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Effects of paclitaxel, docetaxel and their combinations on subcutaneous lymphomas in inbred Sprague-Dawley/Cub rats

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60077344%3A_____%2F06%3A00053543" target="_blank" >RIV/60077344:_____/06:00053543 - isvavai.cz</a>

  • Alternative codes found

    RIV/68378050:_____/06:00053543 RIV/00216208:11110/06:00005430 RIV/75010330:_____/06:00007057

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Effects of paclitaxel, docetaxel and their combinations on subcutaneous lymphomas in inbred Sprague-Dawley/Cub rats

  • Original language description

    We investigated whether the effects on paclitaxel, docetaxel or their combinations on T-cell lymphomas in Sprague-Dawley/Cub rats were mainly caused by their different efficiency or combination of different mechanism of action, or limited by metabolic inactivation by P450 enzymes or drug efflux caused by P-glycoprotein. Docetaxel most effectively prolonged the survival of rats and the time of lymphoma appearance, inhibited their intravital size and weight after sacrifice. Paclitaxel was poorly effectiveand combined administration had intermediate effects. Docetaxel was 3-fold more effective than paclitaxel against P388D1 lymphoma cell line used as a model and combined action was dominated by the effects of docetaxel. Thus, docetaxel was effective against T-cell lymphomas and may be a potential anticancer drug in similar indications.

  • Czech name

    Účinky paclitaxelu, docetaxelu a jejich kombinace na podkožní lymfomy u inbredních krys Sprague-Dawley/Cub

  • Czech description

    Sledovali jsme, zda účinky paclitaxelu, docetaxelu či jejich kombinací na T-buněčné lymfomy v krysách Sprague-Dawley/Cub závisejí na jejich odlišné účinnosti nebo na kombinaci různých mechanismů jejich účinku, omezení metabolickou inaktivací enzymů P450,či snížení koncentrace léčiva vyvolaném P-glykoproteinem. Docetaxel nejúčinněji prodlužoval přežití krys a dobu do vzniku lymfomů, jejichž velikost a hmotnost omezoval. Paclitaxel byl málo účinný a v kombinaci byl účinek obou léků středního rozsahu. Namodelovou linii lymfomu P388D1 působil docetaxel 3x více než paclitaxel a v kombinaci obou léčiv převládal jeho účinek. Docetaxel je tedy účinným prostředkem proti T-buněčným lymfomům a lze ho využít při protinádorové léčbě tohoto typu.

Classification

  • Type

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

  • CEP classification

    EB - Genetics and molecular biology

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/NL7567" target="_blank" >NL7567: Effect of polyphenols and chelators on toxicity and effects of anthracyclines and taxanes</a><br>

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2006

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    European Journal of Pharmaceutical Sciences

  • ISSN

    0928-0987

  • e-ISSN

  • Volume of the periodical

    29

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    9

  • Pages from-to

    442-450

  • UT code for WoS article

  • EID of the result in the Scopus database