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Cyclin A down-regulation in TGF beta 1-arrested follicular lymphoma cells

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11120%2F00%3A00003750" target="_blank" >RIV/00216208:11120/00:00003750 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1006/excr.2000.5047" target="_blank" >http://dx.doi.org/10.1006/excr.2000.5047</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1006/excr.2000.5047" target="_blank" >10.1006/excr.2000.5047</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Cyclin A down-regulation in TGF beta 1-arrested follicular lymphoma cells

  • Original language description

    Transforming growth factor beta1 (TGF beta1) induces growth arrest in many cell types, including B lymphocytes. We examined the effect of TGF on cell cycle progression of a non-Hodgkin lymphoma cell line of follicular lymphoma subtype (FL). After 48 h ofTGF beta1 (10 ng/ml) treatment, a significantly increased number of DoHH2 cells was retained in G(0)/G(1) phase. We examined the level of cell cycle components, cyclins, cyclin-dependent kinases (cdk), and their inhibitors. We found that the expressionof cyclin A and p21(WAF1) molecules was primarily modulated by TGF beta1 treatment while the expression of other regulatory components, like cyclins D, cyclin E, cdk2, cdk4, and cdk6 or p15(INK4B), p16(INK4A), and p27(KIP1) was not significantly affected. We further examined expression and activity of CREB/ATF family members to examine their roles in cyclin A inhibition. The binding activity of CREB-1 and ATF-8 to the CRE region of the cyclin A promoter was almost completely abolished du

  • 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/VS96129" target="_blank" >VS96129: Laboratory of gene expression</a><br>

  • Continuities

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

Others

  • Publication year

    2000

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Experimental Cell Research

  • ISSN

    0014-4827

  • e-ISSN

  • Volume of the periodical

    261

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    10

  • Pages from-to

    250-259

  • UT code for WoS article

    000165622200027

  • EID of the result in the Scopus database