Polymer–lipid hybrid anti-HER2 nanoparticles for targeted salinomycin delivery to HER2-positive breast cancer stem cells and cancer cells

Jun Li,1,* Wenqing Xu,2,* Xiaoli Yuan,3,* Huaiwen Chen,3 Hao Song,1,4 Bingquan Wang,5 Jun Han5 1College of Pharmacy, Liaocheng University, Liaocheng, Shandong, 2Railway Police College, Zhengzhou, 3Department of Cadre Health Care, Nanjing General Hospital of Nanjing Military Command, Nanjing, Jiangs...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Li J, Xu WQ, Yuan XL, Chen HW, Song H, Wang BQ, Han J
Formato: article
Lenguaje:EN
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://doaj.org/article/ee288ab9e1644ebf9210f26d70a1942d
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:ee288ab9e1644ebf9210f26d70a1942d
record_format dspace
spelling oai:doaj.org-article:ee288ab9e1644ebf9210f26d70a1942d2021-12-02T00:07:18ZPolymer–lipid hybrid anti-HER2 nanoparticles for targeted salinomycin delivery to HER2-positive breast cancer stem cells and cancer cells1178-2013https://doaj.org/article/ee288ab9e1644ebf9210f26d70a1942d2017-09-01T00:00:00Zhttps://www.dovepress.com/polymer-lipid-hybrid-anti-her2-nanoparticles-for-targeted-salinomycin--peer-reviewed-article-IJNhttps://doaj.org/toc/1178-2013Jun Li,1,* Wenqing Xu,2,* Xiaoli Yuan,3,* Huaiwen Chen,3 Hao Song,1,4 Bingquan Wang,5 Jun Han5 1College of Pharmacy, Liaocheng University, Liaocheng, Shandong, 2Railway Police College, Zhengzhou, 3Department of Cadre Health Care, Nanjing General Hospital of Nanjing Military Command, Nanjing, Jiangsu, 4Centre for Stem Cell & Regenerative Medicine, Liaocheng People’s Hospital, 5Institute of Biopharmaceutical Research, Liaocheng University, Liaocheng, Shandong, China *These authors contributed equally to this work Purpose: Breast cancer stem cells (CSCs) are responsible for the initiation, recurrence, and metastasis of breast cancer. Sufficient evidence has established that breast cancer cells can spontaneously turn into breast CSCs. Thus, it is essential to simultaneously target breast CSCs and cancer cells to maximize the efficacy of breast cancer therapy. HER2 has been found to be overexpressed in both breast CSCs and cancer cells. We developed salinomycin-loaded polymer–lipid hybrid anti-HER2 nanoparticles (Sali-NP-HER2) to target both HER2-positive breast CSCs and cancer cells.Methods: The antitumor activity of Sali-NP-HER2 constructed by conjugating anti-HER2 antibodies to polymer–lipid salinomycin nanoparticles was evaluated in vitro and in vivo.Results: Sali-NP-HER2 efficiently bound to HER2-positive breast CSCs and cancer cells, resulting in enhanced cytotoxic effects compared with non-targeted nanoparticles or salinomycin. In mice bearing breast cancer xenografts, administration of Sali-NP-HER2 exhibited superior efficacy in inhibiting tumor growth. Sali-NP-HER2 reduced the breast tumorsphere formation rate and the proportion of breast CSCs more effectively than non-targeted nanoparticles or salinomycin alone.Conclusion: Sali-NP-HER2 represents a promising approach in treating HER2-positive breast cancer by targeting both breast CSCs and cancer cells. Keywords: nanoparticles, breast cancer, cancer stem cells, salinomycin, HER2Li JXu WQYuan XLChen HWSong HWang BQHan JDove Medical PressarticleNanoparticlesBreast cancerCancer stem cellsSalinomycinHER2Medicine (General)R5-920ENInternational Journal of Nanomedicine, Vol Volume 12, Pp 6909-6921 (2017)
institution DOAJ
collection DOAJ
language EN
topic Nanoparticles
Breast cancer
Cancer stem cells
Salinomycin
HER2
Medicine (General)
R5-920
spellingShingle Nanoparticles
Breast cancer
Cancer stem cells
Salinomycin
HER2
Medicine (General)
R5-920
Li J
Xu WQ
Yuan XL
Chen HW
Song H
Wang BQ
Han J
Polymer–lipid hybrid anti-HER2 nanoparticles for targeted salinomycin delivery to HER2-positive breast cancer stem cells and cancer cells
