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Concepts in MDM2 signaling: allosteric regulation and feedback loops

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00209805%3A_____%2F12%3A%230000290" target="_blank" >RIV/00209805:_____/12:#0000290 - isvavai.cz</a>

  • Result on the web

    <a href="http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3494372/pdf/10.1177_1947601912454140.pdf" target="_blank" >http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3494372/pdf/10.1177_1947601912454140.pdf</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1177/1947601912454140" target="_blank" >10.1177/1947601912454140</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Concepts in MDM2 signaling: allosteric regulation and feedback loops

  • Original language description

    The function and regulation of MDM2 as a component of a p53-dependent negative feedback loop has formed a core paradigm in the p53 field. This concept, now 20 years old, has been solidified by fields of protein science, transgenic technology, and drug discovery in human cancer. However, it has been noted that a simple negative feedback loop between p53 and MDM2 lacks an intrinsic ?activating? step that counteracts this inhibition and permits oscillation of the feedback to occur as p53 is switched on andoff. More recent work has identified a solution to the missing piece of the picture that counters the negative feedback loop, which is MDM2 itself. Under conditions of genotoxic stress, MDM2 helps to activate p53 by increasing its rate of protein synthesis. This simple observation makes certain aspects of the p53 response more comprehensible such as why MDM2 is upregulated by p53 early on following DNA damage and how phosphorylation of MDM2 at the C-terminal Ser395 by ATM translates int

  • 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

    <a href="/en/project/ED2.1.00%2F03.0101" target="_blank" >ED2.1.00/03.0101: Regional Centre for Applied Molecular Oncology (RECAMO)</a><br>

  • Continuities

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

Others

  • Publication year

    2012

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Genes and cancer

  • ISSN

    1947-6019

  • e-ISSN

  • Volume of the periodical

    3

  • Issue of the periodical within the volume

    3-4

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    7

  • Pages from-to

    291-297

  • UT code for WoS article

  • EID of the result in the Scopus database