Copolymer micelles function as pH-responsive nanocarriers to enhance the cytotoxicity of a HER2 aptamer in HER2-positive breast cancer cells

Yinxing Shen,1,2,* Junqi Zhang,2,* Weiju Hao,1 Tong Wang,1 Jing Liu,2 Youhua Xie,2 Shouhong Xu,1 Honglai Liu1 1State Key Laboratory for Advanced Materials, School of Chemistry and Molecular Engineering, East China University of Science and Technology, 2Department of Medical Microbiology and Parasit...

Full description

Bibliographic Details
Main Authors: Shen Y, Zhang J, Hao W, Wang T, Liu J, Xie Y, Xu S, Liu H
Format: Article
Language:English
Published: Dove Medical Press 2018-01-01
Series:International Journal of Nanomedicine
Subjects:
Online Access:https://www.dovepress.com/copolymer-micelles-function-as-ph-responsive-nanocarriers-to-enhance-t-peer-reviewed-article-IJN
_version_ 1831633708871843840
author Shen Y
Zhang J
Hao W
Wang T
Liu J
Xie Y
Xu S
Liu H
author_facet Shen Y
Zhang J
Hao W
Wang T
Liu J
Xie Y
Xu S
Liu H
author_sort Shen Y
collection DOAJ
description Yinxing Shen,1,2,* Junqi Zhang,2,* Weiju Hao,1 Tong Wang,1 Jing Liu,2 Youhua Xie,2 Shouhong Xu,1 Honglai Liu1 1State Key Laboratory for Advanced Materials, School of Chemistry and Molecular Engineering, East China University of Science and Technology, 2Department of Medical Microbiology and Parasitology, Key Laboratory of Medical Molecular Virology of MOE/MOH, School of Basic Medical Sciences, Fudan University, Shanghai, People’s Republic of China *These authors contributed equally to this work Abstract: Efficient delivery of nucleic acids into target cells is crucial for nucleic acid-based therapies. Various nucleic acid delivery systems have been developed, each with its own advantages and limitations. We previously developed a nanoparticle-based delivery system for small chemical drugs using pH-responsive PEG8-PDPA100-PEG8 polymer micelles as carriers. In this study, we extend the application of these pH-responsive micelle-like nanoparticles (MNPs) to deliver oligonucleotides. We demonstrate that the MNPs efficiently encapsulate and deliver oligonucleotides of different lengths (20–100 nt) into cells. The cargo oligonucleotides are rapidly released at pH 5.0. We prepared MNPs carrying a Texas red-fluorescently labeled anti-human epidermal growth factor receptor 2 (HER2) aptamer (HApt). Compared to free HApt, the HApt-MNPs resulted in significantly better cellular uptake, reduced cell viability, and increased apoptosis in SKBR3 breast cancer cells, which overexpress HER2. Moreover, HApt-MNPs were significantly less cytotoxic to MCF7 breast cancer cells, which express low levels of HER2. After cellular uptake, HApt-MNPs mainly accumulated in lysosomes; inhibition of lysosomal activity using bafilomycin A1 and LysoTracker Red staining confirmed that lysosomal activity and low pH were required for HApt-MNP accumulation and release. Furthermore, HER2 protein expression declined significantly following treatment with HApt-MNPs in SKBR3 cells, indicating that HApt-induced translocation of HER2 to lysosomes exerted a potent cytotoxic effect by altering signaling downstream of HER2. In conclusion, this pH-responsive and lysosome-targeting nanoparticle system can efficiently deliver oligonucleotides to specific target cells and has significant potential for nucleic acid-based cancer therapies. Keywords: pH-responsive micelle-like nanoparticles, nucleic acid delivery, HER2-targeted therapy
first_indexed 2024-12-19T05:40:42Z
format Article
id doaj.art-7df50c2931ce4e6193859e25586a52bc
institution Directory Open Access Journal
issn 1178-2013
language English
last_indexed 2024-12-19T05:40:42Z
publishDate 2018-01-01
publisher Dove Medical Press
record_format Article
series International Journal of Nanomedicine
spelling doaj.art-7df50c2931ce4e6193859e25586a52bc2022-12-21T20:34:01ZengDove Medical PressInternational Journal of Nanomedicine1178-20132018-01-01Volume 1353755336553Copolymer micelles function as pH-responsive nanocarriers to enhance the cytotoxicity of a HER2 aptamer in HER2-positive breast cancer cellsShen YZhang JHao WWang TLiu JXie YXu SLiu HYinxing Shen,1,2,* Junqi Zhang,2,* Weiju Hao,1 Tong Wang,1 Jing Liu,2 Youhua Xie,2 Shouhong Xu,1 Honglai Liu1 1State Key Laboratory for Advanced Materials, School of Chemistry and Molecular Engineering, East China University of Science and Technology, 2Department of Medical Microbiology and Parasitology, Key Laboratory of Medical Molecular Virology of MOE/MOH, School of Basic Medical Sciences, Fudan University, Shanghai, People’s Republic of China *These authors contributed equally to this work Abstract: