Cargando…
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...
Autores principales: | , , , , , , , , |
---|---|
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 |
_version_ | 1784677792784318464 |
---|---|
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. |
format | Online Article Text |
id | pubmed-8962395 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT omarhaneen a1acidglycoproteindecoratedhyaluronicacidnanoparticlesforsuppressingmetastasisandovercomingdrugresistancebreastcancer AT fardousroa a1acidglycoproteindecoratedhyaluronicacidnanoparticlesforsuppressingmetastasisandovercomingdrugresistancebreastcancer AT alhindiyasserm a1acidglycoproteindecoratedhyaluronicacidnanoparticlesforsuppressingmetastasisandovercomingdrugresistancebreastcancer AT aodahalhassanh a1acidglycoproteindecoratedhyaluronicacidnanoparticlesforsuppressingmetastasisandovercomingdrugresistancebreastcancer AT alyamimram a1acidglycoproteindecoratedhyaluronicacidnanoparticlesforsuppressingmetastasisandovercomingdrugresistancebreastcancer AT alsuabeylmohammeds a1acidglycoproteindecoratedhyaluronicacidnanoparticlesforsuppressingmetastasisandovercomingdrugresistancebreastcancer AT alghamdiwaleedm a1acidglycoproteindecoratedhyaluronicacidnanoparticlesforsuppressingmetastasisandovercomingdrugresistancebreastcancer AT alhasanalih a1acidglycoproteindecoratedhyaluronicacidnanoparticlesforsuppressingmetastasisandovercomingdrugresistancebreastcancer AT almalikabdulaziz a1acidglycoproteindecoratedhyaluronicacidnanoparticlesforsuppressingmetastasisandovercomingdrugresistancebreastcancer |