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RNA interference‐mediated silencing of focal adhesion kinase inhibits growth of human malignant glioma xenograft in nude mice
Author(s) -
Wang GuanJie,
Ma YongPing,
Yang Yang,
Zhang Na,
Wang Wei,
Liu ShengYong,
Chen LiJuan,
Jiang Yu,
Zhao Xia,
Wei YuQuan,
Deng HongXin
Publication year - 2011
Publication title -
cell biology international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.932
H-Index - 77
eISSN - 1095-8355
pISSN - 1065-6995
DOI - 10.1042/cbi20100243
Subject(s) - cationic liposome , small hairpin rna , cancer research , focal adhesion , cell growth , microbiology and biotechnology , angiogenesis , biology , glioma , gene knockdown , transfection , dna laddering , apoptosis , chemistry , cell culture , programmed cell death , signal transduction , biochemistry , genetics , dna fragmentation
FAK (focal adhesion kinase), which plays a pivotal role in mediating cell proliferation, survival and migration, is frequently overexpressed in human malignant glioma. The expression of FAK increases with the advance of tumour grade and stage. Based on these observations, we hypothesized that attenuation of FAK expression may have inhibitory effects on the growth of malignant glioma. In the present study, human glioma cell line U251 was transfected with plasmids containing U6 promoter‐driven shRNAs (small‐hairpin RNAs) against human FAK using cationic liposome. The effects of FAK knockdown in U251 cells in vitro were analysed by using flow cytometry and PI (propidium iodide)‐staining assays. Based on the encouraging in vitro results with FAK silencing, plasmids encoding FAK‐targeted shRNA were encapsulated by DOTAP (dioleoyltrimethylammonium propane): Chol (cholesterol) cationic liposome and injected via tail vein to evaluate its therapeutic efficiency on suppressing tumour growth in a human glioma xenograft model. PCNA (proliferating‐cell nuclear antigen), CD34 immunostaining and TUNEL (terminal deoxynucleotidyl transferase‐mediated dUTP nick‐end labelling) assay were used to assess the changes in tumour angiogenesis, apoptosis and proliferation respectively. The results indicated that DOTAP:Chol cationic liposome could deliver therapeutic plasmids systemically to tumour xenografts, resulting in suppression of tumour growth. Treatment with plasmid encoding FAK‐targeted shRNA reduced mean tumour volume by approx. 70% compared with control groups ( P <0.05), accompanied with angiogenesis inhibition ( P <0.05), tumour cell proliferation suppression ( P <0.05) and apoptosis induction ( P <0.05). Taken together, our results demonstrated that shRNA‐mediated silencing of FAK might be a potential therapeutic approach against human malignant glioma.