Efficient delivery of nucleic acids into target cells is crucial for nucleic acid-based therapies. Various nucleic acid delivery systems have been developed, each with its own advantages and limitations. We previously developed a nanoparticle-based delivery system for small chemical drugs using pH-responsive PEG8-PDPA100-PEG8 polymer micelles as carriers. In this study, we extend the application of these pH-responsive micelle-like nanoparticles (MNPs) to deliver oligonucleotides. We demonstrate that the MNPs efficiently encapsulate and deliver oligonucleotides of different lengths (20–100 nt) into cells. The cargo oligonucleotides are rapidly released at pH 5.0. We prepared MNPs carrying a Texas red-fluorescently labeled anti-human epidermal growth factor receptor 2 (HER2) aptamer (HApt). Compared to free HApt, the HApt-MNPs resulted in significantly better cellular uptake, reduced cell viability, and increased apoptosis in SKBR3 breast cancer cells, which overexpress HER2. Moreover, HApt-MNPs were significantly less cytotoxic to MCF7 breast cancer cells, which express low levels of HER2. After cellular uptake, HApt-MNPs mainly accumulated in lysosomes; inhibition of lysosomal activity using bafilomycin A1 and LysoTracker Red staining confirmed that lysosomal activity and low pH were required for HApt-MNP accumulation and release. Furthermore, HER2 protein expression declined significantly following treatment with HApt-MNPs in SKBR3 cells, indicating that HApt-induced translocation of HER2 to lysosomes exerted a potent cytotoxic effect by altering signaling downstream of HER2. In conclusion, this pH-responsive and lysosome-targeting nanoparticle system can efficiently deliver oligonucleotides to specific target cells and has significant potential for nucleic acid-based cancer therapies. Keywords: pH-responsive micelle-like nanoparticles, nucleic acid delivery, HER2-targeted therapyhttps://www.dovepress.com/copolymer-micelles-function-as-ph-responsive-nanocarriers-to-enhance-t-peer-reviewed-article-IJNpH-responsive micelle-like nanoparticlesnucleic acid deliveryHER2 targeted therapy
spellingShingle Shen Y
Zhang J
Hao W
Wang T
Liu J
Xie Y
Xu S
Liu H
Copolymer micelles function as pH-responsive nanocarriers to enhance the cytotoxicity of a HER2 aptamer in HER2-positive breast cancer cells
International Journal of Nanomedicine
pH-responsive micelle-like nanoparticles
nucleic acid delivery
HER2 targeted therapy
title Copolymer micelles function as pH-responsive nanocarriers to enhance the cytotoxicity of a HER2 aptamer in HER2-positive breast cancer cells
title_full Copolymer micelles function as pH-responsive nanocarriers to enhance the cytotoxicity of a HER2 aptamer in HER2-positive breast cancer cells
title_fullStr Copolymer micelles function as pH-responsive nanocarriers to enhance the cytotoxicity of a HER2 aptamer in HER2-positive breast cancer cells
title_full_unstemmed Copolymer micelles function as pH-responsive nanocarriers to enhance the cytotoxicity of a HER2 aptamer in HER2-positive breast cancer cells
title_short Copolymer micelles function as pH-responsive nanocarriers to enhance the cytotoxicity of a HER2 aptamer in HER2-positive breast cancer cells
title_sort copolymer micelles function as ph responsive nanocarriers to enhance the cytotoxicity of a her2 aptamer in her2 positive breast cancer cells
topic pH-responsive micelle-like nanoparticles
nucleic acid delivery
HER2 targeted therapy
url https://www.dovepress.com/copolymer-micelles-function-as-ph-responsive-nanocarriers-to-enhance-t-peer-reviewed-article-IJN
work_keys_str_mv AT sheny copolymermicellesfunctionasphresponsivenanocarrierstoenhancethecytotoxicityofaher2aptamerinher2positivebreastcancercells
AT zhangj copolymermicellesfunctionasphresponsivenanocarrierstoenhancethecytotoxicityofaher2aptamerinher2positivebreastcancercells
AT haow copolymermicellesfunctionasphresponsivenanocarrierstoenhancethecytotoxicityofaher2aptamerinher2positivebreastcancercells
AT wangt copolymermicellesfunctionasphresponsivenanocarrierstoenhancethecytotoxicityofaher2aptamerinher2positivebreastcancercells
AT liuj copolymermicellesfunctionasphresponsivenanocarrierstoenhancethecytotoxicityofaher2aptamerinher2positivebreastcancercells
AT xiey copolymermicellesfunctionasphresponsivenanocarrierstoenhancethecytotoxicityofaher2aptamerinher2positivebreastcancercells
AT xus copolymermicellesfunctionasphresponsivenanocarrierstoenhancethecytotoxicityofaher2aptamerinher2positivebreastcancercells
AT liuh copolymermicellesfunctionasphresponsivenanocarrierstoenhancethecytotoxicityofaher2aptamerinher2positivebreastcancercells