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From Na+/K+-ATPase and Cardiac Glycosides to Cytotoxicity and Cancer Treatment

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00159816%3A_____%2F13%3A00063519" target="_blank" >RIV/00159816:_____/13:00063519 - isvavai.cz</a>

  • Alternative codes found

    RIV/62156489:43210/13:00212729 RIV/00216305:26220/13:PU105353

  • Result on the web

    <a href="http://dx.doi.org/10.2174/18715206113139990304" target="_blank" >http://dx.doi.org/10.2174/18715206113139990304</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.2174/18715206113139990304" target="_blank" >10.2174/18715206113139990304</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    From Na+/K+-ATPase and Cardiac Glycosides to Cytotoxicity and Cancer Treatment

  • Original language description

    The cardiac glycosides are a group of compounds isolated from plants and some animals. They have been used in therapy for heart failure for many years. The cytotoxic effect of many cardiac glycosides has been demonstrated, but the mechanism of action isvery complicated and complex, and Na+/K+-ATPase surely plays a crucial role in it. On the other hand, Na+/K+-ATPase is regulated by many endogenous factors, such as hormones or FXYD proteins, whose role in regulating the cell cycle has been studied intensively. This review focuses on the role of Na+/K+-ATPase in regulating the cell growth, the cell cycle and the cell proliferation and on the involvement of cardiac glycosides in regulating Na+/K+-ATPase. The cytotoxic effect of cardiac glycosides is discussed with respect to the apoptotic mechanisms possibly induced by these compounds. Novel strategies in cancer therapy based on cardiac glycosides are discussed as are possibilities for counteracting multidrug resistance by using cardiac

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FD - Oncology and haematology

  • OECD FORD branch

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2013

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Anti-Cancer Agents in Medicinal Chemistry

  • ISSN

    1871-5206

  • e-ISSN

  • Volume of the periodical

    13

  • Issue of the periodical within the volume

    7

  • Country of publishing house

    AE - UNITED ARAB EMIRATES

  • Number of pages

    19

  • Pages from-to

    1069-1087

  • UT code for WoS article

    000324249500013

  • EID of the result in the Scopus database