RNA interference silences the human papillomavirus 6b/11 early gene E7 in vitro and in vivo

X. Z. Chen(Zhejiang University), Kejian Zhu(Sir Run Run Shaw Hospital), Yi Xu(Sir Run Run Shaw Hospital), Xiaoyun Tang(Sir Run Run Shaw Hospital), Xiaojun Cai(Second Affiliated Hospital of Zhejiang University), X. Zhang(Sir Run Run Shaw Hospital), Hongqiang Cheng(Sir Run Run Shaw Hospital)
Clinical and Experimental Dermatology
October 23, 2009
Cited by 11

Abstract

BACKGROUND: RNA interference (RNAi) is a potential therapeutic tool in the treatment of various diseases, such as cancers and viral infections. Silencing of E7 genes is an effective method to suppress human papilloma virus (HPV)-related tumours. AIM: To determine the therapeutic potential of RNAi in controlling condyloma acuminatum (CA). METHODS: Small interfering (si)RNA duplexes or small-hairpin (sh)RNA-expressing plasmids targeting the E7 genes of HPV-6b or HPV-11were inoculated into cultured E7-expressing cells via cationic liposomes, or into E7 gene-expressing mouse tumour models intratumorally or intravenously. Experiments were performed in triplicate and E7 mRNA level was analysed by real-time PCR. RESULTS: The in vitro experiments found that both siRNAs and shRNA-expressing plasmids reduced the mRNA levels of HPV-6b or HPV-11 E7 to 20-40% at the optimum dosage of 25-50 nmol/L for siRNAs and 0.1-0.2 microg/mL for shRNA-expressing vectors. The optimum time for this to happen was 72 h. E7 mRNA expression in tumour models was reduced to 45-50% after three intratumural injections. Intratumoral injections of RNAi effectors induced greater inhibition than did intravenous injections. CONCLUSIONS: We conclude that HPV-6b/11 E7 gene expression can be specifically modulated by RNAi, which may provide a useful method in the management of CA.


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