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Mitocans Revisited: Mitochondrial Targeting as Efficient Anti-Cancer Therapy

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    SYSNO ASEP0535784
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleMitocans Revisited: Mitochondrial Targeting as Efficient Anti-Cancer Therapy
    Author(s) Dong, L. (AU)
    Gopalan, V. (US)
    Holland, O. (AU)
    Neužil, Jiří (BTO-N) RID
    Number of authors4
    Article number7941
    Source TitleInternational Journal of Molecular Sciences. - : MDPI
    Roč. 21, č. 21 (2020)
    Number of pages21 s.
    Languageeng - English
    CountryCH - Switzerland
    Keywordsalpha-tocopheryl succinate ; overcoming drug-resistance ; cervical-cancer cells ; glutamine-metabolism ; mitochondrial targeting
    Subject RIVEB - Genetics ; Molecular Biology
    OECD categoryBiochemistry and molecular biology
    Method of publishingOpen access
    Institutional supportBTO-N - RVO:86652036
    UT WOS000589143400001
    EID SCOPUS85094117459
    DOI10.3390/ijms21217941
    AnnotationMitochondria are essential cellular organelles, controlling multiple signalling pathways critical for cell survival and cell death. Increasing evidence suggests that mitochondrial metabolism and functions are indispensable in tumorigenesis and cancer progression, rendering mitochondria and mitochondrial functions as plausible targets for anti-cancer therapeutics. In this review, we summarised the major strategies of selective targeting of mitochondria and their functions to combat cancer, including targeting mitochondrial metabolism, the electron transport chain and tricarboxylic acid cycle, mitochondrial redox signalling pathways, and ROS homeostasis. We highlight that delivering anti-cancer drugs into mitochondria exhibits enormous potential for future cancer therapeutic strategies, with a great advantage of potentially overcoming drug resistance. Mitocans, exemplified by mitochondrially targeted vitamin E succinate and tamoxifen (MitoTam), selectively target cancer cell mitochondria and efficiently kill multiple types of cancer cells by disrupting mitochondrial function, with MitoTam currently undergoing a clinical trial.
    WorkplaceInstitute of Biotechnology
    ContactMonika Kopřivová, Monika.Koprivova@ibt.cas.cz, Tel.: 325 873 700
    Year of Publishing2021
    Electronic addresshttps://www.mdpi.com/1422-0067/21/21/7941
Number of the records: 1  

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