氧化苦参碱通过P38MAPK通路抑制人宫颈癌HeLa细胞增殖  被引量:7

Inhibitory effect of oxymatrine on human cervical carcinoma He La cell proliferation through P38 MAPK signaling pathways

在线阅读下载全文

作  者:刘晶[1] 李菁菁[2] 李义飞[1] 葛静[1] 滑芳[1] 谢磊[1] 李林[1] 孟亚丽[1] 

机构地区:[1]河北医科大学第一医院妇产科,河北石家庄050031 [2]河北医科大学细胞生物教研室,河北石家庄050051

出  处:《中国现代医学杂志》2015年第10期10-14,共5页China Journal of Modern Medicine

基  金:河北省卫生厅重点科技研究计划(No:20110049)

摘  要:目的观察氧化苦参碱(OXY)对人宫颈癌HeLa细胞增殖的影响,并探讨其机制及作用。方法人宫颈癌HeLa细胞经过系列浓度的OXY(1.0、2.0和4.0mg/ml)处理不同时间后,采用噻唑蓝(MTT)法测定细胞增殖的变化。免疫印迹(Westernblot)方法测定OXY对HeLa细胞PCNA、CyclinD1和P38MAPK、P-P38MAPK计学意义表达的影响。并采用AnnexinV-PI双染测定细胞凋亡。结果氧化苦参碱成浓度时间依赖性抑制HeLa细胞增殖;高浓度氧化苦参碱(4.0mg/ml)不仅抑制HeLa细胞增殖,而且促进细胞凋亡。与对照组比,OXY处理细胞的PCNA和CyclinD1蛋白表达明显降低(P<0.05,P<0.01),而P-P38MAPK蛋白表达水平明显升高;P38MAPK特异性抑制剂可缓解OXY对HeLa细胞增殖的抑制率,增加PCNA和CyclinD1蛋白表达。结论OXY能够通过提高P38MAPK磷酸化而下调PCNA和CyclinD1表达,抑制HeLa细胞增殖。[ Objective ] To investigate the inhibitory effect of oxymatrine (OXY) on the human cervical carcinoma HeLa cell proliferation through the P38 MAPK signaling pathways. [Methods] HeLa cells were cultured in RPMI 1640 medium. MTT assay was used to determine cell proliferation. PCNA, Cyclin D1, P38 MAPK, P-P38 MAPK protein expressions were tested by western blot. Apoptosis was detected by Annexin V-PI double staining. [ Results ] OXY inhibited the proliferation of HeLa cells in a concentration and time dependent manner. Compared with control group, the expressions of PCNA, Cyclin D1 protein were significantly lower in OXY group (P 〈 0.05, P 〈 0.01), and the expression of P-P38 MAPK was significantly higher in OXY group (P 〈 0.01). The expression of PCNA, Cyclin D1 were significantly higher, while P-P38 MAPK were significantly lower in OXY + SB203580 group than those in OXY group (P 〈 0.01). [Conclusions] OXY can inhibit HeLa cell proliferation and down-regulate PCNA and Cyclin D1 expressions by activating P-P38 MAPK pathway.

关 键 词:氧化苦参碱 人宫颈癌 P38MAPK 

分 类 号:R711[医药卫生—妇产科学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象