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    Making connections: p53 and the cathepsin proteases as co-regulators of cancer and apoptosis

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    Authors
    Soond, S. M.
    Savvateeva, L. V.
    Makarov, V. A.
    Gorokhovets, N. V.
    Townsend, Paul A
    Zamyatnin, A. A., Jr.
    Affiliation
    Institute of Molecular Medicine, Sechenov First Moscow State Medical University, Trubetskaya Str. 8-2, 119991 Moscow, Russia.
    Issue Date
    2020
    
    Metadata
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    Abstract
    While viewed as the "guardian of the genome", the importance of the tumor suppressor p53 protein has increasingly gained ever more recognition in modulating additional modes of action related to cell death. Slowly but surely, its importance has evolved from a mutated genetic locus heavily implicated in a wide array of cancer types to modulating lysosomal-mediated cell death either directly or indirectly through the transcriptional regulation of the key signal transduction pathway intermediates involved in this. As an important step in determining the fate of cells in response to cytotoxicity or during stress response, lysosomal-mediated cell death has also become strongly interwoven with the key components that give the lysosome functionality in the form of the cathepsin proteases. While a number of articles have been published highlighting the independent input of p53 or cathepsins to cellular homeostasis and disease progression, one key area that warrants further focus is the regulatory relationship that p53 and its isoforms share with such proteases in regulating lysosomal-mediated cell death. Herein, we review recent developments that have shaped this relationship and highlight key areas that need further exploration to aid novel therapeutic design and intervention strategies.
    Citation
    Soond SM, Savvateeva LV, Makarov VA, Gorokhovets NV, Townsend PA, Zamyatnin AA, Jr. Making Connections: p53 and the Cathepsin Proteases as Co-Regulators of Cancer and Apoptosis. Cancers (Basel). 2020;12(11).
    Journal
    Cancers
    URI
    http://hdl.handle.net/10541/623675
    DOI
    10.3390/cancers12113476
    PubMed ID
    33266503
    Additional Links
    https://dx.doi.org/10.3390/cancers12113476
    Type
    Article
    Language
    en
    ae974a485f413a2113503eed53cd6c53
    10.3390/cancers12113476
    Scopus Count
    Collections
    All Paterson Institute for Cancer Research

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