Evidence map›Paper›PMID 28866620›Full record

ArticleGut2018

Hepatic Hippo signaling inhibits protumoural microenvironment to suppress hepatocellular carcinoma.

Wantae Kim, Sanjoy Kumar Khan, Yuchen Liu, Ruoshi Xu, Ogyi Park, Yong He, Boksik Cha, Bin Gao, Yingzi Yang

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Gut, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed
7.1field-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

93 citing papers in PubMed, 162 citations in OpenAlex.

  1. Article
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  7. MST1/2 DKO abates salvianolic acid B's therapeutic effect on CClNaunyn-Schmiedeberg's archives of pharmacology · 2025
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  11. Review
  12. Hepatocellular carcinoma: signaling pathways and therapeutic advances.Signal transduction and targeted therapy · 2025
    Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. Review

33 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

9 authors at 4 institutions in 2 countries.

Wantae Kim *Department of Developmental Biology, Harvard School of Dental Medicine, Boston, Massachusetts, USA.
Sanjoy Kumar Khan *Department of Developmental Biology, Harvard School of Dental Medicine, Boston, Massachusetts, USA.
Yuchen Liu *Department of Developmental Biology, Harvard School of Dental Medicine, Boston, Massachusetts, USA.
Ruoshi XuDepartment of Developmental Biology, Harvard School of Dental Medicine, Boston, Massachusetts, USA.
Ogyi ParkLaboratory of Liver Diseases, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, Maryland, USA.
Yong HeLaboratory of Liver Diseases, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, Maryland, USA.
Boksik ChaCardiovascular Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma, USA.
Bin GaoLaboratory of Liver Diseases, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, Maryland, USA.
Yingzi YangDepartment of Developmental Biology, Harvard School of Dental Medicine, Boston, Massachusetts, USA.
Harvard University · USNational Institute on Alcohol Abuse and Alcoholism · USNational Institutes of Health · USOklahoma Medical Research Foundation · US

Funding

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 CA222571
6 · The paper itself

Abstract

objectiveHippo signalling is a recently identified major oncosuppressive pathway that plays critical roles in inhibiting hepatocyte proliferation, survival and hepatocellular carcinoma (HCC) formation. Hippo kinase (Mst1 and Mst2) inhibits HCC proliferation by suppressing Yap/Taz transcription activities. As human HCC is mainly driven by chronic liver inflammation, it is not clear whether Hippo signalling inhibits HCC by shaping its inflammatory microenvironment.

designWe have established a genetic HCC model by deleting

resultsGenetic deletion of Mst1 and Mst2 in hepatocytes (DKO) led to HCC development, highly upregulated

conclusionsHippo signalling in hepatocytes maintains normal liver growth by suppressing macrophage infiltration during protumoural microenvironment formation through the inhibition of Yap-dependent

Indexed as

Signal TransductionAnimalsCarcinoma, HepatocellularCell ProliferationCell Transformation, NeoplasticHepatocyte Growth FactorHepatocytesHippo KinasesHippo Signaling PathwayLiver Neoplasms, ExperimentalMiceMice, Mutant StrainsPhosphoproteinsProtein Serine-Threonine KinasesProto-Oncogene ProteinsSerine-Threonine Kinase 3Hepatocyte Growth FactorHippo Kinasesmacrophage stimulating proteinPhosphoproteinsProtein Serine-Threonine KinasesProto-Oncogene ProteinsSerine-Threonine Kinase 3Stk3 protein, mouseTranscription FactorsCancerHepatocellular CarcinomaInflammationLiverMacrophages

Identifiers

PMID28866620
PMCPMC6592016
OpenAlexW2753263260

What OpenQuestion holds

Textmetadata
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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 OpenQuestion graph.