Brief Reports
Copyright ©2005 Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Feb 7, 2005; 11(5): 756-759
Published online Feb 7, 2005. doi: 10.3748/wjg.v11.i5.756
Knockdown of survivin gene expression by RNAi induces apoptosis in human hepatocellular carcinoma cell line SMMC-7721
Sheng-Quan Cheng, Wen-Liang Wang, Wei Yan, Qing-Long Li, Li Wang, Wen-Yong Wang
Sheng-Quan Cheng, Department of Pediatrics, Xijing Hospital, Fourth Military Medical University, Xi’an 710032, Shaanxi Province, China
Wen-Liang Wang, Wei Yan, Qing-Long Li, Li Wang, Wen-Yong Wang, Department of Pathology, Faculty of Preclinical Medicine, Fourth Military Medical University, Xi’an 710032, Shaanxi Province, China
Author contributions: All authors contributed equally to the work.
Correspondence to: Professor Wen-Liang Wang, Department of Pathology, Faculty of Preclinical Medicine, Fourth Military Medical University, Xi’an 710032, Shaanxi Province, China. wlwang@fmmu.edu.cn
Telephone: +86-29-83374595
Received: April 9, 2004
Revised: April 12, 2004
Accepted: May 9, 2004
Published online: February 7, 2005
Abstract

AIM: To investigate the survivin gene expression in human hepatocellular carcinoma cell line SMMC-7721 and the effects of survivin gene RNA interference (RNAi) on cell apoptosis and biological behaviors of SMMC-7721 cells.

METHODS: Eukaryotic expression vector of survivin gene RNAi and recombinant plasmid pSuppressorNeo-survivin(pSuNeo-SVV), were constructed by ligating into the vector, pSupperssorNeo (pSuNeo) digested with restriction enzymes Xba I and Sal I and the designed double-chain RNAi primers. A cell model of SMMC-7721 after treatment with RNAi was prepared by transfecting SMMC-7721 cells with the lipofectin transfection method. Strept-avidin- biotin-complex (SABC) immunohistochemical staining and RT-PCR were used to detect survivin gene expressions in SMMC-7721 cells. Flow cytometry was used for the cell cycle analysis. Transmission electron microscopy was performed to determine whether RNAi induced cell apoptosis, and the method of measuring the cell growth curve was utilized to study the growth of SMMC-7721 cells before and after treatment with RNAi.

RESULTS: The eukaryotic expression vector of survivin gene RNAi and pSuNeo-SVV, were constructed successfully. The expression level of survivin gene in SMMC-7721 cells was observed. After the treatment of RNAi, the expression of survivin gene in SMMC-7721 cells was almost absent, apoptosis index was increased by 15.6%, and the number of cells was decreased in G2/M phase and the cell growth was inhibited.

CONCLUSION: RNAi can exert a knockdown of survivin gene expression in SMMC-7721 cells, and induce apoptosis and inhibit the growth of carcinoma cells.

Keywords: Hepatocellular carcinoma; Survivin; RNA interference; Apoptosis; Gene expression