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Mitochondria-targeted compounds in the treatment of cancer

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11120%2F20%3A43919920" target="_blank" >RIV/00216208:11120/20:43919920 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.4149/neo_2020_190725N671" target="_blank" >https://doi.org/10.4149/neo_2020_190725N671</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.4149/neo_2020_190725N671" target="_blank" >10.4149/neo_2020_190725N671</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Mitochondria-targeted compounds in the treatment of cancer

  • Original language description

    Mitochondria are highly dynamic organelles involved in many cellular functions. Beyond their central role in metabolism, they also take a part in maintaining calcium homeostasis, cell death, immunity and ROS production. Changes in these functions have been shown to be crucial for the adaptation and survival of cancer cells. Mitochondria therefore constitute a promising target for the development of novel anticancer agents. The triphenylphosphonium (TPP+) moiety has been widely used to target molecules into mitochondria. TPP+ derivatives of a variety of conventional cytostatic drugs, natural substances, metformin, antioxidants or a range of newly synthesized molecules have shown promising results against cancer cells. In this review we discuss biochemical differences between cancer cells and normal cells with specific focus on mitochondria, and how mitochondrially targeted molecules can be used to selectively affect mitochondrial function in normal and cancer cells. We summarize the published data on mitochondrially targeted anticancer agents and propose future research avenues.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10608 - Biochemistry and molecular biology

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2020

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Neoplasma

  • ISSN

    0028-2685

  • e-ISSN

  • Volume of the periodical

    67

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    SK - SLOVAKIA

  • Number of pages

    11

  • Pages from-to

    450-460

  • UT code for WoS article

    000542668500002

  • EID of the result in the Scopus database

    2-s2.0-85084916388