张 卓, 邹丽娟, 田莹莹①. β-榄香烯乳联合照射对肺腺癌A549 细胞凋亡及KU70基因表达的影响*[J]. 中国肿瘤临床, 2010, 37(4): 184-186. DOI: 10.3969/j.issn.1000-8179.2010.04.002
引用本文: 张 卓, 邹丽娟, 田莹莹①. β-榄香烯乳联合照射对肺腺癌A549 细胞凋亡及KU70基因表达的影响*[J]. 中国肿瘤临床, 2010, 37(4): 184-186. DOI: 10.3969/j.issn.1000-8179.2010.04.002
ZHANG Zhuo1, ZOU Lijuan1, TIAN Yingying2. Effect of β-elemene Combined with Radiotherapy on the Expression of KU70 mRNA and Apoptosis of Lung Adenocarcinoma Cell Line A549[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2010, 37(4): 184-186. DOI: 10.3969/j.issn.1000-8179.2010.04.002
Citation: ZHANG Zhuo1, ZOU Lijuan1, TIAN Yingying2. Effect of β-elemene Combined with Radiotherapy on the Expression of KU70 mRNA and Apoptosis of Lung Adenocarcinoma Cell Line A549[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2010, 37(4): 184-186. DOI: 10.3969/j.issn.1000-8179.2010.04.002

β-榄香烯乳联合照射对肺腺癌A549 细胞凋亡及KU70基因表达的影响*

Effect of β-elemene Combined with Radiotherapy on the Expression of KU70 mRNA and Apoptosis of Lung Adenocarcinoma Cell Line A549

  • 摘要: 目的:检测β- 榄香烯乳对肺腺癌A549 细胞株放射增敏作用,探讨β- 榄香烯乳影响细胞凋亡及KU70基因mRNA 表达的放射增敏机制。方法:四氮唑蓝比色分析法(MTT 法)检测β- 榄香烯乳对A549 细胞的半数抑制浓度(IC 50);将细胞分为对照组(C)、照射组(IR)、β- 榄香烯乳组(0.1 ×IC50、0.2 ×IC50)及β- 榄香烯乳联合照射组(0.1 ×IC50+IR、0.2 ×IC50+IR),不同浓度的β- 榄香烯乳处理细胞24h 后照射,通过克隆形成实验计算细胞存活率;流式细胞仪检测细胞周期与凋亡率;逆转录PCR 技术(RT-PCR)检测细胞KU70基因mRNA 表达量。结果:MTT 法测得β-榄香烯乳对A549 细胞的IC 50值为120 μ g/mL;克隆形成实验证明β-榄香烯乳对A549 细胞有放射增敏作用;β- 榄香烯乳联合照射组细胞G2/M期比率及凋亡率明显高于单纯照射组及β- 榄香烯乳组(P<0.05);β- 榄香烯乳联合照射组细胞KU70基因mRNA 表达量较照射组明显下降(P<0.05)。 结论:β- 榄香烯乳可促进A549 细胞凋亡和抑制KU70基因mRNA 表达,诱导凋亡同时抑制KU70参与的双链损伤修复途径可能是其放射增敏的机制。

     

    Abstract: Objective: To study the effect of β-elemene combined wi th radiotherapy on the expression of KU70mRNA and apoptosis of lung adenocarcinoma cell line A 549 . Methods:A549 cells were divided into the control group (c), irridation group (IR), β-elemene group (0.1 × IC 50and 0.2 × IC 50i.e. 10μ g/mL and 20μ g/mL β-elemene ) and β-elemene combined with irridation group (0.1 × IC 50+ IR and 0.2 × IC 50+ IR). IC 50was obtained through MTT method and cell survival rate was analyzed by colony formation test. Cell cycle and apoptosis were detected with flow cytometry. The expression level of KU70mRNA was detected by RT-PCR.Results: MTT assay showed that IC50value of A 549 cells was 120 μ g/mL. The number of cel l clones and survival rate of β-elemene groups were decl ined signi ficantly. The radiosensi tivi ty of A549 cells can be enhanced by β-elemene. The flow cytometry confi rmed that the ratio of G2/M and apoptosis were significantly in-creased under the effect of β-elemene, statistical ly di fferent from those in the control group (P <0.05). The expression level of KU70 mRNA in β-elemene wi th radiotherapy group was decl ined signi ficantly, statistical ly di fferent from those in the con-trol group (P <0.05). Conclusion:The radiosensi tization effect of β-elemene on A549 cells is associated with induction of cell apoptosis and down-regulation of KU70mRNA expression.

     

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