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The biological activity of G-quadruplex DNA binding papaverine-derived ligand in breast cancer cells
Authors:Blazej Rubis  Mariusz Kaczmarek  Natalia Szymanowska  Elzbieta Galezowska  Andrzej Czyrski  Bernard Juskowiak  Tadeusz Hermann  Maria Rybczynska
Affiliation:(1) Department of Clinical Chemistry and Molecular Diagnostics, Poznan University of Medical Sciences, Przybyszewskiego 49, 60-355 Poznan, Poland;(2) Department of Clinical Immunology, Poznan University of Medical Sciences, Rokietnicka 5d, 60-806 Poznan, Poland;(3) Laboratory of Analytical Chemistry, Faculty of Chemistry, Adam Mickiewicz University in Poznan, Grunwaldzka 6, 60-780 Poznan, Poland;(4) Department of Physical Pharmacy and Pharmacokinetics, Poznan University of Medical Sciences, ul. Święcickiego 6, 60-781 Poznan, Poland;
Abstract:
Summary  It was shown previously that the papaverine oxidation products 6a,12a-diazadibenzo-[a,g]fluorenylium derivative (ligand 1) and 2,3,9,10-tetramethoxy-12-oxo-12H-indolo[2,1-a]isoquinolinium chloride (ligand 2) bind to guanine-quadruplexes (G4) of single stranded G-rich 3′-overhangs of mammalian telomeric DNA. Here we show the biological activity of ligand 1. This compound exhibit antiproliferative activity in MCF-7 cells (IC50 for ligand 1 = 14.16 ± 0.01 μM, 24 h, 1.158 ± 0.056 μM, 72 h. PCNA levels were not altered after treatment of MCF-7 cells with concentrations of ligand 1 which, however, led to alterations in the cell cycle. 5 and 10 μM of the ligand 1 arrested cells in the G0/G1 phase of the cell cycle and this led to a decrease of cells in the S phase. Intracellular accumulation of ligand 1 was observed even after a cell passage and medium exchange in fluorescence microscopy while low concentrations of ligand 1 (0.001 to 0.1 μM) inhibited telomerase activity as shown by TRAP assay.
Keywords:Papaverine derivative  Cell cycle arrest  Breast cancer  Telomerase inhibitor  DNA binding  G-quadruplex DNA
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