摘要
采用 RT- PCR自小鼠脾细胞 RNA中扩增出鼠 TRAIL 基因的全长 c DNA,利用 DNA重组技术将其插入到真核表达载体 pc DNA3.1中获得重组质粒 p X1。经酶切鉴定及序列分析 ,表明成功构建 TRAIL 的真核表达质粒。通过直接肌肉内注射进行基因转染 ,p X1具有诱导肝癌细胞凋亡、抑制肝癌生长的作用。表明 TRAIL
The mouse TRAIL cDNA was amplified from the RNA of the mouse spleen cells by using RT PCR and cloned into the eukaryotic expressing vector pcDNA3 by DNA recombinant technique to obtain the recombinant plasmid pX1. The eukaryotid expressing plasmid pX1 was constructed successfully which was confirmed by enzyme cleavage identification and sequencing identification. The transfection of plasmid pX1 by injection into muscle of mouse could produce the inhibitory effect on liver carcinoma growth by inducing cells into apoptosis. It was demonstrated that TRAIL could be applied into the gene therapy for liver carcinoma as a direct killing mechanism.
出处
《华中科技大学学报(医学版)》
CAS
CSCD
北大核心
2002年第6期618-620,共3页
Acta Medicinae Universitatis Scientiae et Technologiae Huazhong
基金
国家自然科学基金资助项目 (No. 39870 76 3)
教育部跨世纪人才培养计划基金资助项目(教技厅 - 1997
2号文)
关键词
TRAIL
凋亡诱导配体
肝癌
基因治疗
TNF related apoptosis inducing ligand
liver carcinoma
gene therapy