Recombinant adeno-associated virus mediated RNA interference inhibits metastasis of nasopharyngeal cancer cells in vivo and in vitro by suppression of Epstein-Barr virus encoded LMP-1

被引:9
作者
Li, Xiangping
Liu, Xiong
Li, Christine Y. S.
Ding, Yanqing
Chau, David
Li, Gang
Kung, Hsiang-Fu
Lin, Marie C. M.
Peng, Ying [1 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 2, Dept Neurol, Guangzhou 510120, Guangdong, Peoples R China
[2] Nanfang Med Univ, Nanfang Hosp, Dept Otolaryngol, Guangzhou 510515, Guangdong, Peoples R China
[3] Univ Hong Kong, Inst Mol Biol, Hong Kong, Hong Kong, Peoples R China
[4] Univ Hong Kong, Open Lab Chem Biol, Inst Mol Technol Drug Discovery, Hong Kong, Hong Kong, Peoples R China
[5] Chinese Univ Hong Kong, Fac Med, Li Ka Shing Inst Hlth Sci, Hong Kong, Hong Kong, Peoples R China
[6] Chinese Univ Hong Kong, Fac Med, Ctr Emerging Infect Dis, Hong Kong, Hong Kong, Peoples R China
关键词
rAAV; nasopharyngeal carcinoma; RNAi; LMP-1; metastasis;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Nasopharyngeal carcinoma (NPC) is a highly metastatic carcinoma characterized by consistent association with Epstein-Barr virus (EBV). Of the EBV-encoded product, latent membrane protein-1 (LMP-1) is considered to be an oncoprotein playing an essential role in cell transformation and metastasis. In this study, we used a recombinant adeno-associated virus type 2 vector (rAAV-2) to deliver small hairpin RNA (shRNA) targeting EBV LMP-1 into the EBV-positive human NPC C666-1 cells and evaluated the effect of long-term suppression of LMP-1 on NPC growth and metastasis in vivo and in vitro. An NPC metastasis nude mouse model with NPC xenograft transplanted in liver was established. The NPC C666-1 cells infected with rAAV-shRNA-LMP-1 or rAAV-EGFP were inoculated in the livers of nude mice. Formation of liver and lung metastasis was evaluated at day 14 after tumor inoculation. Our results demonstrate that rAAV-shRNA-LMP-1 effectively infected C666-1 cells and suppressed LMP-1 expression. Such suppression, in turn, did not significantly inhibit tumor growth, but prevented NPC metastasis in the liver as well as in the lung. Consistent with in vivo data, the in vitro studies in NPC C666-1 cell cultures showed that suppression of LMP-1 by rAAV-shRNA-LMP-1 significantly reduced cell mobility and transmembrane invasion ability. These results demonstrated for the first time that long-term suppression of EBV-encoded LMP-1 in vivo is an effective means for preventing NPC metastasis.
引用
收藏
页码:595 / 603
页数:9
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