Fatemeh P Parvin-NejadDivision of Liver Diseases, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Bilon KhambuDepartment of Pathology & Laboratory Medicine, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Elisabeth G M KramerDepartment of Neurology, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Ronald GordonDepartment for Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Cathie PflegerDepartment of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Doris GermainDepartment of Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Gareth R JohnDepartment of Neurology, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Kirk N CampbellDivision of Nephrology, Icahn School of Medicine at Mount Sinai, NY, 10029, New York, USA.
Zhenyu YueDepartment of Neurology, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Xiao-Ming YinDepartment of Pathology & Laboratory Medicine, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Ana Maria CuervoDepartment of Developmental and Molecular Biology, Institute for Aging Studies, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.ORCID http://orcid.org/0000-0002-0771-700X
Mark J CzajaDepartment of Medicine, Emory University School of Medicine, Atlanta, GA, GA 30307, USA.
M Isabel FielDepartment for Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Yujin HoshidaDivision of Liver Diseases, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.ORCID http://orcid.org/0000-0001-9430-1426
Scott L FriedmanDivision of Liver Diseases, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.ORCID http://orcid.org/0000-0003-1178-6195
Icahn School of Medicine at Mount Sinai · USAllen Institute for Brain Science · USIndiana University School of MedicineRockefeller University · USThe University of Texas Southwestern Medical Center · USAlbert Einstein College of Medicine · USCentro de Investigacion Principe Felipe · ESEmory University · USRWTH Aachen University · DEUniversity Hospital of Geneva · CH

Funding

Developing, Demonstrating, and Disseminating Innovative Programs to Achieve Translational SuccessUL1TR001866 · NCATS · ROCKEFELLER UNIVERSITY · PI COLLER, BARRY, KRUEGER, JAMES G · 2016 to 2025
$40.6M
Role of Autophagy in T Cell Function and Immunosenescence (Project 3)P01AG031782 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI MACIAN, FERNANDO · 2009 to 2024
$36.2M
THE TISCH CANCER INSTITUTE - CANCER CENTER SUPPORT GRANTP30CA196521 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Deanna L Benson · 2015 to 2026
$35.4M
Einstein's Nathan Shock Center of Excellence in Basic Biology of AgingP30AG038072 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI VIJG, JAN · 2010 to 2024
$10.8M
MODULATION OF ACUTE TOXIC LIVER INJURYR01DK044234 · NIDDK · YESHIVA UNIVERSITY · PI SRINIVASAN, SHANTHI K · 1992 to 2023
$7.6M
The Role of KLF6 in Hepatic FibrosisR01DK056621 · NIDDK · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI FRIEDMAN, SCOTT L. · 2000 to 2019
$6.2M
Decreased Protein Degradation in AgingR37AG021904 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI CUERVO, ANA MARIA · 2013 to 2022
$4.4M
Mount Sinai Nephrology Research Training GrantT32DK007757 · NIDDK · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI CAMPBELL, KIRK N, HE, JOHN CIJIANG · 1998 to 2022
$3.8M
Molecular Prognostic Indicators in Liver Cirrhosis and CancerR01DK099558 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HOSHIDA, YUJIN · 2013 to 2016
$2.6M
The role of dendrin in glomerular disease progressionR01DK103022 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CAMPBELL, KIRK N · 2015 to 2019
$1.9M
Autophagy during hepatic stellate cell activation in alcoholic liver injuryR01AA020709 · NIAAA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI FRIEDMAN, SCOTT L. · 2011 to 2015
$1.8M
Rabex-5 regulation of Ras and Notch signaling in development and diseaseR01GM122995 · NIGMS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI PFLEGER, CATHIE M · 2017 to 2020
$1.3M
European Research Council 671231NCATS NIH HHS UL1 TR001866NCI NIH HHS P30 CA196521NIAAA NIH HHS R01 AA020709NIA NIH HHS P30 AG038072NIA NIH HHS R37 AG021904NIDDK NIH HHS R01 DK044234NIDDK NIH HHS R01 DK056621NIDDK NIH HHS R01 DK099558NIDDK NIH HHS R01 DK103022NIDDK NIH HHS R56 DK044234NIDDK NIH HHS T32 DK007757NIGMS NIH HHS R01 GM122995
6 · The paper itself

Abstract

Activation of the Hippo pathway effector Yap underlies many liver cancers, however no germline or somatic mutations have been identified. Autophagy maintains essential metabolic functions of the liver, and autophagy-deficient murine models develop benign adenomas and hepatomegaly, which have been attributed to activation of the p62/Sqstm1-Nrf2 axis. Here, we show that Yap is an autophagy substrate and mediator of tissue remodeling and hepatocarcinogenesis independent of the p62/Sqstm1-Nrf2 axis. Hepatocyte-specific deletion of Atg7 promotes liver size, fibrosis, progenitor cell expansion, and hepatocarcinogenesis, which is rescued by concurrent deletion of Yap. Our results shed new light on mechanisms of Yap degradation and the sequence of events that follow disruption of autophagy, which is impaired in chronic liver disease.

Indexed as

AutophagyAdaptor Proteins, Signal TransducingAnimalsAutophagy-Related Protein 7CarcinogenesisCell Cycle ProteinsCell DifferentiationFemaleHepatocytesHumansLiverLiver NeoplasmsMaleMicePhosphoproteinsProteolysisAdaptor Proteins, Signal TransducingAutophagy-Related Protein 7Cell Cycle ProteinsPhosphoproteinsTranscription FactorsYAP1 protein, humanYap1 protein, mouseYAP-Signaling Proteins

Identifiers

PMID30470740
PMCPMC6251897
OpenAlexW2901619345

What OpenQuestion holds

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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.