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Potential Clinical Uses of CDK Inhibitors: Lessons from Synthetic Lethality Screens

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F15%3A33157602" target="_blank" >RIV/61989592:15310/15:33157602 - isvavai.cz</a>

  • Alternative codes found

    RIV/61389030:_____/15:00450910

  • Result on the web

    <a href="http://onlinelibrary.wiley.com/doi/10.1002/med.21354/epdf" target="_blank" >http://onlinelibrary.wiley.com/doi/10.1002/med.21354/epdf</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/med.21354" target="_blank" >10.1002/med.21354</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Potential Clinical Uses of CDK Inhibitors: Lessons from Synthetic Lethality Screens

  • Original language description

    Developments in genetic and genomic technology have produced vast quantities of data that are gradually yielding new insights into fundamental cellular and molecular processes. In particular, they have revealed some differences between normal and transformed cells that could potentially be exploited to develop targeted, personalized cancer therapies with unprecedented efficiencies. This review summarizes recent findings from synthetic lethality (SL) screens against cyclin-dependent kinases (CDKs) that can be targeted with small molecule kinase inhibitors. SL screens can be used to identify cancers sensitive to CDK inhibitors. Several SL partners of specific CDKs have been identified, including MYC, K-Ras, VHL, PI3K, and PARP, all of which are discussedin the review. CDK inhibitors have been in clinical trials for nearly 20 years and it has become clear that effective therapy using these compounds will require careful selection of patients with respect to the specific molecular phenoty

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    CE - Biochemistry

  • OECD FORD branch

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

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

    Medicinal Research Reviews

  • ISSN

    0198-6325

  • e-ISSN

  • Volume of the periodical

    35

  • Issue of the periodical within the volume

    6

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    19

  • Pages from-to

    1156-1174

  • UT code for WoS article

    000362795200003

  • EID of the result in the Scopus database