Making Connections: p53 and the Cathepsin Proteases as Co-Regulators of Cancer and Apoptosis

• Published in: Cancers Vol. 12; no. 11; p. 3476
• Main Authors: Soond, Surinder M., Savvateeva, Lyudmila V., Makarov, Vladimir A., Gorokhovets, Neonila V., Townsend, Paul A., Zamyatnin, Andrey A.
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 22-11-2020; MDPI
• Subjects: Apoptosis; Cancer; Cathepsins; Cell cycle; Cell death; Cellular stress response; Cytoplasm; Cytotoxicity; Deoxyribonucleic acid; DNA; DNA damage; DNA repair; Extracellular matrix; Gene expression; Gene regulation; Genomes; Health aspects; Homeostasis; Intermediates; Isoforms; Kinases; Mutation; p53 Protein; Phosphorylation; Physiological aspects; Proteases; Proteins; Review; Signal transduction; Transcription; Tumor suppressor genes; Russia
• ISSN: 2072-6694; 2072-6694
• DOI: 10.3390/cancers12113476

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.