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Lipoxygenase inhibitors enhance tumor suppressive effects of Jun proteins v-myb-transformed monoblasts BM2

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    SYSNO ASEP0127049
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JOstatní články
    TitleLipoxygenase inhibitors enhance tumor suppressive effects of Jun proteins v-myb-transformed monoblasts BM2
    Author(s) Bryja, V. (CZ)
    Sedláček, J. (CZ)
    Zahradníčková, E. (CZ)
    Ševčíková, S. (CZ)
    Pacherník, Jiří (BFU-R)
    Souček, Karel (BFU-R) RID, ORCID
    Hofmanová, Jiřina (BFU-R) RID, ORCID
    Kozubík, Alois (BFU-R) RID, ORCID
    Šmarda, J. (CZ)
    Source TitleProstaglandins - ISSN 0090-6980
    Roč. 72, 3-4 (2003), s. 131-145
    Number of pages15 s.
    Languageeng - English
    CountryUS - United States
    Keywordshematopoiesis ; arachidonic acid ; lipoxygenase inhibitors
    Subject RIVBO - Biophysics
    R&D ProjectsGA301/01/0040 GA ČR - Czech Science Foundation (CSF)
    GA524/03/0766 GA ČR - Czech Science Foundation (CSF)
    CEZAV0Z5004920 - BFU-R
    AnnotationInhibitors of arachidonic acid (AA) conversion were described as suppressors of proliferation and inducers of differentiation of various leukemic cells. Certain AA metabolites have been shown to cooperate with Jun proteins that are important factors controlling cell proliferation, differentiation and apoptosis. Using lipoxygenase (LOX) inhibitors of various specifity we studied possible participation of lipoxygenase pathway in regulation of proliferation and apoptosis of v-myb-transformed chicken monoblasts BM2 and its functional interaction with Jun proteins. We found that nordihydroguaiaretic acid (NDGA) and esculetin (Esc) negatively regulate proliferation of BM2 cells causing accumulation in either G(0)/G(1)-phase (nordihydroguaiaretic acid) or S-phase (esculetin) of the cell cycle. BM2 cells can be also induced to undergo growth arrest and partial differentiation by ectopic expression of Jun proteins.
    WorkplaceInstitute of Biophysics
    ContactJana Poláková, polakova@ibp.cz, Tel.: 541 517 244
    Year of Publishing2004

Number of the records: 1  

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