Evidence map›Paper›PMID 24362629›Full record

ArticleNature cell biology2014

A genetic screen identifies an LKB1-MARK signalling axis controlling the Hippo-YAP pathway.

Morvarid Mohseni, Jianlong Sun, Allison Lau, Stephen Curtis, Jeffrey Goldsmith, Victor L Fox, Chongjuan Wei, Marsha Frazier, Owen Samson, Kwok-Kin Wong and 3 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Nature cell biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 184 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
184citing papers in PubMed, 2 pooled it
14.3field-weighted citation impact, top 1% 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

184 citing papers in PubMed, 2 syntheses or guidelines pooled it, 293 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  7. medRxiv : the preprint server for health sciences · 2026
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  17. Stearoylation cycle regulates the cell surface distribution of the PCP protein Vangl2.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  18. Article
  19. LKB1 biology: assessing the therapeutic relevancy of LKB1 inhibitors.Cell communication and signaling : CCS · 2024
    Review
  20. Review

124 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
    Wong, Kwok-Kim [corrected to Wong, Kwok-Kin]
5 · Who and what money

Authors and funding

13 authors at 5 institutions in 2 countries.

Morvarid Mohseni1] Stem Cell Program, Boston Children's Hospital, Boston, Massachusetts 02115, USA [2] Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, Massachusetts 02138, USA [3] Harvard Stem Cell Institute, Cambridge, Massachusetts 02138, USA.
Jianlong Sun1] Stem Cell Program, Boston Children's Hospital, Boston, Massachusetts 02115, USA [2] Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, Massachusetts 02138, USA [3] Harvard Stem Cell Institute, Cambridge, Massachusetts 02138, USA.
Allison Lau1] Stem Cell Program, Boston Children's Hospital, Boston, Massachusetts 02115, USA [2] Harvard Stem Cell Institute, Cambridge, Massachusetts 02138, USA.
Stephen Curtis1] Stem Cell Program, Boston Children's Hospital, Boston, Massachusetts 02115, USA [2] Harvard Stem Cell Institute, Cambridge, Massachusetts 02138, USA [3] Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115, USA.
Jeffrey GoldsmithCenter for Pediatric Polyposis, Boston Children's Hospital, Boston, Massachusetts 02115, USA.
Victor L FoxDivision of Gastroenterology and Nutrition, Boston Children's Hospital, Boston, Massachusetts 02115, USA.
Chongjuan WeiDepartment of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA.
Marsha FrazierDepartment of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA.
Owen SamsonWnt Signaling and Colorectal Cancer Group, The Beatson Institute for Cancer Research, Cancer Research UK, Glasgow G61 1BD, UK.
Kwok-Kin Wong
Kwok-Kim Wong1] Genetics Division, Department of Medicine Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA [2] Ludwig Center at Dana-Farber/Harvard Cancer Center, Boston, Massachusetts 02115, USA.
Carla Kim1] Stem Cell Program, Boston Children's Hospital, Boston, Massachusetts 02115, USA [2] Harvard Stem Cell Institute, Cambridge, Massachusetts 02138, USA [3] Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115, USA.
Fernando D Camargo1] Stem Cell Program, Boston Children's Hospital, Boston, Massachusetts 02115, USA [2] Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, Massachusetts 02138, USA [3] Harvard Stem Cell Institute, Cambridge, Massachusetts 02138, USA.
Boston Children's Hospital · USHarvard Stem Cell Institute · USThe University of Texas MD Anderson Cancer Center · USCancer Research UK Scotland Institute · GBHarvard University · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Kathrin Milbury · 1985 to 2026
$290.8M
Hippo signaling and the control of epidermal development and growthR01AR064036 · NIAMS · BOSTON CHILDREN'S HOSPITAL · PI CAMARGO, FERNANDO · 2012 to 2016
$1.9M
Reprogramming of liver cell fate by Hippo signalingR01DK099559 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI CAMARGO, FERNANDO · 2013 to 2017
$1.9M
The role of the Hippo pathway on mammalian organ size, progenitor cells and canceR01CA131426 · NCI · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI BRUMMELKAMP, THIJN · 2009 to 2013
$1.4M
NCI NIH HHS R01 CA131426NIAMS NIH HHS R01 AR064036NIDDK NIH HHS R01 DK099559
6 · The paper itself

Abstract

The Hippo-YAP pathway is an emerging signalling cascade involved in the regulation of stem cell activity and organ size. To identify components of this pathway, we performed an RNAi-based kinome screen in human cells. Our screen identified several kinases not previously associated with Hippo signalling that control multiple cellular processes. One of the hits, LKB1, is a common tumour suppressor whose mechanism of action is only partially understood. We demonstrate that LKB1 acts through its substrates of the microtubule affinity-regulating kinase family to regulate the localization of the polarity determinant Scribble and the activity of the core Hippo kinases. Our data also indicate that YAP is functionally important for the tumour suppressive effects of LKB1. Our results identify a signalling axis that links YAP activation with LKB1 mutations, and have implications for the treatment of LKB1-mutant human malignancies. In addition, our findings provide insight into upstream signals of the Hippo-YAP signalling cascade.

Indexed as

Genetic TestingSignal TransductionAdaptor Proteins, Signal TransducingAMP-Activated Protein Kinase KinasesAMP-Activated Protein KinasesAnimalsCell Line, TumorEnzyme ActivationGene Knockdown TechniquesGenes, ReporterHEK293 CellsHippo Signaling PathwayHumansMiceMutationNeoplasmsAdaptor Proteins, Signal TransducingAMP-Activated Protein Kinase KinasesAMP-Activated Protein KinasesMARK1 protein, humanPhosphoproteinsProtein Serine-Threonine KinasesSTK11 protein, humanStk11 protein, mouseTranscription FactorsYAP1 protein, humanYAP-Signaling Proteins

Identifiers

PMID24362629
PMCPMC4159053
OpenAlexW1976323469

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.