Effects of cyclopamine on the proliferation and cycle of prostate cancer cell line DU145
SUN Quan-wu
ZHOU Feng-hai
WANG Yang-min
CHI Qiang
Abstract:Objective:To investigate the inhibitory effect of the Hedgehog signal pathway blocker (cyclopamine) on DU145 cells. Methods:We interfered DU145 cells with cyclopamine at the concentrations of 1,10,50 and 100 μmol/L and detected its inhibitory effect on the cells by MTT colorimetry assay at 24,48 and 72 hours,as well as its effect on the cell cycle by flow cytometry. We also determined the difference in the mRNA expression of cyclin E between the experimental and control groups by RT-PCR at 48 hours after 50 μmol/L cyclopamine intervention. Results:Cyclopamine inhibited the DU145 cells in a time- and dose-dependent manner,with inhibition rates of 7.42,12.70 and 59. 15% in the 10,50 and 100 μmol/L groups respectively at 24 hours,significantly different from that of the blank control group ( P < 0.05). It markedly suppressed the proliferation of the DU145 cells at > 10 μmol/L at 24 hours. Flow cytometry showed an obviously increased proportion of stage Cl cells at the concentration of > 10 μmol/L after 48-hour intervention,with statistically significant differences from the Cl cell proportions in the control,10μmol/L and 50 (μmol/ L groups,which were (52.17 ± 2.21)%,(60.13 ± 2.75)% and (74.30 ± 3.52)% respectively (P<0.01). The apoptoticpeak was elevated with the increased concentration of cyclopamine. The cyclin E mRNA expression of the DU14S cells was decreased by 61.90% at 48 hours after 50μmol/L cyclopamine intervention as compared with the blank control group (P < 0.01). Conclusion :Cyclopamine can inhibit the proliferation of DU145 cells,and the mechanism may be related with its effect of down-regulating the cyclin E mRNA expression of DU145 cells and blocking them in stage G1. Cyclopamine can also induce the apoptosis of DU145 cells.
Keywords:cyclopamineprostate cancerDU145 cellHedgehog signal pathwaycell cycle
Publication Date:2010-03-02
Online Publishing Date:2025-08-15(First online date of this platform, not the publication date of the document)
Pages:5( 227-231 )
