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Molecular mechanisms of plant steroids and study of their interaction with nuclear receptors in prostate cancer cells

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61389030%3A_____%2F20%3A00524171" target="_blank" >RIV/61389030:_____/20:00524171 - isvavai.cz</a>

  • Alternative codes found

    RIV/61989592:15110/20:73600125 RIV/61989592:15310/20:73600125

  • Result on the web

    <a href="http://doi.org/10.1016/j.fct.2020.111164" target="_blank" >http://doi.org/10.1016/j.fct.2020.111164</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.fct.2020.111164" target="_blank" >10.1016/j.fct.2020.111164</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Molecular mechanisms of plant steroids and study of their interaction with nuclear receptors in prostate cancer cells

  • Original language description

    Plant hormone brassinosteroids (BRs) have multiple important functions in plants. They have also been found to exhibit anti-tumor, anti-angiogenic and anti-proliferative activity. The experimental part of this article describes the effects of BR biosynthetic precursors on prostate cancer cells. The experiments were performed with LNCaP and DU-145 prostate cancer cell lines. These were cultivated and treated with tested BRs in different concentrations and time intervals. The tested compounds were found to affect cell viability, nuclear receptor expression, cell cycle and apoptosis in the tumor cells. IC50 concentrations were determined based on MTT test and the two most active compounds (cathasterone and 6-oxocampestanol) were used in the next experiments. Cathasterone was the most effective of all tested compounds and effectively inhibited integrity of cell spheres. It was found that both BRs had no significant effect on the cell cycle in LNCaP at IC50 concentration, while in DU-145 a significant block in G0/G1 phase after the BR treatment was observed. The effect of BRs on the nuclear steroid receptors was manifested by changes in their expression and localization. BRs demonstrated their significant effect on prostate cancer cells and the compounds have potential used in anticancer drug research and cancer treatment.

  • 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

    10401 - Organic chemistry

Result continuities

  • Project

    <a href="/en/project/GA19-01383S" target="_blank" >GA19-01383S: Modulation of steroid receptors in human cancer cells by brassinosteroids.</a><br>

  • 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

    Food and Chemical Toxicology

  • ISSN

    0278-6915

  • e-ISSN

  • Volume of the periodical

    137

  • Issue of the periodical within the volume

    MAR

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    12

  • Pages from-to

    111164

  • UT code for WoS article

    000517659300024

  • EID of the result in the Scopus database

    2-s2.0-85078850953