中国医学创新
中國醫學創新
중국의학창신
MEDICAL INNOVATION OF CHINA
2014年
22期
11-14
,共4页
姚祺%刘冠环%姜清%张国然%袁伟%林云
姚祺%劉冠環%薑清%張國然%袁偉%林雲
요기%류관배%강청%장국연%원위%림운
丹参酮ⅡA%肝癌%凋亡%XIAP
丹參酮ⅡA%肝癌%凋亡%XIAP
단삼동ⅡA%간암%조망%XIAP
TanshinoneⅡA%Hepatocellular carcinoma%Apoptosis%XIAP
目的:探讨丹参酮ⅡA对肝癌细胞中凋亡抑制蛋白XIAP的影响。方法:通过MTT实验、流式细胞术、细胞形态观察检测丹参酮ⅡA对细胞增殖和凋亡的影响,通过蛋白免疫印迹的方法检测丹参酮ⅡA对细胞中凋亡抑制蛋白XIAP、凋亡蛋白caspase-3以及PARP蛋白的影响。结果:MTT、细胞形态结果显示丹参酮ⅡA对SMMC-7721细胞的生长抑制作用成时间和剂量依赖性,免疫印迹结果显示,0.5μg/mL丹参酮ⅡA作用肝癌细胞24 h后,caspase-3前体、凋亡抑制蛋白XIAP表达明显下调,活化的caspase-3、剪切形式的PARP含量显著增加。结论:丹参酮ⅡA下调凋亡抑制蛋白XIAP,活化caspase-3,促进PARP剪切诱导肝癌细胞凋亡。
目的:探討丹參酮ⅡA對肝癌細胞中凋亡抑製蛋白XIAP的影響。方法:通過MTT實驗、流式細胞術、細胞形態觀察檢測丹參酮ⅡA對細胞增殖和凋亡的影響,通過蛋白免疫印跡的方法檢測丹參酮ⅡA對細胞中凋亡抑製蛋白XIAP、凋亡蛋白caspase-3以及PARP蛋白的影響。結果:MTT、細胞形態結果顯示丹參酮ⅡA對SMMC-7721細胞的生長抑製作用成時間和劑量依賴性,免疫印跡結果顯示,0.5μg/mL丹參酮ⅡA作用肝癌細胞24 h後,caspase-3前體、凋亡抑製蛋白XIAP錶達明顯下調,活化的caspase-3、剪切形式的PARP含量顯著增加。結論:丹參酮ⅡA下調凋亡抑製蛋白XIAP,活化caspase-3,促進PARP剪切誘導肝癌細胞凋亡。
목적:탐토단삼동ⅡA대간암세포중조망억제단백XIAP적영향。방법:통과MTT실험、류식세포술、세포형태관찰검측단삼동ⅡA대세포증식화조망적영향,통과단백면역인적적방법검측단삼동ⅡA대세포중조망억제단백XIAP、조망단백caspase-3이급PARP단백적영향。결과:MTT、세포형태결과현시단삼동ⅡA대SMMC-7721세포적생장억제작용성시간화제량의뢰성,면역인적결과현시,0.5μg/mL단삼동ⅡA작용간암세포24 h후,caspase-3전체、조망억제단백XIAP표체명현하조,활화적caspase-3、전절형식적PARP함량현저증가。결론:단삼동ⅡA하조조망억제단백XIAP,활화caspase-3,촉진PARP전절유도간암세포조망。
To investigate the effect of inhibitor of apoptosis protein XIAP in hepatocellular carcinoma cells treated with TanshinoneⅡA.Method:Effect of TanshinoneⅡA on cell proliferation and apoptosis were determined by MTT test,flow cytometry and cell morphology observation.The effects of TanshinoneⅡA on inhibitor of apoptosis protein XIAP,apoptosis related proteins procaspase-3 and PARP protein in cells were measured by Western blot.Result:MTT,cell morphology results showed that TanshinoneⅡA inhibited the growth of SMMC-7721 cells in a dose and time dependent manner,Western blotting results showed that 0.5μg/mL tanshinoneⅡA in hepatocellular carcinoma cells after 24 h,Caspase-3 precursor,inhibitor of apoptosis protein XIAP expression were down regulated,the content of PARP,caspase-3 splicing activation increased significantly.Conclusion:Tanshinone ⅡA can down regulate XIAP protein,activate caspase-3 and promote PARP shear,and induce apoptosis of hepatocellular carcinoma cells.