中国老年学杂志
中國老年學雜誌
중국노년학잡지
CHINESE JOURNAL OF GERONTOLOGY
2015年
10期
2601-2603
,共3页
甘生敏%罗超%李娟%刘双%李亚军%李少林%彭志平
甘生敏%囉超%李娟%劉雙%李亞軍%李少林%彭誌平
감생민%라초%리연%류쌍%리아군%리소림%팽지평
盐霉素%鼻咽癌%放疗%敏感性
鹽黴素%鼻嚥癌%放療%敏感性
염매소%비인암%방료%민감성
Salinomycin%Nasopharyngeal carcinoma%Radiation therapy%Sensitivity
目的:探讨盐霉素对低分化鼻咽癌干细胞放疗敏感性的影响。方法将鼻咽癌干细胞悬液放入标有1~24的孔板中培养,其中1~12为对照组,13~24为实验组,其中向对照组加入200μl的PBS缓冲液,向实验组加入200μl终浓度为2μmol/L的盐霉素,适宜环境中培养12 h后,两组细胞均给予6 Gy单次照射,放疗结束后,接种至培养皿中常规培养2 w,GIEMSA染色,计算细胞存活分数(SF),采用 RT-PCR及 Western 印迹法检测选取培养24 h后人鼻咽癌干细胞中Rad51、Ku70、Ku80基因及蛋白表达水平。结果实验组培养皿中细胞SF明显低于对照组( P<0.05)。实验组培养皿鼻咽癌干细胞Rad51、Ku70和Ku80 mRNA表达水平低于对照组(P<0.05)。实验组培养皿鼻咽癌干细胞 Rad51、Ku70和Ku80蛋白表达水平明显低于对照组(P<0.05)。结论盐霉素能够明显抑制人低分化鼻咽癌干细胞中 Rad51、Ku70和 Ku80表达,降低细胞存活分数,提高放疗敏感性和临床疗效。
目的:探討鹽黴素對低分化鼻嚥癌榦細胞放療敏感性的影響。方法將鼻嚥癌榦細胞懸液放入標有1~24的孔闆中培養,其中1~12為對照組,13~24為實驗組,其中嚮對照組加入200μl的PBS緩遲液,嚮實驗組加入200μl終濃度為2μmol/L的鹽黴素,適宜環境中培養12 h後,兩組細胞均給予6 Gy單次照射,放療結束後,接種至培養皿中常規培養2 w,GIEMSA染色,計算細胞存活分數(SF),採用 RT-PCR及 Western 印跡法檢測選取培養24 h後人鼻嚥癌榦細胞中Rad51、Ku70、Ku80基因及蛋白錶達水平。結果實驗組培養皿中細胞SF明顯低于對照組( P<0.05)。實驗組培養皿鼻嚥癌榦細胞Rad51、Ku70和Ku80 mRNA錶達水平低于對照組(P<0.05)。實驗組培養皿鼻嚥癌榦細胞 Rad51、Ku70和Ku80蛋白錶達水平明顯低于對照組(P<0.05)。結論鹽黴素能夠明顯抑製人低分化鼻嚥癌榦細胞中 Rad51、Ku70和 Ku80錶達,降低細胞存活分數,提高放療敏感性和臨床療效。
목적:탐토염매소대저분화비인암간세포방료민감성적영향。방법장비인암간세포현액방입표유1~24적공판중배양,기중1~12위대조조,13~24위실험조,기중향대조조가입200μl적PBS완충액,향실험조가입200μl종농도위2μmol/L적염매소,괄의배경중배양12 h후,량조세포균급여6 Gy단차조사,방료결속후,접충지배양명중상규배양2 w,GIEMSA염색,계산세포존활분수(SF),채용 RT-PCR급 Western 인적법검측선취배양24 h후인비인암간세포중Rad51、Ku70、Ku80기인급단백표체수평。결과실험조배양명중세포SF명현저우대조조( P<0.05)。실험조배양명비인암간세포Rad51、Ku70화Ku80 mRNA표체수평저우대조조(P<0.05)。실험조배양명비인암간세포 Rad51、Ku70화Ku80단백표체수평명현저우대조조(P<0.05)。결론염매소능구명현억제인저분화비인암간세포중 Rad51、Ku70화 Ku80표체,강저세포존활분수,제고방료민감성화림상료효。
Objective To investigate the effects of salinomycin on radiation sensitivity of low differentiation nasopharyngeal carcino -ma stem cells.Methods Nasopharyngeal carcinoma stem cell suspension were put into orifice plate marked with 1~24, plated with1~12 were selected as the control group, with 13~24 were selected as the experimental group.200μl PBS were added into control group, 200μl salinomycin ( concentration was 2 μmol/L) were added into experimental group.Cells were cultured into suitable environment for 12 h, and were given 6 Gy single radiation therapy.After radiation therapy, cells were cultured into petri dish for 2 weeks.Cell survival fraction ( SF) was calculated by GIEMSA staining, Rad51, Ku70, Ku80 gene and protein expression were detected by RT-PCR and Western blot after cul-tured 24 h.Results SF in experimental group was lower than that of control group (P<0.05).Expression of Rad51, Ku70, Ku80 mRNA in experimental group were lower than those of control group (P<0.05).Expression of Rad51, Ku70, Ku80 protein in experimental group were lower than those of control group (P<0.05).Conclu sions Salinomycin could significantly inhibit the expressions of Rad51, Ku70 and Ku80 in low differentiation nasopharyngeal carcinoma cells, reduce the SF, improve radiation sensitivity and clinical curative effect.