Evidence map›Paper›PMID 31000600›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Hippo signaling is intrinsically regulated during cell cycle progression by APC/C

Wantae Kim, Yong Suk Cho, Xiaohui Wang, Ogyi Park, Xueyan Ma, Hanjun Kim, Wenjian Gan, Eek-Hoon Jho, Boksik Cha, Yun-Ji Jeung and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

46 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
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  4. Frontiers in cell and developmental biology · 2026
    Review
  5. Targeting ubiquitination in disease and therapy.Signal transduction and targeted therapy · 2025
    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

16 authors at 9 institutions in 3 countries.

Wantae KimDepartment of Developmental Biology, Harvard Stem Cell Institute, Harvard School of Dental Medicine, Boston, MA 02215.
Yong Suk ChoDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Xiaohui WangDepartment of Developmental Biology, Harvard Stem Cell Institute, Harvard School of Dental Medicine, Boston, MA 02215.
Ogyi ParkSection on Liver Biology, National Institute on Alcohol Abuse and Alcoholism, National Institute of Health, Bethesda, MD 20892.
Xueyan MaShanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, 200031 Shanghai, China.
Hanjun KimDepartment of Developmental Biology, Harvard Stem Cell Institute, Harvard School of Dental Medicine, Boston, MA 02215.ORCID 0000-0001-9364-462X
Wenjian GanDepartment of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215.
Eek-Hoon JhoDepartment of Life Science, University of Seoul, 02504 Seoul, South Korea.
Boksik ChaCardiovascular Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK 73104.
Yun-Ji JeungBiomedical Translational Research Center, Korea Research Institute of Bioscience and Biotechnology, 34141 Daejeon, Republic of Korea.
Lei ZhangShanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, 200031 Shanghai, China.
Bin GaoSection on Liver Biology, National Institute on Alcohol Abuse and Alcoholism, National Institute of Health, Bethesda, MD 20892.
Wenyi WeiDepartment of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215.
Jin JiangDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Kyung-Sook ChungBiomedical Translational Research Center, Korea Research Institute of Bioscience and Biotechnology, 34141 Daejeon, Republic of Korea; kschung@kribb.re.kr yingzi_yang@hsdm.harvard.edu.ORCID 0000-0002-0862-0779
Yingzi YangDepartment of Developmental Biology, Harvard Stem Cell Institute, Harvard School of Dental Medicine, Boston, MA 02215; kschung@kribb.re.kr yingzi_yang@hsdm.harvard.edu.ORCID 0000-0003-3933-887X
Harvard Stem Cell Institute · USBeth Israel Deaconess Medical Center · USChinese Academy of Sciences · CNKorea Research Institute of Bioscience and Biotechnology · KRNational Institute on Alcohol Abuse and Alcoholism · USThe University of Texas Southwestern Medical Center · USChungnam National University · KROklahoma Medical Research Foundation · USUniversity of Seoul · KR

Funding

HARVARD CLINICAL AND TRANSLATIONAL SCIENCE CENTER (UL1)UL1RR025758 · NCRR · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2008 to 2011
$91.4M
Molecular mechanisms of liver injury, repair, and immunityZIAAA000368 · NIAAA · NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM · PI GAO, BIN · 2009 to 2023
$16.1M
Cell signaling in development and regenerationR35GM118063 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI Jin Jiang · 2016 to 2026
$9.4M
Interplay between Cdh1 and major regulatory pathways in human cancerR01GM089763 · NIGMS · BETH ISRAEL DEACONESS MEDICAL CENTER · PI WEI, WENYI · 2009 to 2018
$3.0M
Cellular and molecular mechanism of Hippo signaling in suppressing liver tumor formationR01CA222571 · NCI · HARVARD MEDICAL SCHOOL · PI YANG, YINGZI · 2018 to 2022
$1.9M
Mechanisms of Hippo signaling in Alcoholic liver diseaseR21AA025725 · NIAAA · HARVARD MEDICAL SCHOOL · PI YANG, YINGZI · 2017 to 2018
$445k
NCI NIH HHS R01 CA222571NCRR NIH HHS UL1 RR025758NIAAA NIH HHS R21 AA025725NIGMS NIH HHS R01 GM089763NIGMS NIH HHS R35 GM118063
6 · The paper itself

Abstract

The Hippo-YAP/TAZ signaling pathway plays a pivotal role in growth control during development and regeneration and its dysregulation is widely implicated in various cancers. To further understand the cellular and molecular mechanisms underlying Hippo signaling regulation, we have found that activities of core Hippo signaling components, large tumor suppressor (LATS) kinases and YAP/TAZ transcription factors, oscillate during mitotic cell cycle. We further identified that the anaphase-promoting complex/cyclosome (APC/C)

Indexed as

Anaphase-Promoting Complex-CyclosomeAnimalsAntigens, CDCadherinsCdh1 ProteinsDrosophila melanogasterDrosophila ProteinsG1 PhaseHEK293 CellsHeLa CellsHippo KinasesHippo Signaling PathwayHumansIntracellular Signaling Peptides and ProteinsProtein KinasesProtein Serine-Threonine KinasesAnaphase-Promoting Complex-CyclosomeAntigens, CDCadherinsCDH1 protein, humanCdh1 ProteinsDrosophila Proteinsfzr protein, DrosophilaHippo Kinaseshpo protein, DrosophilaIntracellular Signaling Peptides and ProteinsLATS1 protein, humanProtein KinasesProtein Serine-Threonine Kinaseswts protein, DrosophilaAPC/CCdh1Hippo signalingLATS1/2mitotic cell cycleYAP/TAZ

Identifiers

PMID31000600
PMCPMC6511010
OpenAlexW2940319923

What Socratic holds

Textmetadata
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.