Efficient inhibition of ovarian cancer by degradable nanoparticle-delivered survivin T34A gene

Li Luo,1,* Ting Du,1,* Jiumeng Zhang,1 Wei Zhao,2 Hao Cheng,1 Yuping Yang,1 Yujiao Wu,1 Chunmei Wang,1 Ke Men,1 Maling Gou1 1State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University and Collaborative Innovation Center for Biotherapy, 2Department of Thoracic Onco...

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Autores principales: Luo L, Du T, Zhang J, Zhao W, Cheng H, Yang Y, Wu Y, Wang C, Men K, Gou M
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Publicado: Dove Medical Press 2016
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spelling oai:doaj.org-article:fcc138b8e99645f7a663360aecbc855c2021-12-02T02:42:32ZEfficient inhibition of ovarian cancer by degradable nanoparticle-delivered survivin T34A gene1178-2013https://doaj.org/article/fcc138b8e99645f7a663360aecbc855c2016-02-01T00:00:00Zhttps://www.dovepress.com/efficient-inhibition-of-ovarian-cancer-by-degradable-nanoparticle-deli-peer-reviewed-article-IJNhttps://doaj.org/toc/1178-2013Li Luo,1,* Ting Du,1,* Jiumeng Zhang,1 Wei Zhao,2 Hao Cheng,1 Yuping Yang,1 Yujiao Wu,1 Chunmei Wang,1 Ke Men,1 Maling Gou1 1State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University and Collaborative Innovation Center for Biotherapy, 2Department of Thoracic Oncology, Cancer Center, West China Hospital, Medical School, Sichuan University, Chengdu, People’s Republic of China *These authors contributed equally to this work Abstract: Gene therapy has promising applications in ovarian cancer therapy. Blocking the function of the survivin protein could lead to the growth inhibition of cancer cells. Herein, we used degradable heparin–polyethyleneimine (HPEI) nanoparticles to deliver a dominant-negative human survivin T34A (hs-T34A) gene to treat ovarian cancer. HPEI nanoparticles were characterized and were found to have a dynamic diameter of 66±4.5 nm and a zeta potential of 27.1±1.87 mV. The constructed hs-T34A gene expression plasmid could be effectively delivered into SKOV3 ovarian carcinoma cells by HPEI nanoparticles with low cytotoxicity. Intraperitoneal administration of HPEI/hs-T34A complexes could markedly inhibit tumor growth in a mouse xenograft model of SKOV3 human ovarian cancer. Moreover, according to our results, apparent apoptosis of cancer cells was observed both in vitro and in vivo. Taken together, the prepared HPEI/hs-T34A formulation showed potential applications in ovarian cancer gene therapy. Keywords: human survivin T34A, heparin–polyethyleneimine nanoparticles, gene therapy, ovarian cancerLuo LDu TZhang JZhao WCheng HYang YWu YWang CMen KGou MDove Medical PressarticleHuman survivin T34AHeparin-polyethyleneimine nanoparticlesGene therapyOvarian cancerMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol 2016, Iss Issue 1, Pp 501-513 (2016)
institution DOAJ
collection DOAJ
language EN
topic Human survivin T34A
Heparin-polyethyleneimine nanoparticles
Gene therapy
Ovarian cancer
Medicine (General)
R5-920
spellingShingle Human survivin T34A
Heparin-polyethyleneimine nanoparticles
Gene therapy
Ovarian cancer
Medicine (General)
R5-920
Luo L
Du T
Zhang J
Zhao W
Cheng H
Yang Y
Wu Y
Wang C
Men K
Gou M
Efficient inhibition of ovarian cancer by degradable nanoparticle-delivered survivin T34A gene
description Li Luo,1,* Ting Du,1,* Jiumeng Zhang,1 Wei Zhao,2 Hao Cheng,1 Yuping Yang,1 Yujiao Wu,1 Chunmei Wang,1 Ke Men,1 Maling Gou1 1State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University and Collaborative Innovation Center for Biotherapy, 2Department of Thoracic Oncology, Cancer Center, West China Hospital, Medical School, Sichuan University, Chengdu, People’s Republic of China *These authors contributed equally to this work Abstract: Gene therapy has promising applications in ovarian cancer therapy. Blocking the function of the survivin protein could lead to the growth inhibition of cancer cells. Herein, we used degradable heparin–polyethyleneimine (HPEI) nanoparticles to deliver a dominant-negative human survivin T34A (hs-T34A) gene to treat ovarian cancer. HPEI nanoparticles were characterized and were found to have a dynamic diameter of 66±4.5 nm and a zeta potential of 27.1±1.87 mV. The constructed hs-T34A gene expression plasmid could be effectively delivered into SKOV3 ovarian carcinoma cells by HPEI nanoparticles with low cytotoxicity. Intraperitoneal administration of HPEI/hs-T34A complexes could markedly inhibit tumor growth in a mouse xenograft model of SKOV3 human ovarian cancer. Moreover, according to our results, apparent apoptosis of cancer cells was observed both in vitro and in vivo. Taken together, the prepared HPEI/hs-T34A formulation showed potential applications in ovarian cancer gene therapy. Keywords: human survivin T34A, heparin–polyethyleneimine nanoparticles, gene therapy, ovarian cancer
format article
author Luo L
Du T
Zhang J
Zhao W
Cheng H
Yang Y
Wu Y
Wang C
Men K
Gou M
author_facet Luo L
Du T
Zhang J
Zhao W
Cheng H
Yang Y
Wu Y
Wang C
Men K
Gou M
author_sort Luo L
title Efficient inhibition of ovarian cancer by degradable nanoparticle-delivered survivin T34A gene
title_short Efficient inhibition of ovarian cancer by degradable nanoparticle-delivered survivin T34A gene
title_full Efficient inhibition of ovarian cancer by degradable nanoparticle-delivered survivin T34A gene
title_fullStr Efficient inhibition of ovarian cancer by degradable nanoparticle-delivered survivin T34A gene
title_full_unstemmed Efficient inhibition of ovarian cancer by degradable nanoparticle-delivered survivin T34A gene
title_sort efficient inhibition of ovarian cancer by degradable nanoparticle-delivered survivin t34a gene
publisher Dove Medical Press
publishDate 2016
url https://doaj.org/article/fcc138b8e99645f7a663360aecbc855c
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