Song Dong-po, Lin Ju-sheng, Fu Gui-lian, Sun Xue-mei, Kong Xin-juan, Li Pei-yuan, Ma Xin
Institute of Liver Diseases, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Zhonghua Gan Zang Bing Za Zhi. 2004 Oct;12(10):616-9.
To construct vector pEGFP-C1-hTERT-ribozyme (pGTRz-U6) and its mutant (pGTmRz-U6) against hTERT containing U6 promoter, then transfect them into human liver cancer cell line SMMC7721 to observe the action of the human telomerase catalytic subunit (hTERT) hammerhead ribozyme on proliferation and apoptosis of human liver cancer cell SMMC7721.
Eukaryotic expressing vector pGTRz-U6 and mutant pGTmRz-U6 were constructed and transfected into SMMC7721 using Lipofectamine2000 Reagent, with pEGFP-C1 as the control group. After strict screening by G418, positive clones were cultured; the amount of expression of ribozyme and hTERT was detected by RT-PCR; cell proliferation by MTT; telomerase activity by TRAP and silver staining assay; cell apoptosis by FCM.
We found that the two ribozymes were expressed persistently in SMMC7721; different expression levels (P < 0.01) of hTERT among SMMC7721-Rz, SMMC7721-mRz and SMMC7721-pEGFP-C1 was exhibited by the analysis of variance with SPSS software. The difference between SMMC7721-Rz and the others is significant in t-test (P < 0.01), while there was no difference between SMMC7721-mRz and SMMC7721-pEGFP-C1 (P > 0.05). With the advance of cell division, telomerase activities of the cells treated by SMMC7721-Rz and SMMC7721-mRz decreased gradually, and the percentage of apoptosis of the cells transfected with Rz and mRz increased gradually. The apoptosis percentage of 7PDS SMMC7721-Rz was 29.86%, while those of SMMC7721-mRz and SMMC7721-pEGFP-C1 were 9.87% and 3.36%, respectively.
The apoptosis level of SMMC7721 induced by hTERT ribozyme increases as cells divide, and this ribozyme maybe a potential approach for liver cancer gene therapy.
构建含U6启动子的针对人端粒酶逆转录酶(hTERT)的载体pEGFP-C1-hTERT-核酶(pGTRz-U6)及其突变体(pGTmRz-U6),并将其转染入人肝癌细胞系SMMC7721,观察人端粒酶催化亚基(hTERT)锤头状核酶对人肝癌细胞SMMC7721增殖和凋亡的作用。
构建真核表达载体pGTRz-U6和突变体pGTmRz-U6,用Lipofectamine2000试剂将其转染入SMMC7721,以pEGFP-C1作为对照组。经G418严格筛选后,培养阳性克隆;用RT-PCR检测核酶和hTERT的表达量;用MTT检测细胞增殖;用TRAP和银染法检测端粒酶活性;用流式细胞术检测细胞凋亡。
发现两种核酶在SMMC7721中持续表达;用SPSS软件进行方差分析显示,SMMC7721-Rz、SMMC7721-mRz和SMMC7721-pEGFP-C1中hTERT的表达水平不同(P<0.01)。t检验显示SMMC7721-Rz与其他组之间差异有统计学意义(P<0.01),而SMMC7721-mRz与SMMC7721-pEGFP-C1之间无差异(P>0.05)。随着细胞分裂的进行,SMMC7721-Rz和SMMC7721-mRz处理组细胞的端粒酶活性逐渐降低,转染Rz和mRz的细胞凋亡率逐渐升高。SMMC7721-Rz组的凋亡率为29.86%,而SMMC7721-mRz和SMMC7721-pEGFP-C1组分别为9.87%和3.36%。
hTERT核酶诱导的SMMC7721细胞凋亡水平随细胞分裂而升高,该核酶可能是肝癌基因治疗的一种潜在方法。