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Inhibitors of Succinate: Quinone Reductase/Complex II Regulate Production of Mitochondrial Reactive Oxygen Species and Protect Normal Cells from Ischemic Damage but Induce Specific Cancer Cell Death

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F86652036%3A_____%2F11%3A00369494" target="_blank" >RIV/86652036:_____/11:00369494 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1007/s11095-011-0566-7" target="_blank" >http://dx.doi.org/10.1007/s11095-011-0566-7</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s11095-011-0566-7" target="_blank" >10.1007/s11095-011-0566-7</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Inhibitors of Succinate: Quinone Reductase/Complex II Regulate Production of Mitochondrial Reactive Oxygen Species and Protect Normal Cells from Ischemic Damage but Induce Specific Cancer Cell Death

  • Original language description

    Succinate:quinone reductase (SQR) of Complex II, occupying a unique central point in the mitochondrial respiratory system as a major source of electrons driving reactive oxygen species (ROS) production, is an ideal pharmaceutical target for modulating ROS levels in normal cells to prevent oxidative stress-induced damage or increase ROS in cancer cells, inducing cell death. Value of drugs like diazoxide to prevent ROS production, protecting normal cells, while vitamin E analogues promote ROS in cancer cells to kill them, is highlighted. We collate and discuss diverse sources of information relating to ROS production in different biological systems, focussing on evidence for SQR as main source of ROS production in mitochondria, particularly its relevanceto protection from oxidative stress and to mitochondrial-targeted anticancer drugs (mitocans) as novel cancer therapies.

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    CE - Biochemistry

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2011

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Pharmaceutical Research

  • ISSN

    0724-8741

  • e-ISSN

  • Volume of the periodical

    28

  • Issue of the periodical within the volume

    11

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    35

  • Pages from-to

    2695-2730

  • UT code for WoS article

    000295697700006

  • EID of the result in the Scopus database