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Histone deacetylase inhibitors for the treatment of cancer stem cells

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61389030%3A_____%2F16%3A00469858" target="_blank" >RIV/61389030:_____/16:00469858 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1039/c6md00297h" target="_blank" >http://dx.doi.org/10.1039/c6md00297h</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/c6md00297h" target="_blank" >10.1039/c6md00297h</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Histone deacetylase inhibitors for the treatment of cancer stem cells

  • Original language description

    Tiny populations of tumor cells are present in solid and hematologic malignancies and are responsible for cancer development, metastasis and limited response to therapy; these are referred to as cancer stem cells (CSCs). CSCs are resistant to standard cancer treatments and are the main cause of tumor relapse. Therefore, the development of new therapeutics to overcome the resistance of CSCs is greatly required. It is known that epigenetic histone modifications (acetylation/deacetylation) play a crucial role in cancer development through regulation of gene expression. Deacetylation of histone and non-histone proteins controls cell proliferation, metabolism and apoptosis as well as DNA repair and differentiation. Thus, histone deacetylase inhibitors (HDACis) are a promising group of anti-cancer agents, showing the ability to induce growth arrest or apoptosis in tumor cells. In this review, we summarize the current knowledge about the prospects of HDACis utilization in the treatment of CSCs.

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    CC - Organic chemistry

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/LD14128" target="_blank" >LD14128: Synthesis of sirtuin inhibitors</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2016

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    MedChemComm

  • ISSN

    2040-2503

  • e-ISSN

  • Volume of the periodical

    7

  • Issue of the periodical within the volume

    12

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    15

  • Pages from-to

    2217-2231

  • UT code for WoS article

    000390552300002

  • EID of the result in the Scopus database