Targeting breast cancer stem cells by a self-assembled, aptamer-conjugated DNA nanotrain with preloading doxorubicin

Zhiyuan Xu,1 Ronghua Ni,1 Yun Chen1,21School of Pharmacy, Nanjing Medical University, Nanjing 211166, People’s Republic of China; 2State Key Laboratory of Reproductive Medicine, Nanjing 210029, People’s Republic of ChinaCorrespondence: Yun ChenSchool of Pharmacy, Nanjing Medical...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Xu Z, Ni R, Chen Y
Formato: article
Lenguaje:EN
Publicado: Dove Medical Press 2019
Materias:
Acceso en línea:https://doaj.org/article/9b7e21103242479c8ff792d889d18abf
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:9b7e21103242479c8ff792d889d18abf
record_format dspace
spelling oai:doaj.org-article:9b7e21103242479c8ff792d889d18abf2021-12-02T08:04:49ZTargeting breast cancer stem cells by a self-assembled, aptamer-conjugated DNA nanotrain with preloading doxorubicin1178-2013https://doaj.org/article/9b7e21103242479c8ff792d889d18abf2019-08-01T00:00:00Zhttps://www.dovepress.com/targeting-breast-cancer-stem-cells-by-a-self-assembled-aptamer-conjuga-peer-reviewed-article-IJNhttps://doaj.org/toc/1178-2013Zhiyuan Xu,1 Ronghua Ni,1 Yun Chen1,21School of Pharmacy, Nanjing Medical University, Nanjing 211166, People’s Republic of China; 2State Key Laboratory of Reproductive Medicine, Nanjing 210029, People’s Republic of ChinaCorrespondence: Yun ChenSchool of Pharmacy, Nanjing Medical University, 818 Tian Yuan East Road, Nanjing 211166, People’s Republic of ChinaTel +86 258 686 8326Fax +86 258 686 8467Email ychen@njmu.edu.cnBackground: Cancer relapse and metastasis is an obstacle to the treatment of breast cancer. Breast cancer stem cells (BCSCs), which can evade the killing effect of traditional chemotherapies, such as doxorubicin (DOX), may contribute to cancer development. Therefore, it is necessary to develop novel drugs that can target and eliminate BCSCs. While multiple strategies have been conceived, they are normally limited by the low drug loading capacity.Purpose: An aptamer-conjugated DNA nanotrain TA6NT-AKTin-DOX, which consists of a CD44 aptamer TA6, DNA building blocks M1 and M2 conjugated with an AKT inhibitor peptide AKTin individually and DOX, was designed.Methods: This DNA nanotrain was prepared through hybridization chain reactionand this highly ordered DNA duplex has plenty of sites where DOX and AKTin can be intercalated or anchored. By performing on MCF-7 BCSCs and tumors by xenografting BCSCs into nude mice, efficacy of the newly prepared drug was evaluated and compared with that of free DOX and various DNA nanotrains.Results: TA6NT-AKTin-DOX showed better efficacy both in vitro and in vivo. To some extent, the enhanced efficacy could be attributed to the targeting effect of TA6 and the high drug loading capacity of the nanotrain (∼20 DOX molecules). Besides, a synergistic response was demonstrated by combining DOX with AKTin, probably due to that the anchored AKTin can reverse the drug resistance of BCSCs including apoptosis resistance and ABC transporters overexpression via the AKT signaling pathway.Conclusion: The aptamer-conjugated DNA nanotrain TA6NT-AKTin-DOX demonstrated its targeting capability to BCSCs.Keywords: breast cancer stem cells (BCSCs), aptamer-conjugated DNA nanotrain, CD44 aptamer TA6, doxorubicin (DOX), AKT peptide inhibitor, hybridization chain reactionXu ZNi RChen YDove Medical PressarticleBreast cancer stem cells (BCSCs)Aptamer-conjugated DNA nanotrainCD44 aptamer TA6Doxorubicin (DOX)AKT peptide inhibitorHybridization chain reactionMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol Volume 14, Pp 6831-6842 (2019)
institution DOAJ
collection DOAJ
language EN
topic Breast cancer stem cells (BCSCs)
Aptamer-conjugated DNA nanotrain
CD44 aptamer TA6
Doxorubicin (DOX)
AKT peptide inhibitor
Hybridization chain reaction
Medicine (General)
R5-920
