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α(1)-Acid Glycoprotein-Decorated Hyaluronic Acid Nanoparticles for Suppressing Metastasis and Overcoming Drug Resistance Breast Cancer

Robust inflammation-suppressing nanoparticles based on α(1)-acid glycoprotein (AGP)-conjugated hyaluronic acid nanoparticles (AGP-HA NPs) were designed to regulate breast cancer cells’ sensitivity to chemotherapy and to suppress tumor metastasis. The successful conjugation between AGP and HA NPs was...

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Autores principales: Omar, Haneen, Fardous, Roa’, Alhindi, Yasser M., Aodah, Alhassan H., Alyami, Mram, Alsuabeyl, Mohammed S., Alghamdi, Waleed M., Alhasan, Ali H., Almalik, Abdulaziz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8962395/
https://www.ncbi.nlm.nih.gov/pubmed/35203623
http://dx.doi.org/10.3390/biomedicines10020414
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author Omar, Haneen
Fardous, Roa’
Alhindi, Yasser M.
Aodah, Alhassan H.
Alyami, Mram
Alsuabeyl, Mohammed S.
Alghamdi, Waleed M.
Alhasan, Ali H.
Almalik, Abdulaziz
author_facet Omar, Haneen
Fardous, Roa’
Alhindi, Yasser M.
Aodah, Alhassan H.
Alyami, Mram
Alsuabeyl, Mohammed S.
Alghamdi, Waleed M.
Alhasan, Ali H.
Almalik, Abdulaziz
author_sort Omar, Haneen
collection PubMed
description Robust inflammation-suppressing nanoparticles based on α(1)-acid glycoprotein (AGP)-conjugated hyaluronic acid nanoparticles (AGP-HA NPs) were designed to regulate breast cancer cells’ sensitivity to chemotherapy and to suppress tumor metastasis. The successful conjugation between AGP and HA NPs was confirmed using FTIR, zeta potential, and UV–vis spectroscopy. In vitro studies on MCF-7 cells indicated the remarkable ability of AGP-HA NPs in suppressing migratory tumor ability by 79% after 24 h. Moreover, the efficacy study showed the high capability of AGP-HA NPs in modulating MDA-MB-231 cells and restoring cell sensitivity to the chemotherapeutic drug doxorubicin (DOX). Furthermore, the finding obtained by flow cytometry and confocal spectroscopy demonstrated that AGP-HA NPs enhanced DOX uptake/retention and aided it to reach cell nucleus within 4 h of incubation. Therefore, AGP-HA NPs represent a viable and effective treatment option to strengthen the anticancer effects of chemotherapeutic agents and potentially improve patients’ survival rates.
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spelling pubmed-89623952022-03-30 α(1)-Acid Glycoprotein-Decorated Hyaluronic Acid Nanoparticles for Suppressing Metastasis and Overcoming Drug Resistance Breast Cancer Omar, Haneen Fardous, Roa’ Alhindi, Yasser M. Aodah, Alhassan H. Alyami, Mram Alsuabeyl, Mohammed S. Alghamdi, Waleed M. Alhasan, Ali H. Almalik, Abdulaziz Biomedicines Article Robust inflammation-suppressing nanoparticles based on α(1)-acid glycoprotein (AGP)-conjugated hyaluronic acid nanoparticles (AGP-HA NPs) were designed to regulate breast cancer cells’ sensitivity to chemotherapy and to suppress tumor metastasis. The successful conjugation between AGP and HA NPs was confirmed using FTIR, zeta potential, and UV–vis spectroscopy. In vitro studies on MCF-7 cells indicated the remarkable ability of AGP-HA NPs in suppressing migratory tumor ability by 79% after 24 h. Moreover, the efficacy study showed the high capability of AGP-HA NPs in modulating MDA-MB-231 cells and restoring cell sensitivity to the chemotherapeutic drug doxorubicin (DOX). Furthermore, the finding obtained by flow cytometry and confocal spectroscopy demonstrated that AGP-HA NPs enhanced DOX uptake/retention and aided it to reach cell nucleus within 4 h of incubation. Therefore, AGP-HA NPs represent a viable and effective treatment option to strengthen the anticancer effects of chemotherapeutic agents and potentially improve patients’ survival rates. MDPI 2022-02-09 /pmc/articles/PMC8962395/ /pubmed/35203623 http://dx.doi.org/10.3390/biomedicines10020414 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Omar, Haneen
Fardous, Roa’
Alhindi, Yasser M.
Aodah, Alhassan H.
Alyami, Mram
Alsuabeyl, Mohammed S.
Alghamdi, Waleed M.
Alhasan, Ali H.
Almalik, Abdulaziz
α(1)-Acid Glycoprotein-Decorated Hyaluronic Acid Nanoparticles for Suppressing Metastasis and Overcoming Drug Resistance Breast Cancer
title α(1)-Acid Glycoprotein-Decorated Hyaluronic Acid Nanoparticles for Suppressing Metastasis and Overcoming Drug Resistance Breast Cancer
title_full α(1)-Acid Glycoprotein-Decorated Hyaluronic Acid Nanoparticles for Suppressing Metastasis and Overcoming Drug Resistance Breast Cancer
title_fullStr α(1)-Acid Glycoprotein-Decorated Hyaluronic Acid Nanoparticles for Suppressing Metastasis and Overcoming Drug Resistance Breast Cancer
title_full_unstemmed α(1)-Acid Glycoprotein-Decorated Hyaluronic Acid Nanoparticles for Suppressing Metastasis and Overcoming Drug Resistance Breast Cancer
title_short α(1)-Acid Glycoprotein-Decorated Hyaluronic Acid Nanoparticles for Suppressing Metastasis and Overcoming Drug Resistance Breast Cancer
title_sort α(1)-acid glycoprotein-decorated hyaluronic acid nanoparticles for suppressing metastasis and overcoming drug resistance breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8962395/
https://www.ncbi.nlm.nih.gov/pubmed/35203623
http://dx.doi.org/10.3390/biomedicines10020414
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