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作 者:胡荣[1] 李佳[1] 李迎春[1] 杨莹[1] 朱珂[1] 苗苗[1] 廖爱军[1] 杨威[1] 刘卓刚[1]
机构地区:[1]中国医科大学附属盛京医院血液科,辽宁沈阳110004
出 处:《现代肿瘤医学》2014年第3期509-512,共4页Journal of Modern Oncology
基 金:辽宁省科学技术厅资助项目(编号:2010225032)
摘 要:目的:探讨Embelin增加HL-60细胞对肿瘤坏死因子相关凋亡诱导配体(TRAIL)的敏感性及可能的作用机制。方法:TRAIL 1、5、10、50及100 ng/ml分别处理HL-60细胞6、12、24及48h,MTT法绘制细胞生长曲线;TRAIL 10 ng/ml±亚细胞毒浓度的Embelin处理HL-60细胞6、12、24及48h,Annexin V/PI复染流式细胞术检测细胞凋亡,Western blot检测24h时Caspase-3、8及9的表达;亚细胞毒浓度的Embelin处理HL-60细胞6、12、24及48h,实时荧光定量PCR检测DR4及DR5 mRNA的表达。结果:TRAIL对HL-60细胞具有增殖抑制作用。亚细胞毒浓度的Embelin联合10 ng/ml TRAIL作用于HL-60细胞时细胞凋亡率较单独应用TRAIL时增加,相应的Caspase-3、8及9的表达也随之增加。结论:亚细胞毒浓度的Embelin可以增加HL-60细胞对TRAIL的敏感性,其机制可能与上调DR4及DR5 mRNA表达并进而启动凋亡途径有关。Objective:To investigate whether Embelin could sensitize HL-60 cells to TRAIL or not and explore the possible mechanism. Methods:HL- 60 cells were treated with TRAIL of 1,5,10,50 and 100 ng/ml for 6,12,24 and 48h seperatedly and proliferation curve was plotted by MTT assay. HL - 60 cells were treated with 10ng/ml TRAIL with or without Embelin of subtoxic concentration for 6,12,24 and 48h seperatedly,and cell apoptosis rate was detected by Annexin V/PI double staining and flow cytometry and Caspase - 3,8 and 9 at 24h by Western blot. HL - 60 cells were treated with Embelin of subtoxic concentration for 6,12,24 and 48h seperatedly,and DR4 and DR5 mR- NA were detected by real - time PCR. Results:TRAiL inhibited HL - 60 cells proliferation. TRAIL combined with Embelin of subtoxic concentration was more effective in inducing cell apoptosis than TRAIL alone and Caspase - 3,8 and 9 expression increase correspondingly. Conclusion: Embelin of subtoxic concentration could sensitize HL -60 cells to TRAIL. Upregulation of DR4 and DR5 mRNA and initiation of apoptosis pathway may contribute to the possi- ble mechanism.
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