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作 者:白艳丽[1] 龚卫锋[1] 王兆龙[1] 李静[1] 李珊[1] 刘志新[2] 张献清[2]
机构地区:[1]西安市中心医院输血科,陕西西安710003 [2]第四医大学西京医院输血科,陕西西安710032
出 处:《中国医学物理学杂志》2010年第1期1676-1680,共5页Chinese Journal of Medical Physics
基 金:陕西省科学技术研究发展计划项目课(NO.2008K09-09)
摘 要:目的:观察低剂量辐射外周血单个核细胞联合棉酚衍生物ApoG2对体外培养人前列腺癌PC-3细胞的杀伤作用。方法:采用1Gyγ射线照射人外周血单个核细胞,辐射剂量率为17Gy/min,实验设对照组、照射及未照射的外周血单个核细胞与PC-3细胞共培养组、ApoG2处理组及照射的外周血单个核细胞与ApoG2联合作用组。利用吖啶橙/溴化乙啶(AO/EB)荧光双染色法及MTT法,观察外周血单个核细胞和/或ApoG2对肿瘤细胞的杀伤情况。结果:辐照的外周血单个核细胞及ApoG2处理组对PC-3的杀伤作用明显增强,杀伤活性明显高于未辐照组(P<0.05),而联合作用组的杀伤活性明显高于辐照组及ApoG2处理组((P<0.01)。结论:低剂量辐射外周血单个核细胞联合ApoG2可以明显提高其体外的抗肿瘤效应。Objective: To observe the killing effect of irradiated peripheral blood mononuclear cells (PBMCs) at low dose combined with apogossypolone (ApoG2) on cultured human prostate cancer PC-3 cells. Methods: Human PBMCs were irradated by gamma my at 1 gray,the irradiation dose rate was 17 Gy/min.The experiment were divided into PC-3 tumor cell control group,PC-3 cells with irradiated and non-irradiated PBMCs co-culture groups, ApoG2 treatment group, irradiated PBMCs and ApoG2 co-treatment group.Acridine orange/ethidium bromide (AO/EB) staining and MTT method were used to observe the killing effect of PBMCs and/or ApoG2. Results: The killing activity of irradiated PBMCs group and ApoG2 treatment group were obviously increased and were higher than that of non-irradiated group (P〈O.05). The killing activityof combined group were much higher than that of irradiated group and ApoG2 treatment group (P 〈0.01). Conclusion: Irradiated PBMCs at low dose combined with ApoG2 can enhances the anti-tumor effects markedly.
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