中华放射医学与防护杂志
中華放射醫學與防護雜誌
중화방사의학여방호잡지
Chinese Journal of Radiological Medicine and Protection
2014年
6期
415-418
,共4页
杜立法%刘敬佳%黄鹂%赵勇%王俊杰
杜立法%劉敬佳%黃鸝%趙勇%王俊傑
두입법%류경가%황리%조용%왕준걸
相对生物学效应%细胞凋亡%G2/M期阻滞%持续低剂量率照射
相對生物學效應%細胞凋亡%G2/M期阻滯%持續低劑量率照射
상대생물학효응%세포조망%G2/M기조체%지속저제량솔조사
Relative biological effectiveness%Cell apoptosis%G2/M cell cycle arrest%Continuous low dose rate radiation
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(125 I-CLDR,2.77 cGy/h).克隆形成实验衡量KYSEI50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(=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.
目的 研究125I粒子持續低劑量率照射對人食管癌細胞繫KYSE150的抑製作用及其機製.方法 根據不同照射方式,將KYSE150細胞分成空白對照組、高劑量率單次外照射組(SDR,1.052 Gy/min)、持續低劑量率照射組(125 I-CLDR,2.77 cGy/h).剋隆形成實驗衡量KYSEI50細胞對兩種照射方式的敏感性,計算125I-CLDR的相對生物學效應(RBE).流式細胞儀分析不同照射方式對細胞凋亡和週期的影響.蛋白免疫印跡法檢測不同照射方式下KYSE150細胞內γ-H2AX和Bax的蛋白錶達量變化.結果 KYSE150細胞對125I-CLDR的放射敏感性高于SDR,125I-CLDR的相對生物學效應約為1.56;與SDR相比,125I-CLDR能更顯著地誘導KYSE150細胞的早期和晚期凋亡(=4.07,11.08,P<0.05),提高G2/M期細胞比例(t=11.25,P<0.05);125I-CLDR組DNA損傷信號蛋白γ-H2AX和促凋亡蛋白Bax的錶達水平顯著升高.結論 與SDR相比,125I-CLDR對人食管癌細胞KYSE150的抑製作用更為顯著,其主要機製可能是電離輻射後腫瘤細胞剋隆形成能力受損,DNA損傷嚴重,細胞凋亡增多,而G2/M期細胞比例升高,細胞放射敏感性增彊.
목적 연구125I입자지속저제량솔조사대인식관암세포계KYSE150적억제작용급기궤제.방법 근거불동조사방식,장KYSE150세포분성공백대조조、고제량솔단차외조사조(SDR,1.052 Gy/min)、지속저제량솔조사조(125 I-CLDR,2.77 cGy/h).극륭형성실험형량KYSEI50세포대량충조사방식적민감성,계산125I-CLDR적상대생물학효응(RBE).류식세포의분석불동조사방식대세포조망화주기적영향.단백면역인적법검측불동조사방식하KYSE150세포내γ-H2AX화Bax적단백표체량변화.결과 KYSE150세포대125I-CLDR적방사민감성고우SDR,125I-CLDR적상대생물학효응약위1.56;여SDR상비,125I-CLDR능경현저지유도KYSE150세포적조기화만기조망(=4.07,11.08,P<0.05),제고G2/M기세포비례(t=11.25,P<0.05);125I-CLDR조DNA손상신호단백γ-H2AX화촉조망단백Bax적표체수평현저승고.결론 여SDR상비,125I-CLDR대인식관암세포KYSE150적억제작용경위현저,기주요궤제가능시전리복사후종류세포극륭형성능력수손,DNA손상엄중,세포조망증다,이G2/M기세포비례승고,세포방사민감성증강.
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 (125 I-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.