• Login
    View Item 
    •   Home
    • The Manchester Institute Cancer Research UK
    • All Paterson Institute for Cancer Research
    • View Item
    •   Home
    • The Manchester Institute Cancer Research UK
    • All Paterson Institute for Cancer Research
    • View Item
    JavaScript is disabled for your browser. Some features of this site may not work without it.

    Browse

    All of ChristieCommunitiesTitleAuthorsIssue DateSubmit DateSubjectsThis CollectionTitleAuthorsIssue DateSubmit DateSubjectsProfilesView

    My Account

    LoginRegister

    Local Links

    The Christie WebsiteChristie Library and Knowledge Service

    Statistics

    Display statistics

    TIAM1 antagonizes TAZ/YAP both in the destruction complex in the cytoplasm and in the nucleus to inhibit invasion of intestinal epithelial cells.

    • CSV
    • RefMan
    • EndNote
    • BibTex
    • RefWorks
    Authors
    Diamantopoulou, Zoi
    White, Gavin R M
    Fadlullah, Muhammad Z H
    Dreger, M
    Pickering, K
    Maltas, J
    Ashton, Garry
    MacLeod, R
    Baillie, G
    Kouskoff, Valerie
    Lacaud, Georges
    Murray, G
    Sansom, O
    Hurlstone, A
    Malliri, Angeliki
    Show allShow less
    Affiliation
    Cell Signalling Group, Cancer Research UK Manchester Institute, The University of Manchester, Manchester M20 4BX
    Issue Date
    2017-05-08
    
    Metadata
    Show full item record
    Abstract
    Aberrant WNT signaling drives colorectal cancer (CRC). Here, we identify TIAM1 as a critical antagonist of CRC progression through inhibiting TAZ and YAP, effectors of WNT signaling. We demonstrate that TIAM1 shuttles between the cytoplasm and nucleus antagonizing TAZ/YAP by distinct mechanisms in the two compartments. In the cytoplasm, TIAM1 localizes to the destruction complex and promotes TAZ degradation by enhancing its interaction with βTrCP. Nuclear TIAM1 suppresses TAZ/YAP interaction with TEADs, inhibiting expression of TAZ/YAP target genes implicated in epithelial-mesenchymal transition, cell migration, and invasion, and consequently suppresses CRC cell migration and invasion. Importantly, high nuclear TIAM1 in clinical specimens associates with increased CRC patient survival. Together, our findings suggest that in CRC TIAM1 suppresses tumor progression by regulating YAP/TAZ activity.
    Citation
    TIAM1 antagonizes TAZ/YAP both in the destruction complex in the cytoplasm and in the nucleus to inhibit invasion of intestinal epithelial cells. 2017, 31 (5):621-634.e6 Cancer Cell
    Journal
    Cancer Cell
    URI
    http://hdl.handle.net/10541/620353
    DOI
    10.1016/j.ccell.2017.03.007
    PubMed ID
    28416184
    Type
    Article
    Language
    en
    ISSN
    1878-3686
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.ccell.2017.03.007
    Scopus Count
    Collections
    All Paterson Institute for Cancer Research

    entitlement

    Related articles

    • Actin like-6A promotes glioma progression through stabilization of transcriptional regulators YAP/TAZ.
    • Authors: Ji J, Xu R, Zhang X, Han M, Xu Y, Wei Y, Ding K, Wang S, Bin Huang, Chen A, Di Zhang, Jiang Z, Xu S, Zhang Q, Li W, Ni S, Wang J, Li X
    • Issue date: 2018 May 1
    • TAZ Protein Accumulation Is Negatively Regulated by YAP Abundance in Mammalian Cells.
    • Authors: Finch-Edmondson ML, Strauss RP, Passman AM, Sudol M, Yeoh GC, Callus BA
    • Issue date: 2015 Nov 13
    • HERC3 promotes YAP/TAZ stability and tumorigenesis independently of its ubiquitin ligase activity.
    • Authors: Yuan B, Liu J, Shi A, Cao J, Yu Y, Zhu Y, Zhang C, Qiu Y, Luo H, Shi J, Cao X, Xu P, Shen L, Liang T, Zhao B, Feng XH
    • Issue date: 2023 Feb 15
    • Nuclear phosphoinositide signaling promotes YAP/TAZ-TEAD transcriptional activity in breast cancer.
    • Authors: Jung O, Baek MJ, Wooldrik C, Johnson KR, Fisher KW, Lou J, Ricks TJ, Wen T, Best MD, Cryns VL, Anderson RA, Choi S
    • Issue date: 2024 May
    • A MYC-Driven Change in Mitochondrial Dynamics Limits YAP/TAZ Function in Mammary Epithelial Cells and Breast Cancer.
    • Authors: von Eyss B, Jaenicke LA, Kortlever RM, Royla N, Wiese KE, Letschert S, McDuffus LA, Sauer M, Rosenwald A, Evan GI, Kempa S, Eilers M
    • Issue date: 2015 Dec 14
    DSpace software (copyright © 2002 - 2025)  DuraSpace
    Quick Guide | Contact Us
    Open Repository is a service operated by 
    Atmire NV
     

    Export search results

    The export option will allow you to export the current search results of the entered query to a file. Different formats are available for download. To export the items, click on the button corresponding with the preferred download format.

    By default, clicking on the export buttons will result in a download of the allowed maximum amount of items.

    To select a subset of the search results, click "Selective Export" button and make a selection of the items you want to export. The amount of items that can be exported at once is similarly restricted as the full export.

    After making a selection, click one of the export format buttons. The amount of items that will be exported is indicated in the bubble next to export format.