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Targeting the Checkpoint to Kill Cancer Cells

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F15%3A10317646" target="_blank" >RIV/00216208:11310/15:10317646 - isvavai.cz</a>

  • Alternative codes found

    RIV/68378050:_____/15:00455240

  • Result on the web

    <a href="http://www.mdpi.com/2218-273X/5/3/1912" target="_blank" >http://www.mdpi.com/2218-273X/5/3/1912</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3390/biom5031912" target="_blank" >10.3390/biom5031912</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Targeting the Checkpoint to Kill Cancer Cells

  • Original language description

    Cancer treatments such as radiotherapy and most of the chemotherapies act by damaging DNA of cancer cells. Upon DNA damage, cells stop proliferation at cell cycle checkpoints, which provides them time for DNA repair. Inhibiting the checkpoint allows entry to mitosis despite the presence of DNA damage and can lead to cell death. Importantly, as cancer cells exhibit increased levels of endogenous DNA damage due to an excessive replication stress, inhibiting the checkpoint kinases alone could act as a directed anti-cancer therapy. Here, we review the current status of inhibitors targeted towards the checkpoint effectors and discuss mechanisms of their actions in killing of cancer cells.

  • Czech name

  • Czech description

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/GA14-34264S" target="_blank" >GA14-34264S: Role of R2TP complex in DNA damage response and cell proliferation</a><br>

  • Continuities

    S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2015

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Biomolecules [online]

  • ISSN

    2218-273X

  • e-ISSN

  • Volume of the periodical

    5

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    26

  • Pages from-to

    1912-1937

  • UT code for WoS article

    000362504200034

  • EID of the result in the Scopus database