spellingShingle Breast cancer stem cells (BCSCs)
Aptamer-conjugated DNA nanotrain
CD44 aptamer TA6
Doxorubicin (DOX)
AKT peptide inhibitor
Hybridization chain reaction
Medicine (General)
R5-920
Xu Z
Ni R
Chen Y
Targeting breast cancer stem cells by a self-assembled, aptamer-conjugated DNA nanotrain with preloading doxorubicin
description Zhiyuan Xu,1 Ronghua Ni,1 Yun Chen1,21School of Pharmacy, Nanjing Medical University, Nanjing 211166, People’s Republic of China; 2State Key Laboratory of Reproductive Medicine, Nanjing 210029, People’s Republic of ChinaCorrespondence: Yun ChenSchool of Pharmacy, Nanjing Medical University, 818 Tian Yuan East Road, Nanjing 211166, People’s Republic of ChinaTel +86 258 686 8326Fax +86 258 686 8467Email ychen@njmu.edu.cnBackground: Cancer relapse and metastasis is an obstacle to the treatment of breast cancer. Breast cancer stem cells (BCSCs), which can evade the killing effect of traditional chemotherapies, such as doxorubicin (DOX), may contribute to cancer development. Therefore, it is necessary to develop novel drugs that can target and eliminate BCSCs. While multiple strategies have been conceived, they are normally limited by the low drug loading capacity.Purpose: An aptamer-conjugated DNA nanotrain TA6NT-AKTin-DOX, which consists of a CD44 aptamer TA6, DNA building blocks M1 and M2 conjugated with an AKT inhibitor peptide AKTin individually and DOX, was designed.Methods: This DNA nanotrain was prepared through hybridization chain reactionand this highly ordered DNA duplex has plenty of sites where DOX and AKTin can be intercalated or anchored. By performing on MCF-7 BCSCs and tumors by xenografting BCSCs into nude mice, efficacy of the newly prepared drug was evaluated and compared with that of free DOX and various DNA nanotrains.Results: TA6NT-AKTin-DOX showed better efficacy both in vitro and in vivo. To some extent, the enhanced efficacy could be attributed to the targeting effect of TA6 and the high drug loading capacity of the nanotrain (∼20 DOX molecules). Besides, a synergistic response was demonstrated by combining DOX with AKTin, probably due to that the anchored AKTin can reverse the drug resistance of BCSCs including apoptosis resistance and ABC transporters overexpression via the AKT signaling pathway.Conclusion: The aptamer-conjugated DNA nanotrain TA6NT-AKTin-DOX demonstrated its targeting capability to BCSCs.Keywords: breast cancer stem cells (BCSCs), aptamer-conjugated DNA nanotrain, CD44 aptamer TA6, doxorubicin (DOX), AKT peptide inhibitor, hybridization chain reaction
format article
author Xu Z
Ni R
Chen Y
author_facet Xu Z
Ni R
Chen Y
author_sort Xu Z
title Targeting breast cancer stem cells by a self-assembled, aptamer-conjugated DNA nanotrain with preloading doxorubicin
title_short Targeting breast cancer stem cells by a self-assembled, aptamer-conjugated DNA nanotrain with preloading doxorubicin
title_full Targeting breast cancer stem cells by a self-assembled, aptamer-conjugated DNA nanotrain with preloading doxorubicin
title_fullStr Targeting breast cancer stem cells by a self-assembled, aptamer-conjugated DNA nanotrain with preloading doxorubicin
title_full_unstemmed Targeting breast cancer stem cells by a self-assembled, aptamer-conjugated DNA nanotrain with preloading doxorubicin
title_sort targeting breast cancer stem cells by a self-assembled, aptamer-conjugated dna nanotrain with preloading doxorubicin
publisher Dove Medical Press
publishDate 2019
url https://doaj.org/article/9b7e21103242479c8ff792d889d18abf
work_keys_str_mv AT xuz targetingbreastcancerstemcellsbyaselfassembledaptamerconjugateddnananotrainwithpreloadingdoxorubicin
AT nir targetingbreastcancerstemcellsbyaselfassembledaptamerconjugateddnananotrainwithpreloadingdoxorubicin
AT cheny targetingbreastcancerstemcellsbyaselfassembledaptamerconjugateddnananotrainwithpreloadingdoxorubicin
_version_ 1718398675372212224