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Authors Chen J, Sun X, Shao R, Xu Y, Gao J, Liang W
Received 27 May 2017
Accepted for publication 29 July 2017
Published 21 August 2017 Volume 2017:12 Pages 6075—6088
DOI https://doi.org/10.2147/IJN.S142739
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Lakshmi Kiran Chelluri
Peer reviewer comments 3
Editor who approved publication: Dr Linlin Sun
Abstract: 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.
Keywords: polycation
liposomes, calcium phosphate nanoparticles, VEGF, siRNA, angiogenesis
inhibition
