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硫氧还蛋白还原酶反义RNA对人肝癌细胞生长的抑制作用

Inhibitory effects of thioredoxin reductase antisense RNA on the growth of human hepatocellular carcinoma cells.

作者信息

Gan Lu, Yang Xiang-Liang, Liu Qiong, Xu Hui-Bi

机构信息

College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan 430074,China.

出版信息

J Cell Biochem. 2005 Oct 15;96(3):653-64. doi: 10.1002/jcb.20585.

DOI:10.1002/jcb.20585
PMID:16088946
Abstract

Thioredoxin reductase (TrxR) in conjunction with thioredoxin (Trx) is a ubiquitous intracellular oxidoreductase system with antioxidant and redox regulatory roles. In some human tumors, the thioredoxin system is found overexpressed. We have used an antisense approach to investigate whether inhibition of TrxR overexpression can suppress the growth of human hepatocellular carcinoma SMMC-7721 cells. TrxR cDNA fragment was inserted in the antisense direction into pcDNA3.1/myc-His and SMMC-7721 cells were stably transfected with the plasmid construct. The results showed that TrxR antisense RNA could significantly reduce TrxR mRNA level and activity, and suppress the growth of SMMC-7721 cells. Cell-cycle analysis showed G2/M phase arrest in SMMC-7721 cells transfected with TrxR antisense plasmid. TrxR antisense RNA could significantly increase p53 mRNA level and decrease Bcl-2 mRNA level by reverse transcriptase-polymerase chain reaction (RT-PCR). Furthermore a significant decrease in human telomerase reverse transcriptase (hTERT) mRNA level was found in SMMC-7721 cells transfected with TrxR antisense plasmid. Flow cytometry and telomere fluorescence in situ hybridization (Flow FISH) showed that TrxR antisense RNA could significantly reduce the telomere fluorescence in SMMC-7721 cells. The results suggested that TrxR antisene RNA inhibited the growth of SMMC-7721 cells through an accumulation of cell cycle at G2/M phase, an increase in p53 mRNA level and a reduction in telomere fluorescence and Bcl-2, hTERT mRNA levels.

摘要

硫氧还蛋白还原酶(TrxR)与硫氧还蛋白(Trx)共同构成了一种普遍存在的细胞内氧化还原酶系统,具有抗氧化和氧化还原调节作用。在一些人类肿瘤中,硫氧还蛋白系统呈现过表达。我们采用反义技术来研究抑制TrxR过表达是否能抑制人肝癌SMMC - 7721细胞的生长。将TrxR cDNA片段以反义方向插入pcDNA3.1/myc - His载体,并用该质粒构建体稳定转染SMMC - 7721细胞。结果显示,TrxR反义RNA能显著降低TrxR mRNA水平和活性,并抑制SMMC - 7721细胞的生长。细胞周期分析表明,转染TrxR反义质粒的SMMC - 7721细胞出现G2/M期阻滞。通过逆转录 - 聚合酶链反应(RT - PCR)发现,TrxR反义RNA能显著提高p53 mRNA水平,并降低Bcl - 2 mRNA水平。此外,在转染TrxR反义质粒的SMMC - 7721细胞中,人端粒酶逆转录酶(hTERT)mRNA水平显著降低。流式细胞术和端粒荧光原位杂交(Flow FISH)表明,TrxR反义RNA能显著降低SMMC - 7721细胞中的端粒荧光。结果提示,TrxR反义RNA通过使细胞周期在G2/M期积累、提高p53 mRNA水平、降低端粒荧光以及Bcl - 2和hTERT mRNA水平来抑制SMMC - 7721细胞的生长。

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