Cargando…
VEGF siRNA delivered by polycation liposome-encapsulated calcium phosphate nanoparticles for tumor angiogenesis inhibition in breast cancer
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...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5573052/ https://www.ncbi.nlm.nih.gov/pubmed/28860767 http://dx.doi.org/10.2147/IJN.S142739 |
_version_ | 1783259603571572736 |
---|---|
author | Chen, Jinliang Sun, Xiaoyi Shao, Rong Xu, Yichao Gao, Jianqing Liang, Wenquan |
author_facet | Chen, Jinliang Sun, Xiaoyi Shao, Rong Xu, Yichao Gao, Jianqing Liang, Wenquan |
author_sort | Chen, Jinliang |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5573052 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55730522017-08-31 VEGF siRNA delivered by polycation liposome-encapsulated calcium phosphate nanoparticles for tumor angiogenesis inhibition in breast cancer Chen, Jinliang Sun, Xiaoyi Shao, Rong Xu, Yichao Gao, Jianqing Liang, Wenquan Int J Nanomedicine Original Research 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. Dove Medical Press 2017-08-21 /pmc/articles/PMC5573052/ /pubmed/28860767 http://dx.doi.org/10.2147/IJN.S142739 Text en © 2017 Chen et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Chen, Jinliang Sun, Xiaoyi Shao, Rong Xu, Yichao Gao, Jianqing Liang, Wenquan VEGF siRNA delivered by polycation liposome-encapsulated calcium phosphate nanoparticles for tumor angiogenesis inhibition in breast cancer |
title | VEGF siRNA delivered by polycation liposome-encapsulated calcium phosphate nanoparticles for tumor angiogenesis inhibition in breast cancer |
title_full | VEGF siRNA delivered by polycation liposome-encapsulated calcium phosphate nanoparticles for tumor angiogenesis inhibition in breast cancer |
title_fullStr | VEGF siRNA delivered by polycation liposome-encapsulated calcium phosphate nanoparticles for tumor angiogenesis inhibition in breast cancer |
title_full_unstemmed | VEGF siRNA delivered by polycation liposome-encapsulated calcium phosphate nanoparticles for tumor angiogenesis inhibition in breast cancer |
title_short | VEGF siRNA delivered by polycation liposome-encapsulated calcium phosphate nanoparticles for tumor angiogenesis inhibition in breast cancer |
title_sort | vegf sirna delivered by polycation liposome-encapsulated calcium phosphate nanoparticles for tumor angiogenesis inhibition in breast cancer |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5573052/ https://www.ncbi.nlm.nih.gov/pubmed/28860767 http://dx.doi.org/10.2147/IJN.S142739 |
work_keys_str_mv | AT chenjinliang vegfsirnadeliveredbypolycationliposomeencapsulatedcalciumphosphatenanoparticlesfortumorangiogenesisinhibitioninbreastcancer AT sunxiaoyi vegfsirnadeliveredbypolycationliposomeencapsulatedcalciumphosphatenanoparticlesfortumorangiogenesisinhibitioninbreastcancer AT shaorong vegfsirnadeliveredbypolycationliposomeencapsulatedcalciumphosphatenanoparticlesfortumorangiogenesisinhibitioninbreastcancer AT xuyichao vegfsirnadeliveredbypolycationliposomeencapsulatedcalciumphosphatenanoparticlesfortumorangiogenesisinhibitioninbreastcancer AT gaojianqing vegfsirnadeliveredbypolycationliposomeencapsulatedcalciumphosphatenanoparticlesfortumorangiogenesisinhibitioninbreastcancer AT liangwenquan vegfsirnadeliveredbypolycationliposomeencapsulatedcalciumphosphatenanoparticlesfortumorangiogenesisinhibitioninbreastcancer |