杜立法,刘敬佳,黄鹂,赵勇,王俊杰.125I粒子持续低剂量率照射对人食管癌细胞系KYSE150抑制作用及其机制研究[J].中华放射医学与防护杂志,2014,34(6):415-418
125I粒子持续低剂量率照射对人食管癌细胞系KYSE150抑制作用及其机制研究
The inhibition effects of continuous low dose rate radiation of 125I radioactive seeds on KYSE150 esophageal cancer cells
投稿时间:2013-12-11  
DOI:10.3760/cma.j.issn.0254-5098.2014.06.004
中文关键词:  相对生物学效应  细胞凋亡  G2/M期阻滞  持续低剂量率照射
英文关键词:Relative biological effectiveness  Cell apoptosis  G2/M cell cycle arrest  Continuous low dose rate radiation
基金项目:教育部高等学校博士学科点专项科研基金(20120001110037)
作者单位E-mail
杜立法 100191 北京大学第三医院肿瘤治疗中心  
刘敬佳 100191 北京大学第三医院肿瘤治疗中心  
黄鹂 100191 北京大学第三医院肿瘤治疗中心  
赵勇 中国科学院动物研究所 生物膜与膜生物工程国家重点实验室  
王俊杰 100191 北京大学第三医院肿瘤治疗中心 junjiewang_edu@sina.cn 
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中文摘要:
      目的 研究125I粒子持续低剂量率照射对人食管癌细胞系KYSE150的抑制作用及其机制。方法 根据不同照射方式,将KYSE150细胞分成空白对照组、高剂量率单次外照射组(SDR,1.052 Gy/min)、持续低剂量率照射组(125I-CLDR,2.77 cGy/h)。克隆形成实验衡量KYSE150细胞对两种照射方式的敏感性,计算125I-CLDR的相对生物学效应(RBE)。流式细胞仪分析不同照射方式对细胞凋亡和周期的影响。蛋白免疫印迹法检测不同照射方式下KYSE150细胞内γ-H2AX和Bax的蛋白表达量变化。结果 KYSE150细胞对125I-CLDR的放射敏感性高于SDR,125I-CLDR的相对生物学效应约为1.56;与SDR相比,125I-CLDR能更显著地诱导KYSE150细胞的早期和晚期凋亡(t=4.07,11.08,P<0.05),提高G2/M期细胞比例(t=11.25,P<0.05);125I-CLDR组DNA损伤信号蛋白γ-H2AX和促凋亡蛋白Bax的表达水平显著升高。结论 与SDR相比,125I-CLDR对人食管癌细胞KYSE150的抑制作用更为显著,其主要机制可能是电离辐射后肿瘤细胞克隆形成能力受损,DNA损伤严重,细胞凋亡增多,而G2/M期细胞比例升高,细胞放射敏感性增强。
英文摘要:
      Objective To determine the biological effectiveness of 125I radioactive seeds with continuous low dose rate radiation on the human esophageal cancer cell line KYSE150 in vitro and explore the underlying cellular mechanisms. Methods The cells were divided into three cell groups: control group, single dose radiation group (SDR) and 125I radioactive seeds with continuous low dose rate radiation group (125I-CLDR). The KYSE150 cells were exposed to radiation of X-ray at a high dose rate of 1.052 Gy/min or 125I radioactive seeds at a low dose rate of 2.77 cGy/h. The responses of KYSE150 cells to two modes of irradiation were evaluated by the colony-forming assay, cell apoptosis as well as cell cycle analysis. Furthermore, the expression levels of γ-H2AX and Bax were detected by Western blot. Results KYSE150 cells were more radiosensitive to 125I-CLDR than SDR. The relative biological effectiveness (RBE) for 125I-CLDR related to SDR was 1.56. Compared with SDR, 125I-CLDR yielded more proportions of the early and late apoptosis rate (t=4.07, 11.08, P<0.05) as well as cells at G2/M phase (t=11.25, P<0.05). Moreover, γ-H2AX and Bax expression levels in 125I-CLDR significantly increased compared with SDR. Conclusions Compared with the high dose rate X-ray radiation, the continuous low dose rate radiation of 125I radioactive seeds had stronger inhibition effect on KYSE150 esophageal cancer cells by impairing clonogenic capacity, inducing apoptosis and G2/M cell cycle arrest, and increasing radiosensitivity.
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