He Min, Jiang Yu-Yan, Zhu Miao, Wei Xiao, Qin Jian, Zhang Zhi-Yong, Li Li
Medical Scientific Research Center, Guangxi Medical University, Nanning, Guangxi, 530021, P. R. China.
Ai Zheng. 2006 May;25(5):543-8.
BACKGROUND & OBJECTIVE: The mechanism of inhibiting telomerase activity by telomerase inhibitors is very complex, and involves common actions of many proteins. This study was to investigate the effects of 3'-azido-deoxythymidine (AZT) on telomerase activity and protein expression of hepatocarcinoma cell line SMMC-7721, and explore possible mechanism of inhibiting telomerase activity in SMMC-7721 cells by AZT.
Optimized concentration and treatment time of AZT were detected by MTT assay. After treatment with AZT, the telomerase activity in SMMC-7721 cells was detected by real-time fluorescent quantitative TRAP (FQ-TRAP) assay; the apoptosis of SMMC-7721 cells was detected by TUNEL assay and flow cytometry (FCM); the changes of specific proteins were monitored by raman spectra assay and surface-enhanced laser desorption time of flight-mass spectrum (SELDI-TOF-MS) with protein chip assay.
The optimized treatment time of AZT was 48 h, and the optimized concentration of AZT was 20 mmol/L. When treated with 20 mmol/L AZT for 48 h, the telomerase activity in SMMC-7721 cells was inhibited by 53.85% of control (P<0.001); apoptotic morphologic changes of SMMC-7721 cells were observed; the apoptosis rate of SMMC-7721 cells was 13.5%; 7 spectral peak of proteins were changed; 24 proteins were up-regulated and 8 were down-regulated in SMMC-7721 cells. All of the 32 distinct proteins were small molecular proteins.
AZT can inhibit the telomerase activity and induce apoptosis of SMMC-7721 cells, which is related to specific small molecular proteins.
端粒酶抑制剂抑制端粒酶活性的机制非常复杂,涉及多种蛋白质的共同作用。本研究旨在探讨3'-叠氮脱氧胸苷(AZT)对肝癌细胞系SMMC-7721端粒酶活性及蛋白表达的影响,探讨AZT抑制SMMC-7721细胞端粒酶活性的可能机制。
采用MTT法检测AZT的最佳作用浓度和作用时间。用AZT处理后,采用实时荧光定量TRAP(FQ-TRAP)法检测SMMC-7721细胞的端粒酶活性;采用TUNEL法和流式细胞术(FCM)检测SMMC-7721细胞的凋亡情况;采用拉曼光谱法和表面增强激光解吸飞行时间质谱(SELDI-TOF-MS)结合蛋白质芯片法监测特异性蛋白的变化。
AZT的最佳作用时间为48 h,最佳作用浓度为20 mmol/L。当用20 mmol/L AZT处理48 h时,SMMC-7721细胞的端粒酶活性被抑制至对照组的53.85%(P<0.001);观察到SMMC-7721细胞出现凋亡形态学改变;SMMC-7721细胞的凋亡率为13.5%;7个蛋白光谱峰发生改变;SMMC-7721细胞中有24个蛋白上调,8个蛋白下调。所有32种不同的蛋白均为小分子蛋白。
AZT可抑制SMMC-7721细胞的端粒酶活性并诱导其凋亡,这与特异性小分子蛋白有关。