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Preclinical Assessment of Paclitaxel- and Trastuzumab-Delivering Magnetic Nanoparticles Fe(3)O(4) for Treatment and Imaging of HER2-Positive Breast Cancer
Objective: The purpose of this study was to investigate the anticancer activity and the potential imaging use of the innovative combination of magnetic nanoparticles (MNPs)-Fe(3)O(4), paclitaxel (PTX), and trastuzumab (Herceptin) in HER2-positive breast cancer. Methods: MNPs-Fe(3)O(4) was synthesize...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8581045/ https://www.ncbi.nlm.nih.gov/pubmed/34778301 http://dx.doi.org/10.3389/fmed.2021.738775 |
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author | Guo, Liting Zhang, Hongming Liu, Ping Mi, Tianai Ha, Da Su, Li Huang, Lei Shi, Yan Zhang, Jun |
author_facet | Guo, Liting Zhang, Hongming Liu, Ping Mi, Tianai Ha, Da Su, Li Huang, Lei Shi, Yan Zhang, Jun |
author_sort | Guo, Liting |
collection | PubMed |
description | Objective: The purpose of this study was to investigate the anticancer activity and the potential imaging use of the innovative combination of magnetic nanoparticles (MNPs)-Fe(3)O(4), paclitaxel (PTX), and trastuzumab (Herceptin) in HER2-positive breast cancer. Methods: MNPs-Fe(3)O(4) was synthesized and underwent water phase transfer and hydrophobic molecular loading, and its surface was then coupled with Herceptin mono-antibody. The morphological characteristics of MNPs-Fe(3)O(4) were observed under transmission electron microscopy (TEM). Effects of PTX-Herceptin-MNPs-Fe(3)O(4) on breast cancer cells were evaluated using the 3-(4,5-dimethylthiazol-2-yl)-2,4-diphenyltetrazolium bromide assay and the flow cytometric apoptosis assay. To establish a xenograft model, we injected breast cancer SK-BR-3 cells into the left thighs of nude mice. We measured the effect of PTX-Herceptin-MNPs-Fe(3)O(4) on tumor growth by measuring tumor size and calculating inhibition rate with immunohistochemistry analysis further performed, and analyzed MNPs-Fe(3)O(4) accumulation in tumor lesions using in vivo magnetic resonance imaging and in vivo fluorescence imaging. Results: Most MNPs were in spherical shape of about 10 nm in diameter observed under TEM. PTX-Herceptin-MNPs-Fe(3)O(4) showed greater cytotoxic effects, and induced a higher apoptosis rate of SK-BR-3 cells than all the other groups, with corresponding changes of apoptosis-related proteins. Meanwhile, the in vivo tumor xenograft model showed that tumor inhibition rate in the PTX-Herceptin-MNPs-Fe(3)O(4) group was higher than in the PTX-Herceptin group. Furthermore, PTX-Herceptin-MNPs-Fe(3)O(4) enhanced the T2 imaging contrast enhancement effect on tumors in tumor-bearing mice. Conclusion: The novel PTX-Herceptin-MNPs-Fe(3)O(4) combination may represent a promising alternative breast cancer treatment strategy and may facilitate tumor imaging. |
format | Online Article Text |
id | pubmed-8581045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85810452021-11-12 Preclinical Assessment of Paclitaxel- and Trastuzumab-Delivering Magnetic Nanoparticles Fe(3)O(4) for Treatment and Imaging of HER2-Positive Breast Cancer Guo, Liting Zhang, Hongming Liu, Ping Mi, Tianai Ha, Da Su, Li Huang, Lei Shi, Yan Zhang, Jun Front Med (Lausanne) Medicine Objective: The purpose of this study was to investigate the anticancer activity and the potential imaging use of the innovative combination of magnetic nanoparticles (MNPs)-Fe(3)O(4), paclitaxel (PTX), and trastuzumab (Herceptin) in HER2-positive breast cancer. Methods: MNPs-Fe(3)O(4) was synthesized and underwent water phase transfer and hydrophobic molecular loading, and its surface was then coupled with Herceptin mono-antibody. The morphological characteristics of MNPs-Fe(3)O(4) were observed under transmission electron microscopy (TEM). Effects of PTX-Herceptin-MNPs-Fe(3)O(4) on breast cancer cells were evaluated using the 3-(4,5-dimethylthiazol-2-yl)-2,4-diphenyltetrazolium bromide assay and the flow cytometric apoptosis assay. To establish a xenograft model, we injected breast cancer SK-BR-3 cells into the left thighs of nude mice. We measured the effect of PTX-Herceptin-MNPs-Fe(3)O(4) on tumor growth by measuring tumor size and calculating inhibition rate with immunohistochemistry analysis further performed, and analyzed MNPs-Fe(3)O(4) accumulation in tumor lesions using in vivo magnetic resonance imaging and in vivo fluorescence imaging. Results: Most MNPs were in spherical shape of about 10 nm in diameter observed under TEM. PTX-Herceptin-MNPs-Fe(3)O(4) showed greater cytotoxic effects, and induced a higher apoptosis rate of SK-BR-3 cells than all the other groups, with corresponding changes of apoptosis-related proteins. Meanwhile, the in vivo tumor xenograft model showed that tumor inhibition rate in the PTX-Herceptin-MNPs-Fe(3)O(4) group was higher than in the PTX-Herceptin group. Furthermore, PTX-Herceptin-MNPs-Fe(3)O(4) enhanced the T2 imaging contrast enhancement effect on tumors in tumor-bearing mice. Conclusion: The novel PTX-Herceptin-MNPs-Fe(3)O(4) combination may represent a promising alternative breast cancer treatment strategy and may facilitate tumor imaging. Frontiers Media S.A. 2021-10-28 /pmc/articles/PMC8581045/ /pubmed/34778301 http://dx.doi.org/10.3389/fmed.2021.738775 Text en Copyright © 2021 Guo, Zhang, Liu, Mi, Ha, Su, Huang, Shi and Zhang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Medicine Guo, Liting Zhang, Hongming Liu, Ping Mi, Tianai Ha, Da Su, Li Huang, Lei Shi, Yan Zhang, Jun Preclinical Assessment of Paclitaxel- and Trastuzumab-Delivering Magnetic Nanoparticles Fe(3)O(4) for Treatment and Imaging of HER2-Positive Breast Cancer |
title | Preclinical Assessment of Paclitaxel- and Trastuzumab-Delivering Magnetic Nanoparticles Fe(3)O(4) for Treatment and Imaging of HER2-Positive Breast Cancer |
title_full | Preclinical Assessment of Paclitaxel- and Trastuzumab-Delivering Magnetic Nanoparticles Fe(3)O(4) for Treatment and Imaging of HER2-Positive Breast Cancer |
title_fullStr | Preclinical Assessment of Paclitaxel- and Trastuzumab-Delivering Magnetic Nanoparticles Fe(3)O(4) for Treatment and Imaging of HER2-Positive Breast Cancer |
title_full_unstemmed | Preclinical Assessment of Paclitaxel- and Trastuzumab-Delivering Magnetic Nanoparticles Fe(3)O(4) for Treatment and Imaging of HER2-Positive Breast Cancer |
title_short | Preclinical Assessment of Paclitaxel- and Trastuzumab-Delivering Magnetic Nanoparticles Fe(3)O(4) for Treatment and Imaging of HER2-Positive Breast Cancer |
title_sort | preclinical assessment of paclitaxel- and trastuzumab-delivering magnetic nanoparticles fe(3)o(4) for treatment and imaging of her2-positive breast cancer |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8581045/ https://www.ncbi.nlm.nih.gov/pubmed/34778301 http://dx.doi.org/10.3389/fmed.2021.738775 |
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