Geranylated flavanone tomentodiplacone B inhibits proliferation of human monocytic leukaemia (THP-1) cells
Jazyk angličtina Země Velká Británie, Anglie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
21175584
PubMed Central
PMC3057291
DOI
10.1111/j.1476-5381.2010.01171.x
Knihovny.cz E-zdroje
- MeSH
- akutní monocytární leukemie MeSH
- antikarcinogenní látky farmakologie MeSH
- cyklin D metabolismus MeSH
- cyklin-dependentní kinasa 2 antagonisté a inhibitory biosyntéza metabolismus MeSH
- cykliny metabolismus MeSH
- down regulace účinky léků MeSH
- flavanony farmakologie MeSH
- G1 fáze účinky léků MeSH
- lidé MeSH
- monocyty cytologie účinky léků metabolismus MeSH
- monoterpeny farmakologie MeSH
- nádorové buněčné linie MeSH
- proliferace buněk účinky léků MeSH
- signální transdukce účinky léků MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antikarcinogenní látky MeSH
- CDK2 protein, human MeSH Prohlížeč
- cyklin D MeSH
- cyklin-dependentní kinasa 2 MeSH
- cykliny MeSH
- flavanony MeSH
- monoterpeny MeSH
- tomentodiplacone B MeSH Prohlížeč
BACKGROUND AND PURPOSE: Paulownia tomentosa is a rich source of geranylated flavanones, some of which we have previously shown to have cytotoxic activity. To identify members of this class of compounds with cytostatic effects, we assessed the effects of the geranylated flavanone tomentodiplacone B (TOM B) on cell cycle progression and cell cycle regulatory pathways of THP-1 human monocytic leukaemia cells. EXPERIMENTAL APPROACH: Cell viability was measured by dye exclusion and proliferation by WST-1 assays; cell cycle was monitored by flow cytometry. Regulatory proteins were assessed by immunoprecipitation and kinase assays, and Western blotting. KEY RESULTS: Tomentodiplacone B had no effect during the first 24 h of cell growth at concentrations between 1 and 2.5 µM, but inhibited cell growth in a dose-dependent manner at concentrations of 5 µM or higher. Growth inhibition during the first 24 h of exposure to TOM B was not accompanied by cytotoxicity as cells were accumulated in G1 phase dose-dependently. This G1 phase accumulation was associated with down-regulation of cyclin-dependent kinase 2 activity and also protein levels of cyclins E1 and A2. However, key stress-related molecules (γ-H2AX, p53 and p21) were not induced, suggesting that TOM B acts by directly inhibiting the cyclin-dependent kinase 2 signalling pathway rather than initiating DNA damage or cellular stress. CONCLUSIONS AND IMPLICATIONS: Our study provides the first evidence that TOM B directly inhibits proliferation of human monocytic leukaemia cells, and thus is a potential anticancer agent, preventing leukaemia cells from progressing from G1 phase into DNA synthesis.
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