093 ± 0.051) were significantly lower than that in blank control group (0.203 ± 0.042) and INCB28060 solubility dmso negative control group (0.210 ± 0.050), respectively (P < 0.05; Figure 1C and 1D), while the difference between blank control group and negative control group was not significant (P > 0.05; Figure 1C and 1D). These data

indicated that JMJD2A-specific siRNA silencing mRNA could significantly reduce the levels of JMJD2A protein expression in MDA-MB-231 cells. Silencing JMJD2A gene resulted in cell cycle changes and proliferation inhibition in MDA-MB-231 cells Cell cycle analysis by FCM revealed that JMJD2A siRNA could induce changes in cell cycle of MDA-MB-231 cells. The mean value of the experiments was shown in Figure 2A, B and 2C. There were no significant differences (P > 0.05) in the percentages of cells at each phase between blank control group and negative

selleck screening library control group. Compared with blank control group (30.3 ± 2.7%) and negative CB-839 control group (34.2 ± 2.3%) respectively, there was a significant difference (P < 0.05) in the percentage of cells in G0/G1 phase in siRNA group (44.3 ± 1.6%). Similarly, there was a significant difference (P < 0.05) in the percentage of cells in S phase in siRNA group (43.4 ± 2.3%), versus blank control group (58.4 ± 2.1%) and negative control group (52.8 ± 2.2%), respectively. However, there was no significant difference (P > 0.05) in the percentage of cells in G2/M phase in siRNA group (12.1 ± 2.2%), relative to blank control group (11.0 ± 1.2%) and negative control group (13.3 ± 1.8%), respectively. Silencing JMJD2A gene could

increase the percentage of cells at G0/G1 phase and decrease the percentage of cells at S phase. The results suggested that HSP90 the treatment could arrest cells at the G1/S checkpoint and delay cell cycle into S phase. Furthermore, proliferation indexes (PI) of each group were calculated. We found that there was a significant difference (P < 0.05) in PI of siRNA group (55.6 ± 2.1%), versus blank control group (69.6 ± 2.1%) and negative control group (65.9 ± 2.2%), respectively. Our results revealed a change in cell cycle with transfection and indicated that cell proliferation could be inhibited by transfection. Figure 2 Knock down of JMJD2A resulted in cell cycle change and proliferation inhibition. A. DNA contents of MDA-MB-231 cells treated in blank control group, negative control group and siRNA group by FCM. B. Column diagram analysis for the percentages of cells at each phase in three different groups: G0/G1 phase, S phase and G2/M phase. At G0/G1 phase, there was a significant difference in the percentage of cells in siRNA group compared with blank control group and negative control group respectively.