浙江医学
浙江醫學
절강의학
ZHEJIANG MEDICAL JOURNAL
2013年
7期
510-512
,共3页
SKP2%p27kip1%鼻咽癌%放射疗法%细胞周期
SKP2%p27kip1%鼻嚥癌%放射療法%細胞週期
SKP2%p27kip1%비인암%방사요법%세포주기
SKP2%p27kip1%Nasopharyngeal carcinoma%Radiation%Cel cycle
目的探讨SKP2、p27kip1及细胞周期阻滞在放疗后鼻咽癌细胞应答中的作用.方法以人鼻咽低分化鳞癌CNE2细胞株作为研究对象,流式细胞仪检测放疗前后细胞周期变化,West blot检测放疗前后不同时间点SKP2及p27kip1表达的变化.结果放疗后鼻咽癌CNE2细胞株出现G2/M期细胞周期阻滞,低剂量(2Gy)放疗后0.5~1.5h出现SKP2表达短暂下降,同时伴p27kip1表达相应增高;放疗后4h出现SKP2表达升高而p27kip1表达下调.高剂量(6Gy)放疗后1.5h内出现SKP2表达升高,而放疗后2~4h表达下降;而p27kip1表达在放疗后0.5h出现短暂下降,1.5~4h表达上调,两者之间关联性不确定.结论 SKP2、p27kip1和细胞周期阻滞参与放疗后鼻咽癌CNE2细胞的应答反应,且低剂量放疗时,p27kip1表达可能受SKP2调控.
目的探討SKP2、p27kip1及細胞週期阻滯在放療後鼻嚥癌細胞應答中的作用.方法以人鼻嚥低分化鱗癌CNE2細胞株作為研究對象,流式細胞儀檢測放療前後細胞週期變化,West blot檢測放療前後不同時間點SKP2及p27kip1錶達的變化.結果放療後鼻嚥癌CNE2細胞株齣現G2/M期細胞週期阻滯,低劑量(2Gy)放療後0.5~1.5h齣現SKP2錶達短暫下降,同時伴p27kip1錶達相應增高;放療後4h齣現SKP2錶達升高而p27kip1錶達下調.高劑量(6Gy)放療後1.5h內齣現SKP2錶達升高,而放療後2~4h錶達下降;而p27kip1錶達在放療後0.5h齣現短暫下降,1.5~4h錶達上調,兩者之間關聯性不確定.結論 SKP2、p27kip1和細胞週期阻滯參與放療後鼻嚥癌CNE2細胞的應答反應,且低劑量放療時,p27kip1錶達可能受SKP2調控.
목적탐토SKP2、p27kip1급세포주기조체재방료후비인암세포응답중적작용.방법이인비인저분화린암CNE2세포주작위연구대상,류식세포의검측방료전후세포주기변화,West blot검측방료전후불동시간점SKP2급p27kip1표체적변화.결과방료후비인암CNE2세포주출현G2/M기세포주기조체,저제량(2Gy)방료후0.5~1.5h출현SKP2표체단잠하강,동시반p27kip1표체상응증고;방료후4h출현SKP2표체승고이p27kip1표체하조.고제량(6Gy)방료후1.5h내출현SKP2표체승고,이방료후2~4h표체하강;이p27kip1표체재방료후0.5h출현단잠하강,1.5~4h표체상조,량자지간관련성불학정.결론 SKP2、p27kip1화세포주기조체삼여방료후비인암CNE2세포적응답반응,차저제량방료시,p27kip1표체가능수SKP2조공.
@@@@Objective To investigate the expression of SKP2 and p27kip1 in the cel ular response to radiation in human na-sopharyngeal carcinoma cel s CNE-2. Methods The expressions of SKP2 and p27kip1 in human nasopharyngeal carcinoma CNE-2 cel s were detected by Western blot before and after ionizing radiation. Flow cytometry was used for cel cycle Analysis. Results The CNE2 cel s displayed a G2/M cel-cycle arrest after exposure to radiation. Western blot analysis showed a transient increasd expression of p27kip1 and decreased expression of Skp2 at 0.5~1.5h after exposure to low doses ionizing radiation (2Gy);meanwhile 2~4h after exposure to low dose radiation the expression of Skp2 was up-regulated and p27kip1 down-regulated. However, the expressions pattern of SKP2 and p27kip1 were reversed to above observation after exposure to high doses ionizing radiation (6Gy). Conclusion The results suggest that SKP2 may contribute to the regulation of p27kip1 and may be a key factor in regulating the cel cycle in response to radiation-induced DNA damage.