Effect of dexamethasone combined with oridonin on proliferation and apoptosis of multiple myeloma cell line U266
10.3760/cma.j.issn.1009-9921.2016.10.002
- VernacularTitle:冬凌草甲素联合地塞米松对多发性骨髓瘤U266细胞增殖及凋亡的影响
- Author:
Qilin ZHAN
;
Fuhong WU
;
Long ZHU
;
Jun LI
;
Weiyun JIN
- Publication Type:Journal Article
- Keywords:
Multiple myeloma;
Oridonin;
Dexamethasone;
Proliferation;
Apoptosis
- From:
Journal of Leukemia & Lymphoma
2016;25(10):582-587
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the effect of dexamethasone combined with oridonin on proliferation and apoptosis in multiple myeloma cells U266 and the related molecular mechanism. Methods Exponential phase of growth U266 cells were treated with different concentrations of oridonin combined with dexamethasone or alone. U266 cells treated by DMSO were taken as control group. The proliferation inhibitory ratios were measured by CCK-8 assay followed by 24 h, 48 h and 72 h. Apoptosis induction was assessed by using Annexin V-FITC kit. Real time PCR was used to examine the mRNA changes of Notch1, NF-κB/p65 and bcl-2. Western blot assay was applied to detect the protein expression of Notch1, cleaved Notch1, NF-κB/p65 and bcl-2. Results Compared with that in control group, proliferation in all the experimental groups was inhibited (P<0.05), and the apoptosis was promoted (P<0.05); especially the combination of dexamethasone and oridonin had a synergistic effect on the proliferation and apoptosis of U266 cells (P<0.05). The results of PCR and Western blot showed that after treatment of U266 cells with dexamethasone, the mRNA as well as their protein levels of NF-κB/p65 and bcl-2 were decreased compared with those in the control group (P<0.05). Moreover, the mRNA and protein expression of Notch1, cleaved Notch1, NF-κB/p65 and bcl-2 was obviously down-regulated in oridonin group and the combination group (P<0.05). Conclusion Combination of dexamethasone and oridonin can significantly increase the anti-tumor effect by inhibiting proliferation and inducing apoptosis of U266 cells, which may be related to the inhibition of the Notch1 pathway.