description Jun Li,1,* Wenqing Xu,2,* Xiaoli Yuan,3,* Huaiwen Chen,3 Hao Song,1,4 Bingquan Wang,5 Jun Han5 1College of Pharmacy, Liaocheng University, Liaocheng, Shandong, 2Railway Police College, Zhengzhou, 3Department of Cadre Health Care, Nanjing General Hospital of Nanjing Military Command, Nanjing, Jiangsu, 4Centre for Stem Cell & Regenerative Medicine, Liaocheng People’s Hospital, 5Institute of Biopharmaceutical Research, Liaocheng University, Liaocheng, Shandong, China *These authors contributed equally to this work Purpose: Breast cancer stem cells (CSCs) are responsible for the initiation, recurrence, and metastasis of breast cancer. Sufficient evidence has established that breast cancer cells can spontaneously turn into breast CSCs. Thus, it is essential to simultaneously target breast CSCs and cancer cells to maximize the efficacy of breast cancer therapy. HER2 has been found to be overexpressed in both breast CSCs and cancer cells. We developed salinomycin-loaded polymer–lipid hybrid anti-HER2 nanoparticles (Sali-NP-HER2) to target both HER2-positive breast CSCs and cancer cells.Methods: The antitumor activity of Sali-NP-HER2 constructed by conjugating anti-HER2 antibodies to polymer–lipid salinomycin nanoparticles was evaluated in vitro and in vivo.Results: Sali-NP-HER2 efficiently bound to HER2-positive breast CSCs and cancer cells, resulting in enhanced cytotoxic effects compared with non-targeted nanoparticles or salinomycin. In mice bearing breast cancer xenografts, administration of Sali-NP-HER2 exhibited superior efficacy in inhibiting tumor growth. Sali-NP-HER2 reduced the breast tumorsphere formation rate and the proportion of breast CSCs more effectively than non-targeted nanoparticles or salinomycin alone.Conclusion: Sali-NP-HER2 represents a promising approach in treating HER2-positive breast cancer by targeting both breast CSCs and cancer cells. Keywords: nanoparticles, breast cancer, cancer stem cells, salinomycin, HER2
format article
author Li J
Xu WQ
Yuan XL
Chen HW
Song H
Wang BQ
Han J
author_facet Li J
Xu WQ
Yuan XL
Chen HW
Song H
Wang BQ
Han J
author_sort Li J
title Polymer–lipid hybrid anti-HER2 nanoparticles for targeted salinomycin delivery to HER2-positive breast cancer stem cells and cancer cells
title_short Polymer–lipid hybrid anti-HER2 nanoparticles for targeted salinomycin delivery to HER2-positive breast cancer stem cells and cancer cells
title_full Polymer–lipid hybrid anti-HER2 nanoparticles for targeted salinomycin delivery to HER2-positive breast cancer stem cells and cancer cells
title_fullStr Polymer–lipid hybrid anti-HER2 nanoparticles for targeted salinomycin delivery to HER2-positive breast cancer stem cells and cancer cells
title_full_unstemmed Polymer–lipid hybrid anti-HER2 nanoparticles for targeted salinomycin delivery to HER2-positive breast cancer stem cells and cancer cells
title_sort polymer–lipid hybrid anti-her2 nanoparticles for targeted salinomycin delivery to her2-positive breast cancer stem cells and cancer cells
publisher Dove Medical Press
publishDate 2017
url https://doaj.org/article/ee288ab9e1644ebf9210f26d70a1942d
work_keys_str_mv AT lij polymerndashlipidhybridantiher2nanoparticlesfortargetedsalinomycindeliverytoher2positivebreastcancerstemcellsandcancercells
AT xuwq polymerndashlipidhybridantiher2nanoparticlesfortargetedsalinomycindeliverytoher2positivebreastcancerstemcellsandcancercells
AT yuanxl polymerndashlipidhybridantiher2nanoparticlesfortargetedsalinomycindeliverytoher2positivebreastcancerstemcellsandcancercells
AT chenhw polymerndashlipidhybridantiher2nanoparticlesfortargetedsalinomycindeliverytoher2positivebreastcancerstemcellsandcancercells
AT songh polymerndashlipidhybridantiher2nanoparticlesfortargetedsalinomycindeliverytoher2positivebreastcancerstemcellsandcancercells
AT wangbq polymerndashlipidhybridantiher2nanoparticlesfortargetedsalinomycindeliverytoher2positivebreastcancerstemcellsandcancercells
AT hanj polymerndashlipidhybridantiher2nanoparticlesfortargetedsalinomycindeliverytoher2positivebreastcancerstemcellsandcancercells
_version_ 1718403960192106496