• 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

    A cancer-associated, genome protective programme engaging PKC?

    • CSV
    • RefMan
    • EndNote
    • BibTex
    • RefWorks
    Thumbnail
    Name:
    33039823.pdf
    Size:
    1.026Mb
    Format:
    PDF
    Description:
    From UNPAYWALL
    Download
    Authors
    Parker, P. J.
    Lockwood, N.
    Davis, K.
    Kelly, Joanna R
    Soliman, T. N.
    Pardo, A. L.
    Marshall, J. J. T.
    Redmond, J. M.
    Vitale, M.
    Silvia, M.
    Affiliation
    Protein Phosphorylation Laboratory, Francis Crick Institute, London, NW1 1AT, UK; School of Cancer and Pharmaceutical Sciences, Guy's Campus, London, SE1 1UL
    Issue Date
    2020
    
    Metadata
    Show full item record
    Abstract
    Associated with their roles as targets for tumour promoters, there has been a long-standing interest in how members of the protein kinase C (PKC) family act to modulate cell growth and division. This has generated a great deal of observational data, but has for the most part not afforded clear mechanistic insights into the control mechanisms at play. Here, we review the roles of PKC? in protecting transformed cells from non-disjunction. In this particular cell cycle context, there is a growing understanding of the pathways involved, affording biomarker and interventional insights and opportunities.
    Citation
    Parker PJ, Lockwood N, Davis K, Kelly JR, Soliman TN, Pardo AL, et al. A cancer-associated, genome protective programme engaging PKCepsilon. Adv Biol Regul. 2020;78:100759.
    Journal
    Advances in Biological Regulation
    URI
    http://hdl.handle.net/10541/623422
    DOI
    10.1016/j.jbior.2020.100759
    PubMed ID
    33039823
    Additional Links
    https://dx.doi.org/10.1016/j.jbior.2020.100759
    Type
    Article
    Language
    en
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.jbior.2020.100759
    Scopus Count
    Collections
    All Paterson Institute for Cancer Research

    entitlement

    Related articles

    • A genetically-encoded crosslinker screen identifies SERBP1 as a PKCε substrate influencing translation and cell division.
    • Authors: Martini S, Davis K, Faraway R, Elze L, Lockwood N, Jones A, Xie X, McDonald NQ, Mann DJ, Armstrong A, Ule J, Parker PJ
    • Issue date: 2021 Nov 26
    • GH3B6 pituitary tumor cell proliferation is mediated by PKCalpha and PKCepsilon via ERK 1/2-dependent pathway.
    • Authors: Petiti JP, Gutiérrez S, De Paul AL, Andreoli V, Palmeri CM, Sosa Ldel V, Bocco JL, Torres AI
    • Issue date: 2010
    • PKCε inhibits isolation and stemness of side population cells via the suppression of ABCB1 transporter and PI3K/Akt, MAPK/ERK signaling in renal cell carcinoma cell line 769P.
    • Authors: Huang B, Fu SJ, Fan WZ, Wang ZH, Chen ZB, Guo SJ, Chen JX, Qiu SP
    • Issue date: 2016 Jun 28
    • Carbon source-dependent regulation of cell growth by murine protein kinase C epsilon expression in Saccharomyces cerevisiae.
    • Authors: Parissenti AM, Villeneuve D, Kirwan-Rhude A, Busch D
    • Issue date: 1999 Feb
    • Protein kinase Cepsilon makes the life and death decision.
    • Authors: Basu A, Sivaprasad U
    • Issue date: 2007 Aug
    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.