VEGF siRNA delivered by polycation liposome-encapsulated calcium phosphate nanoparticles for tumor angiogenesis inhibition in breast cancer

被引:53
作者
Chen, Jinliang [1 ]
Sun, Xiaoyi [2 ]
Shao, Rong [1 ]
Xu, Yichao [1 ]
Gao, Jianqing [3 ]
Liang, Wenquan [3 ]
机构
[1] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Ctr Clin Pharmacol, Jiefang Rd 88, Hangzhou 310009, Zhejiang, Peoples R China
[2] Zhejiang Univ City Coll, Dept Pharm, Hangzhou, Zhejiang, Peoples R China
[3] Zhejiang Univ, Coll Pharmaceut Sci, Inst Pharmaceut, Hangzhou, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
polycation liposomes; calcium phosphate nanoparticles; VEGF; siRNA; angiogenesis inhibition; CLINICAL-TRIALS; CO-DELIVERY; TRANSFECTION; THERAPY; RNA; THERAPEUTICS; FORMULATIONS; PACLITAXEL; EFFICIENCY; PHASE;
D O I
10.2147/IJN.S142739
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Angiogenesis plays an important role in tumor development and metastasis, and many cancer cells upregulate VEGF expression to promote angiogenesis. Silencing VEGF expression by RNA interference is expected to be a promising strategy to suppress the tumor growth. However, low transfection efficiency and instability are the main barriers for small interfering RNA (siRNA) delivery. In this study, we developed polycation liposome-encapsulated calcium phosphate nanoparticles (PLCP) for siRNA delivery in vivo. VEGF expression silencing effect in MCF-7 cells was investigated by real-time quantitative polymerase chain reaction and Western blot assay. VEGF siRNA mediated by PLCP can reduce 60%-80% VEGF expression in vitro, which was significantly higher than that mediated by Lipofectamine 2000. Furthermore, significant tumor growth and angiogenesis inhibition were observed in MCF-7 xenografts mice when treated with PLCP/VEGF siRNA or combined with doxorubicin. In conclusion, the combination of silencing VEGF expression and chemotherapeutics would be a potential treatment for cancer therapy.
引用
收藏
页码:6075 / 6088
页数:14
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