Inhibition of cell proliferation through an ATP-responsive co-delivery system of doxorubicin and Bcl-2 siRNA

Jianxu Zhang,1,2,* Yudi Wang,2,* Jiawen Chen,2 Xiao Liang,2 Haobo Han,1,2 Yan Yang,2 Quanshun Li,1,2 Yanbo Wang1 1Department of Urology, First Hospital of Jilin University, 2Key Laboratory for Molecular Enzymology and Engineering of Ministry of Education, School of Life Sciences, Jilin University,...

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Autores principales: Zhang J, Wang Y, Chen J, Liang X, Han H, Yang Y, Li Q
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Publicado: Dove Medical Press 2017
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spelling oai:doaj.org-article:4cee84d2a3524cbe900ae36f6d0681be2021-12-02T00:40:51ZInhibition of cell proliferation through an ATP-responsive co-delivery system of doxorubicin and Bcl-2 siRNA1178-2013https://doaj.org/article/4cee84d2a3524cbe900ae36f6d0681be2017-07-01T00:00:00Zhttps://www.dovepress.com/inhibition-of-cell-proliferation-through-an-atp-responsive-co-delivery-peer-reviewed-article-IJNhttps://doaj.org/toc/1178-2013Jianxu Zhang,1,2,* Yudi Wang,2,* Jiawen Chen,2 Xiao Liang,2 Haobo Han,1,2 Yan Yang,2 Quanshun Li,1,2 Yanbo Wang1 1Department of Urology, First Hospital of Jilin University, 2Key Laboratory for Molecular Enzymology and Engineering of Ministry of Education, School of Life Sciences, Jilin University, Changchun, People’s Republic of China *These authors contributed equally to the work Abstract: Herein, DNA duplex was constructed through the hybridization of adenosine triphosphate (ATP)-responsive aptamer and its cDNA in which GC-rich motif could be used to load doxorubicin (DOX), and then, cationic polymer PEI25K was used as a carrier to simultaneously condense DOX-Duplex and Bcl-2 siRNA to prepare the ternary nanocomplex polyethylenimine (PEI)/DOX-Duplex/siRNA. The ATP concentration gradient between the cytosol and extracellular environment could achieve the stable loading of DOX in duplex and the rapid drug release in an ATP-responsive manner. Using human prostate tumor cell line PC-3 as a model, an obvious induction of cell proliferation could be detected with a cell viability of 53.3%, which was stronger than single cargo delivery, indicating the synergistic effect between these two components. The enhanced anti-proliferative effect of ternary nanocomplex could be attributed to the improved induction of cell apoptosis in a mitochondria-mediated pathway and cell-cycle arrest at the G2 phase. Overall, the ATP-responsive nanocarrier for co-delivering DOX and Bcl-2 siRNA has been demonstrated to be a smart delivery system with favorable anti-proliferative effect, especially for solving the multidrug resistance of tumors. Keywords: ATP response, aptamer, doxorubicin, Bcl-2 siRNA, anti-proliferation, synergistic effectZhang JWang YChen JLiang XHan HYang YLi QWang YDove Medical PressarticleATP responseaptamerdoxorubicinBcl-2 siRNAanti-proliferationsynergistic effectMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol Volume 12, Pp 4721-4732 (2017)
institution DOAJ
collection DOAJ
language EN
topic ATP response
aptamer
doxorubicin
Bcl-2 siRNA
anti-proliferation
synergistic effect
Medicine (General)
R5-920
spellingShingle ATP response
aptamer
doxorubicin
Bcl-2 siRNA
anti-proliferation
synergistic effect
Medicine (General)
R5-920
Zhang J
Wang Y
Chen J
Liang X
Han H
Yang Y
Li Q
Wang Y
Inhibition of cell proliferation through an ATP-responsive co-delivery system of doxorubicin and Bcl-2 siRNA
description Jianxu Zhang,1,2,* Yudi Wang,2,* Jiawen Chen,2 Xiao Liang,2 Haobo Han,1,2 Yan Yang,2 Quanshun Li,1,2 Yanbo Wang1 1Department of Urology, First Hospital of Jilin University, 2Key Laboratory for Molecular Enzymology and Engineering of Ministry of Education, School of Life Sciences, Jilin University, Changchun, People’s Republic of China *These authors contributed equally to the work Abstract: Herein, DNA duplex was constructed through the hybridization of adenosine triphosphate (ATP)-responsive aptamer and its cDNA in which GC-rich motif could be used to load doxorubicin (DOX), and then, cationic polymer PEI25K was used as a carrier to simultaneously condense DOX-Duplex and Bcl-2 siRNA to prepare the ternary nanocomplex polyethylenimine (PEI)/DOX-Duplex/siRNA. The ATP concentration gradient between the cytosol and extracellular environment could achieve the stable loading of DOX in duplex and the rapid drug release in an ATP-responsive manner. Using human prostate tumor cell line PC-3 as a model, an obvious induction of cell proliferation could be detected with a cell viability of 53.3%, which was stronger than single cargo delivery, indicating the synergistic effect between these two components. The enhanced anti-proliferative effect of ternary nanocomplex could be attributed to the improved induction of cell apoptosis in a mitochondria-mediated pathway and cell-cycle arrest at the G2 phase. Overall, the ATP-responsive nanocarrier for co-delivering DOX and Bcl-2 siRNA has been demonstrated to be a smart delivery system with favorable anti-proliferative effect, especially for solving the multidrug resistance of tumors. Keywords: ATP response, aptamer, doxorubicin, Bcl-2 siRNA, anti-proliferation, synergistic effect
format article
author Zhang J
Wang Y
Chen J
Liang X
Han H
Yang Y
Li Q
Wang Y
author_facet Zhang J
Wang Y
Chen J
Liang X
Han H
Yang Y
Li Q
Wang Y
author_sort Zhang J
title Inhibition of cell proliferation through an ATP-responsive co-delivery system of doxorubicin and Bcl-2 siRNA
title_short Inhibition of cell proliferation through an ATP-responsive co-delivery system of doxorubicin and Bcl-2 siRNA
title_full Inhibition of cell proliferation through an ATP-responsive co-delivery system of doxorubicin and Bcl-2 siRNA
title_fullStr Inhibition of cell proliferation through an ATP-responsive co-delivery system of doxorubicin and Bcl-2 siRNA
title_full_unstemmed Inhibition of cell proliferation through an ATP-responsive co-delivery system of doxorubicin and Bcl-2 siRNA
title_sort inhibition of cell proliferation through an atp-responsive co-delivery system of doxorubicin and bcl-2 sirna
publisher Dove Medical Press
publishDate 2017
url https://doaj.org/article/4cee84d2a3524cbe900ae36f6d0681be
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AT chenj inhibitionofcellproliferationthroughanatpresponsivecodeliverysystemofdoxorubicinandbcl2sirna
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