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(131)I-Labeled Anti-HER2 Nanobody for Targeted Radionuclide Therapy of HER2-Positive Breast Cancer
PURPOSE: The unique structure of nanobodies is advantageous for the development of radiopharmaceuticals for nuclear medicine. Nanobodies targeted to human epidermal growth factor receptor 2 (HER2) can be used as tools for the imaging and therapy of HER2-overexpressing tumors. In this study, we aimed...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10094415/ https://www.ncbi.nlm.nih.gov/pubmed/37064291 http://dx.doi.org/10.2147/IJN.S399322 |
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author | Zhao, Lingzhou Gong, Jiali Qi, Qinli Liu, Changcun Su, Hongxing Xing, Yan Zhao, Jinhua |
author_facet | Zhao, Lingzhou Gong, Jiali Qi, Qinli Liu, Changcun Su, Hongxing Xing, Yan Zhao, Jinhua |
author_sort | Zhao, Lingzhou |
collection | PubMed |
description | PURPOSE: The unique structure of nanobodies is advantageous for the development of radiopharmaceuticals for nuclear medicine. Nanobodies targeted to human epidermal growth factor receptor 2 (HER2) can be used as tools for the imaging and therapy of HER2-overexpressing tumors. In this study, we aimed to describe the generation of a (131)I-labeled anti-HER2 nanobody as a targeted radionuclide therapy (TRNT) agent for HER2-positive breast cancer. METHODS: The anti-HER2 nanobody NM-02 was labeled with (131)I using the iodogen method, and its radiochemical purity and stability in vitro were assessed. The pharmacokinetic profile of (131)I-NM-02 was investigated in normal mice. Tumor accumulation, biodistribution, and therapeutic potential of (131)I-NM-02 were evaluated in HER2-positive SKBR3 xenografts; HER2-negative MB-MDA-231 xenografts were used as the control group. RESULTS: (131)I-NM-02 could be readily prepared with satisfactory radiochemical purity and stability in vitro. Apparent tumor uptake was observed in HER2-positive tumor-bearing mice with rapid blood clearance and favorable biodistribution. (131)I-NM-02 could significantly inhibit tumor growth and extend the life of these mice with good organ compatibility. Negligible tumor accumulation and inhibitory effects of (131)I-NM-02 were observed in the negative control group. CONCLUSION: (131)I-NM-02 has the potential to be explored as a novel tool for TRNT of HER2-positive breast cancer. |
format | Online Article Text |
id | pubmed-10094415 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-100944152023-04-13 (131)I-Labeled Anti-HER2 Nanobody for Targeted Radionuclide Therapy of HER2-Positive Breast Cancer Zhao, Lingzhou Gong, Jiali Qi, Qinli Liu, Changcun Su, Hongxing Xing, Yan Zhao, Jinhua Int J Nanomedicine Original Research PURPOSE: The unique structure of nanobodies is advantageous for the development of radiopharmaceuticals for nuclear medicine. Nanobodies targeted to human epidermal growth factor receptor 2 (HER2) can be used as tools for the imaging and therapy of HER2-overexpressing tumors. In this study, we aimed to describe the generation of a (131)I-labeled anti-HER2 nanobody as a targeted radionuclide therapy (TRNT) agent for HER2-positive breast cancer. METHODS: The anti-HER2 nanobody NM-02 was labeled with (131)I using the iodogen method, and its radiochemical purity and stability in vitro were assessed. The pharmacokinetic profile of (131)I-NM-02 was investigated in normal mice. Tumor accumulation, biodistribution, and therapeutic potential of (131)I-NM-02 were evaluated in HER2-positive SKBR3 xenografts; HER2-negative MB-MDA-231 xenografts were used as the control group. RESULTS: (131)I-NM-02 could be readily prepared with satisfactory radiochemical purity and stability in vitro. Apparent tumor uptake was observed in HER2-positive tumor-bearing mice with rapid blood clearance and favorable biodistribution. (131)I-NM-02 could significantly inhibit tumor growth and extend the life of these mice with good organ compatibility. Negligible tumor accumulation and inhibitory effects of (131)I-NM-02 were observed in the negative control group. CONCLUSION: (131)I-NM-02 has the potential to be explored as a novel tool for TRNT of HER2-positive breast cancer. Dove 2023-04-08 /pmc/articles/PMC10094415/ /pubmed/37064291 http://dx.doi.org/10.2147/IJN.S399322 Text en © 2023 Zhao et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Zhao, Lingzhou Gong, Jiali Qi, Qinli Liu, Changcun Su, Hongxing Xing, Yan Zhao, Jinhua (131)I-Labeled Anti-HER2 Nanobody for Targeted Radionuclide Therapy of HER2-Positive Breast Cancer |
title | (131)I-Labeled Anti-HER2 Nanobody for Targeted Radionuclide Therapy of HER2-Positive Breast Cancer |
title_full | (131)I-Labeled Anti-HER2 Nanobody for Targeted Radionuclide Therapy of HER2-Positive Breast Cancer |
title_fullStr | (131)I-Labeled Anti-HER2 Nanobody for Targeted Radionuclide Therapy of HER2-Positive Breast Cancer |
title_full_unstemmed | (131)I-Labeled Anti-HER2 Nanobody for Targeted Radionuclide Therapy of HER2-Positive Breast Cancer |
title_short | (131)I-Labeled Anti-HER2 Nanobody for Targeted Radionuclide Therapy of HER2-Positive Breast Cancer |
title_sort | (131)i-labeled anti-her2 nanobody for targeted radionuclide therapy of her2-positive breast cancer |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10094415/ https://www.ncbi.nlm.nih.gov/pubmed/37064291 http://dx.doi.org/10.2147/IJN.S399322 |
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