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作 者:郭永[1] 何森[1,2] 苏晨[1,3] 王乾兴[3] 邹检平[1]
机构地区:[1]国家人口计生委科学技术研究所,北京100081 [2]沈阳药科大学生命科学与生物制药学院 [3]遵义医学院细胞生物学与遗传学教研室
出 处:《中国计划生育学杂志》2014年第5期300-303,共4页Chinese Journal of Family Planning
基 金:中央级公益性科研院所基本科研专项基金(2010GJSSJKA04);北京市自然科学基金资助项目(7132160)
摘 要:目的:研究米非司酮促进乳腺癌T47D细胞凋亡的作用。方法:根据米非司酮的处理浓度分为0.25μmol/L组、2.5μmol/L组、25μmol/L组和50μmol/L组,各组分别加入相应浓度米非司酮处理人乳腺癌T47D细胞2d后,采用末端脱氧核苷酸转移酶介导的dUTP缺口末端标记测定法检测细胞凋亡,在荧光显微镜下观察绿色荧光细胞数量和荧光强度,采用膜联蛋白V-异硫氰酸荧光素/碘化吡啶法在流式细胞仪上检测凋亡细胞百分率。结果:25μmol/L组和50μmol/L组与对照组比较,阳性绿色荧光细胞的数量更多,荧光强度更强;25μmol/L组和50μmol/L组的凋亡细胞百分比(分别为16.1±3.5%和17.2±3.8%)高于对照组(5.1±2.3%),差异有统计学意义(分别为P=0.010和P=0.009);0.25μmol/L组和2.5μmol/L组的凋亡细胞百分比与对照组比较差异无统计学意义(分别为P=0.818和P=0.884)。结论:米非司酮能够促进乳腺癌T47D细胞的凋亡,且随着米非司酮剂量的升高,凋亡细胞数量增加。Objective: To investigate the promoting effect of mifepristone on the apoptosis of human breast cancer cells T47D in vitro. Methods: T47D cells were treated by different concentrations (0.25, 2.5, 25 and 50μmol/L) of mife- pristone. Then the apoptosis of these cells was examined by TUNEL assay under the microscope on day 2. The apopto- sis was also examined by Annexin V--FITC assay. Results: Compared with the control group, the number and intensi- ties of the TUNEL--positive cells in 25μmol/L group and 50μmol/L group were significantly higher and stronger. The apoptosis rates of 25μmol/L group (16.1±3.5%, P=0.010) and 50μmol/L group (17.2±3.8%, P=0.009) were sig- nificantly higher than that of the control group (5.1 ± 2.3 % ). There were no significant differences between the control group and 0.25μmol/L group (P=0.818) as well as 2.5μmol/L group (P =0.884). Conclusion: Mifepristone can in- duce the apoptosis of T47D cells in a dose--dependent manner.
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