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Promising Nanocarriers for PEDF Gene Targeting Delivery to Cervical Cancer Cells Mediated by the Over-expressing FRα

Cervical cancer presents extremely low PEDF expression which is associated with tumor progression and poor prognosis. In this study, folate receptor α (FRα)-targeted nano-liposomes (FLP) were designed to enhance the anti-tumor effect by targeting delivery of exogenous PEDF gene to cervical cancer ce...

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Autores principales: Yang, Yuhan, He, Lili, Liu, Yongmei, Xia, Shan, Fang, Aiping, Xie, Yafei, Gan, Li, He, Zhiyao, Tan, Xiaoyue, Jiang, Chunling, Tong, Aiping, Song, Xiangrong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5006243/
https://www.ncbi.nlm.nih.gov/pubmed/27576898
http://dx.doi.org/10.1038/srep32427
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author Yang, Yuhan
He, Lili
Liu, Yongmei
Xia, Shan
Fang, Aiping
Xie, Yafei
Gan, Li
He, Zhiyao
Tan, Xiaoyue
Jiang, Chunling
Tong, Aiping
Song, Xiangrong
author_facet Yang, Yuhan
He, Lili
Liu, Yongmei
Xia, Shan
Fang, Aiping
Xie, Yafei
Gan, Li
He, Zhiyao
Tan, Xiaoyue
Jiang, Chunling
Tong, Aiping
Song, Xiangrong
author_sort Yang, Yuhan
collection PubMed
description Cervical cancer presents extremely low PEDF expression which is associated with tumor progression and poor prognosis. In this study, folate receptor α (FRα)-targeted nano-liposomes (FLP) were designed to enhance the anti-tumor effect by targeting delivery of exogenous PEDF gene to cervical cancer cells. The targeting molecule F-PEG-Chol was firstly synthesized by a novel simpler method. FLP encapsulating PEDF gene (FLP/PEDF) with a typical lipid-membrane structure were prepared by a film dispersion method. The transfection experiment found FLP could effectively transfect human cervical cancer cells (HeLa cells). FLP/PEDF significantly inhibited the growth of HeLa cells and human umbilical vein endothelial cells (HUVEC cells) and suppressed adhension, invasion and migration of HeLa cells in vitro. In the abdominal metastatic tumor model of cervical cancer, FLP/PEDF administered by intraperitoneal injection exhibited a superior anti-tumor effect probably due to the up-regulated PEDF. FLP/PEDF could not only sharply reduce the microvessel density but also dramatically inhibit proliferation and markedly induce apoptosis of tumor cells in vivo. Moreover, the preliminary safety investigation revealed that FLP/PEDF had no obvious toxicity. These results clearly showed that FLP were desired carriers for PEDF gene and FLP/PEDF might represent a potential novel strategy for gene therapy of cervical cancer.
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spelling pubmed-50062432016-09-07 Promising Nanocarriers for PEDF Gene Targeting Delivery to Cervical Cancer Cells Mediated by the Over-expressing FRα Yang, Yuhan He, Lili Liu, Yongmei Xia, Shan Fang, Aiping Xie, Yafei Gan, Li He, Zhiyao Tan, Xiaoyue Jiang, Chunling Tong, Aiping Song, Xiangrong Sci Rep Article Cervical cancer presents extremely low PEDF expression which is associated with tumor progression and poor prognosis. In this study, folate receptor α (FRα)-targeted nano-liposomes (FLP) were designed to enhance the anti-tumor effect by targeting delivery of exogenous PEDF gene to cervical cancer cells. The targeting molecule F-PEG-Chol was firstly synthesized by a novel simpler method. FLP encapsulating PEDF gene (FLP/PEDF) with a typical lipid-membrane structure were prepared by a film dispersion method. The transfection experiment found FLP could effectively transfect human cervical cancer cells (HeLa cells). FLP/PEDF significantly inhibited the growth of HeLa cells and human umbilical vein endothelial cells (HUVEC cells) and suppressed adhension, invasion and migration of HeLa cells in vitro. In the abdominal metastatic tumor model of cervical cancer, FLP/PEDF administered by intraperitoneal injection exhibited a superior anti-tumor effect probably due to the up-regulated PEDF. FLP/PEDF could not only sharply reduce the microvessel density but also dramatically inhibit proliferation and markedly induce apoptosis of tumor cells in vivo. Moreover, the preliminary safety investigation revealed that FLP/PEDF had no obvious toxicity. These results clearly showed that FLP were desired carriers for PEDF gene and FLP/PEDF might represent a potential novel strategy for gene therapy of cervical cancer. Nature Publishing Group 2016-08-31 /pmc/articles/PMC5006243/ /pubmed/27576898 http://dx.doi.org/10.1038/srep32427 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Yang, Yuhan
He, Lili
Liu, Yongmei
Xia, Shan
Fang, Aiping
Xie, Yafei
Gan, Li
He, Zhiyao
Tan, Xiaoyue
Jiang, Chunling
Tong, Aiping
Song, Xiangrong
Promising Nanocarriers for PEDF Gene Targeting Delivery to Cervical Cancer Cells Mediated by the Over-expressing FRα
title Promising Nanocarriers for PEDF Gene Targeting Delivery to Cervical Cancer Cells Mediated by the Over-expressing FRα
title_full Promising Nanocarriers for PEDF Gene Targeting Delivery to Cervical Cancer Cells Mediated by the Over-expressing FRα
title_fullStr Promising Nanocarriers for PEDF Gene Targeting Delivery to Cervical Cancer Cells Mediated by the Over-expressing FRα
title_full_unstemmed Promising Nanocarriers for PEDF Gene Targeting Delivery to Cervical Cancer Cells Mediated by the Over-expressing FRα
title_short Promising Nanocarriers for PEDF Gene Targeting Delivery to Cervical Cancer Cells Mediated by the Over-expressing FRα
title_sort promising nanocarriers for pedf gene targeting delivery to cervical cancer cells mediated by the over-expressing frα
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5006243/
https://www.ncbi.nlm.nih.gov/pubmed/27576898
http://dx.doi.org/10.1038/srep32427
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