冬凌草甲素对人胰腺癌SW1990细胞系生长抑制作用  被引量:22

The inhibitory effect of oridonin on human pancreas adenocarcinoma SW1990 cells

在线阅读下载全文

作  者:宋芳[1,2] 冯一中[2] 蒋小岗[1] 顾振纶[1] 郭次仪[1] 

机构地区:[1]苏州中药研究所,江苏苏州215007 [2]苏州大学医学院病理学教研室,江苏苏州215123

出  处:《中国药理学通报》2010年第2期240-243,共4页Chinese Pharmacological Bulletin

基  金:香港保健协会研究资助项目(No20070908-7HK)

摘  要:目的研究冬凌草甲素(oridonin)对人胰腺癌SW1990细胞生长抑制作用并探究其可能机制。方法采用MTT法检测冬凌草甲素对SW1990细胞增殖抑制作用、Hoechst 33258染色法及透射电镜观察细胞的形态学变化、流式细胞仪检测细胞周期及凋亡率、RT-PCR法检测survivin、p21mR-NA表达。结果冬凌草甲素对人胰腺癌SW1990细胞具有明显的生长抑制作用,荧光显微镜和透射电镜下均见到典型的凋亡形态学改变,流式分析出现亚G1峰并显示G2/M期周期阻滞。RT-PCR分析结果显示p21mRNA表达增加而survivin mRNA表达减少。结论冬凌草甲素通过诱导凋亡和G2/M期周期阻滞来抑制人胰腺癌SW1990细胞生长,其分子机制可能与survivin和p21调节的信号途径有关。Aim To study the inhibitory effects and its mechanisms of oridonin on human pancreas adenoeareinoma SW1990 cells. Methods Cell growth inhibition mediated by oridonin on SW1990cells was measured by MTT assay. The morphological changes were observed by Hoeehst33258 fluoroehrome staining and electron microscope. Cell cycle and apoptosis rate were analyzed by flow eytometry. The molecular mechanisms involved in the effects of oridonin on SW1990 cells were studied by RT-PCR. Results The growth of humen pancreas adenocarcinoma SW1990 cells was significantly inhibited by ofidonin. Apoptosis morphological changes about chromatic agglutination and nuclear condensation were detected by Hoechst 33258 fluorochrome staining and electron microscope in oridonin treated SW1990 cells. "Sub-G1 " phase peak and G2/M growth arrest werer found with flow cytometry. The upregulating mRNA ex- pression of p21 and downregulating mRNA expression of survivin were detected by RT-PCR. Conclusion The inhibitory effect of oridonin on human pancreas adenocarcinoma SW1990 cells through induced apoptosis and G2/M growth arrest and the mechanisms may be through surviving-p21 co-regluation pathway.

关 键 词:冬凌草甲素 SW1990细胞 凋亡 周期阻滞 SURVIVIN P21 

分 类 号:R284.1[医药卫生—中药学] R329.25[医药卫生—中医学]

 

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