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Importance of ABCC1 for cancer therapy and prognosis

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11140%2F14%3A10281236" target="_blank" >RIV/00216208:11140/14:10281236 - isvavai.cz</a>

  • Alternative codes found

    RIV/75010330:_____/14:00010632 RIV/00216208:11120/14:43909221

  • Result on the web

    <a href="http://dx.doi.org/10.3109/03602532.2014.901348" target="_blank" >http://dx.doi.org/10.3109/03602532.2014.901348</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3109/03602532.2014.901348" target="_blank" >10.3109/03602532.2014.901348</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Importance of ABCC1 for cancer therapy and prognosis

  • Original language description

    Multidrug resistance presents one of the most important causes of cancer treatment failure. Numerous in vitro and in vivo data have made it clear that multidrug resistance is frequently caused by enhanced expression of ATP-binding cassette (ABC) transporters. ABC transporters are membrane-bound proteins involved in cellular defense mechanisms, namely, in outward transport of xenobiotics and physiological substrates. Their function thus prevents toxicity as carcinogenesis on one hand but may contribute to the resistance of tumor cells to a number of drugs including chemotherapeutics on the other. Within 48 members of the human ABC superfamily there are several multidrug resistance-associated transporters. Due to the well documented susceptibility of numerous drugs to efflux via ABC transporters it is highly desirable to assess the status of ABC transporters for individualization of treatment by their substrates. The multidrug resistance associated protein 1 (MRP1) encoded by ABCC1 gene

  • 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

    2014

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Drug Metabolism Reviews

  • ISSN

    0360-2532

  • e-ISSN

  • Volume of the periodical

    46

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    18

  • Pages from-to

    325-342

  • UT code for WoS article

    000340454100005

  • EID of the result in the Scopus database