摘要
目的:本文探讨三氧化二砷(Arsenictrioxide,As2O3)对人肺癌细胞株A2放射敏感性的影响。方法:设立空白对照组、单纯照射组(直线加速器X射线照射,2 Gy)、As2O3组(1.0μmol/LAs2O3)、As2O3+照射组(1.0μmol/LAs2O3+X射线照射,2 Gy)。用流式细胞仪检测As2O3作用后肿瘤细胞周期的变化,MTT法及平板克隆形成试验测定各实验组人肺癌细胞株A2细胞存活分数和集落形成率,用流式细胞仪观察Bcl-2蛋白的表达。结果:As2O3作用后使A2细胞出现明显G2/M期阻滞。As2O3+照射组细胞存活分数和集落形成率较As2O3组及单纯照射组明显下降,与As2O3组或单纯照射组比较差异具有显著性(P<0.01)。As2O3+照射组细胞Bcl-2蛋白的表达明显下调,与As2O3组或单纯照射组比较差异具有显著性(P<0.01)。结论:As2O3对人肺癌细胞A2具有放射增敏作用,其增敏机制可能与As2O3增加照射前G2/M期细胞比例及照射后肿瘤细胞的凋亡率有关。
Objective:To explore the effect of arsenic trioxide on radiosensitivity in human lung cancer cell line A2.Methods: There were four groups in the study:control group(untreated group),As2O3 group(1.0 μmol/L As2O3),irradiation group,As2O3+ irradiation group.Cellular response to irradiation was evaluated by the colony forming test and MTT assay;Flow cytometry was used to determined the Bcl-2 protein expression and cell cycle.Results: As2O3 could induced a G2/M cell cycle arrest.As2O3 + irradiation could significantly decreased the proliferation rate(vs As2O3 group or irradiation group,P0.01).As2O3 significantly decreased the expression of Bcl-2 in irradiated human lung cancer cell line A2(vs As2O3 group or irradiation group,P0.01).Conclusion: Arsenic trioxide could sensitize the human lung cancer cell A2 to ionizing irradiation.This effect is probably caused by increasing the rate of G2/M cells before irradiation and the apoptosis rate of A2 cells after irradiation.
出处
《重庆医科大学学报》
CAS
CSCD
北大核心
2011年第2期156-159,共4页
Journal of Chongqing Medical University
基金
重庆市卫生局科研基金项目(编号:2008-2-31)