ABSTRACT
Objective To investigate the effect and mechanism of boron neutron capture therapy(BNCT) in C6 glioma cell line.Methods C6 cells in exponential phase were divided into 6 groups: untreated control,(~(60)Co?)(4 Gy),~(60)Co? 8 Gy,nuclear reactor exposure without boronophenylalanine(BPA) 3 Gy,BNCT(4 Gy) and BNCT 8 Gy.Cellular morphological change was observed by an inverted microscope,light microscope,fluorescence microscope and electronic microscope.Flow cytometry was used to determine the percentage of apoptosis,necrosis and normal cells 48h after irradiation.Colony forming assay was used to calculate cell surviving fraction.Results Typical morphological changes of apoptosis were observed early after irradiation in BNCT group,with a significant increase in apoptotic rates was observed 48 h after irradiation with 63.2% and 88.3% for BNCT(4 Gy) and 8 Gy group,respectively(P
ABSTRACT
Objective To evaluate the incorporation of BPA, which was synthesized by ourselves, by two different glioma cell lines, and to observe its relationship with the time of cultivation and cell cycle. Methods Two glioma cell lines of C6 and SHG-44 were studied and the primarily cultured rat astrocytes were used as control. The growth curves of the two glioma cell lines and rat astrocytes were plotted, and their doubling time was identified respectively from the curves. All three kinds of cells were incubated in a culture medium, in which 10 B concentration was 50?g/ml for 4h, 8h, 16h, 20h or 24h. Boron concentration in the cells was measured by induced couple plasma atomic emission spectroscopy (ICP-AES) after respective culture period. After 24h of incubation, the cells in the G 0 /G 1 phase and those in the G 2 /M phase were isolated by flow cytometry, and boron concentration in each fraction was obtained by ICP-AES. Results The doubling time was 18.5h for both C6 and SHG-44 cells, but 28h for the astrocytes. The boron concentration in glioma cells was constantly higher than that in astrocytes throughout the experiment(P
