高级搜索
青蒿琥酯对人肺腺癌A549细胞中caspase-9及caspase-3活性的影响[J]. 肿瘤防治研究, 2007, 34(09): 651-653. DOI: 10.3971/j.issn.1000-8578.2020
引用本文: 青蒿琥酯对人肺腺癌A549细胞中caspase-9及caspase-3活性的影响[J]. 肿瘤防治研究, 2007, 34(09): 651-653. DOI: 10.3971/j.issn.1000-8578.2020
Apoptosis Induced by Artesunate in Human Adenocarcinoma Cell Line A549 Cells Associated with Activation of caspase-9 and caspase-3[J]. Cancer Research on Prevention and Treatment, 2007, 34(09): 651-653. DOI: 10.3971/j.issn.1000-8578.2020
Citation: Apoptosis Induced by Artesunate in Human Adenocarcinoma Cell Line A549 Cells Associated with Activation of caspase-9 and caspase-3[J]. Cancer Research on Prevention and Treatment, 2007, 34(09): 651-653. DOI: 10.3971/j.issn.1000-8578.2020

青蒿琥酯对人肺腺癌A549细胞中caspase-9及caspase-3活性的影响

Apoptosis Induced by Artesunate in Human Adenocarcinoma Cell Line A549 Cells Associated with Activation of caspase-9 and caspase-3

  • 摘要: 目的 研究青蒿琥酯(artesunate,Art)体外诱导人肺腺癌A549细胞凋亡及对半胱天冬氨酸蛋白酶9(cysteine containing aspartate9,caspase-9)和caspase-3活性的影响。方法 Art处理A549细胞,流式细胞计数(Flow Cytometry,FCM)检测细胞周期和细胞凋亡,比色法检测caspase-9活性,westernblot检测caspase-3变化。结果 FCM显示A549细胞经100mg/L Art作用24h,出现S期细胞减少(P〈0.01),G2/M期细胞数目增多(P〈0.01),细胞凋亡率增加(P〈0.0)。不同浓度(10mg/L、25mg/L、50mg/L、100mg/L)的Art作用A549细胞24h,caspase-9活性呈浓度依赖性增加,分别为对照组的9.87倍、23.33倍(P〈0.01)、38.47倍(P〈0.01)和60.47倍(P〈0.01)。Western blot显示A549细胞经100mg/L Art作用6、12、24h后,细胞浆中caspase-3活化,分别为对照组1.2倍、1.6倍(P〈0.01)、1.8倍(P〈0.01)。结论 青蒿琥酯可通过增加caspase-9和caspase-3的活性,诱导A549细胞凋亡,为阐明Art的抗癌机理,指导青蒿琥酯用于肿瘤治疗提供实验依据。

     

    Abstract: Objective To investigate the effects of artesunate on apoptosis of human adenocarcinoma cell line A549 cells and activation of cysteine containing aspartate 9(caspase-9) and cysteine containing aspartate 3(caspase-3). Methods A549 cells were treated with artesunate, cell cycle phase's distribution and apoptosis were detected by flow cytometry. Activation of caspase-9 was identified by colorimetric assay. Change of caspase-3 was detected by western blot. Results With artesunate treatment, marked cell accumul...

     

/

返回文章
返回