共 34 条
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.
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页码:6075 / 6088
页数:14
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