Evidence map›Paper›PMID 28947795›Full record

ArticleNature communications2017

Stable MOB1 interaction with Hippo/MST is not essential for development and tissue growth control.

Yavuz Kulaberoglu, Kui Lin, Maxine Holder, Zhongchao Gai, Marta Gomez, Belul Assefa Shifa, Merdiye Mavis, Lily Hoa, Ahmad A D Sharif, Celia Lujan and 5 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. The Hippo Pathway in Breast Cancer: The Extracellular Matrix and Hypoxia.International journal of molecular sciences · 2024
    Review
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  14. TheProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
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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

15 authors at 5 institutions in 2 countries.

Yavuz KulaberogluTumour Suppressor Signalling Network Laboratory, UCL Cancer Institute, University College London, London, WC1E 6BT, UK.ORCID http://orcid.org/0000-0003-2372-184X
Kui LinState Key Laboratory of Microbial Metabolism, School of Life Sciences & Biotechnology, Shanghai Jiao Tong University, Shanghai, 200240, China.
Maxine HolderApoptosis and Proliferation Control Laboratory, Francis Crick Institute, London, NW1 1BF, UK.
Zhongchao GaiState Key Laboratory of Microbial Metabolism, School of Life Sciences & Biotechnology, Shanghai Jiao Tong University, Shanghai, 200240, China.
Marta GomezTumour Suppressor Signalling Network Laboratory, UCL Cancer Institute, University College London, London, WC1E 6BT, UK.
Belul Assefa ShifaTumour Suppressor Signalling Network Laboratory, UCL Cancer Institute, University College London, London, WC1E 6BT, UK.
Merdiye MavisTumour Suppressor Signalling Network Laboratory, UCL Cancer Institute, University College London, London, WC1E 6BT, UK.
Lily HoaTumour Suppressor Signalling Network Laboratory, UCL Cancer Institute, University College London, London, WC1E 6BT, UK.
Ahmad A D SharifTumour Suppressor Signalling Network Laboratory, UCL Cancer Institute, University College London, London, WC1E 6BT, UK.
Celia LujanMolecular Biology of Cancer laboratory, UCL Cancer Institute, University College London, London, WC1E 6BT, UK.
Ewan St John SmithDepartment of Pharmacology, University of Cambridge, Cambridge, CB2 1PD, UK.ORCID http://orcid.org/0000-0002-2699-1979
Ivana BjedovMolecular Biology of Cancer laboratory, UCL Cancer Institute, University College London, London, WC1E 6BT, UK.
Nicolas TaponApoptosis and Proliferation Control Laboratory, Francis Crick Institute, London, NW1 1BF, UK.
Geng WuState Key Laboratory of Microbial Metabolism, School of Life Sciences & Biotechnology, Shanghai Jiao Tong University, Shanghai, 200240, China. geng.wu@sjtu.edu.cn.
Alexander HergovichTumour Suppressor Signalling Network Laboratory, UCL Cancer Institute, University College London, London, WC1E 6BT, UK. a.hergovich@ucl.ac.uk.
University College London · GBShanghai Jiao Tong University · CNThe Francis Crick Institute · GBUniversity of Cambridge · GBCancer Research UK · GB

Funding

DROSOPHILA GENOMICS RESOURCE CENTERP40OD010949 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Andrew Zelhof · 2012 to 2026
$9.4M
Cancer Research UK 17064European Research CouncilNIH HHS P40 OD010949Wellcome Trust FC001175
6 · The paper itself

Abstract

The Hippo tumor suppressor pathway is essential for development and tissue growth control, encompassing a core cassette consisting of the Hippo (MST1/2), Warts (LATS1/2), and Tricornered (NDR1/2) kinases together with MOB1 as an important signaling adaptor. However, it remains unclear which regulatory interactions between MOB1 and the different Hippo core kinases coordinate development, tissue growth, and tumor suppression. Here, we report the crystal structure of the MOB1/NDR2 complex and define key MOB1 residues mediating MOB1's differential binding to Hippo core kinases, thereby establishing MOB1 variants with selective loss-of-interaction. By studying these variants in human cancer cells and Drosophila, we uncovered that MOB1/Warts binding is essential for tumor suppression, tissue growth control, and development, while stable MOB1/Hippo binding is dispensable and MOB1/Trc binding alone is insufficient. Collectively, we decrypt molecularly, cell biologically, and genetically the importance of the diverse interactions of Hippo core kinases with the pivotal MOB1 signal transducer.The Hippo tumor suppressor pathway is essential for development and tissue growth control. Here the authors employ a multi-disciplinary approach to characterize the interactions of the three Hippo kinases with the signaling adaptor MOB1 and show how they differently affect development, tissue growth and tumor suppression.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsAnimals, Genetically ModifiedCell LineCell Line, TumorDrosophila melanogasterHippo Signaling PathwayHumansMAP Kinase Kinase KinasesModels, MolecularProtein ConformationProtein Serine-Threonine KinasesTumor Suppressor ProteinsAdaptor Proteins, Signal TransducingLATS1 protein, humanLATS2 protein, humanMAP3K10 protein, humanMAP Kinase Kinase KinasesMOB1A protein, humanProtein Serine-Threonine KinasesSTK38L protein, humanTumor Suppressor Proteins

Identifiers

PMID28947795
PMCPMC5612953
OpenAlexW2755900985

What OpenQuestion holds

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Registered trials

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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.