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Decitabine and SAHA-induced apoptosis is accompanied by survivin downregulation and potentiated by ATRA in p53-deficient cells

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023736%3A_____%2F14%3A00011143" target="_blank" >RIV/00023736:_____/14:00011143 - isvavai.cz</a>

  • Result on the web

    <a href="http://www.hindawi.com/journals/omcl/2014/165303/" target="_blank" >http://www.hindawi.com/journals/omcl/2014/165303/</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1155/2014/165303" target="_blank" >10.1155/2014/165303</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Decitabine and SAHA-induced apoptosis is accompanied by survivin downregulation and potentiated by ATRA in p53-deficient cells

  • Original language description

    While p53-dependent apoptosis is triggered by combination of methyltransferase inhibitor decitabine (DAC) and histone deacetylase inhibitor suberoylanilide hydroxamic acid (SAHA) in leukemic cell line CML-T1, reactive oxygen species (ROS) generation as well as survivin and Bcl-2 deregulation participated in DAC + SAHA-induced apoptosis in p53-deficient HL-60 cell line. Moreover, decrease of survivin expression level is accompanied by its delocalization from centromere-related position in mitotic cells suggesting that both antiapoptotic and cell cycle regulation roles of survivin are affected by DAC + SAHA action. Addition of subtoxic concentration of all-trans-retinoic acid (ATRA) increases the efficiency of DAC + SAHA combination on viability, apoptosis induction, and ROS generation in HL-60 cells but has no effect in CML-T1 cell line. Peripheral blood lymphocytes from healthy donors showed no damage induced by DAC + SAHA + ATRA combination.

  • 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

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

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

    Oxidative medicine and cellular longevity

  • ISSN

    1942-0900

  • e-ISSN

  • Volume of the periodical

    2014

  • Issue of the periodical within the volume

    [July]

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    14

  • Pages from-to

    "art. no. 165303"

  • UT code for WoS article

    000340289700001

  • EID of the result in the Scopus database