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Targeted EV to Deliver Chemotherapy to Treat Triple-Negative Breast Cancers
Triple-negative breast cancers (TNBCs) are heterogeneous and metastatic, and targeted therapy is highly needed for TNBC treatment. Recent studies showed that extracellular vesicles (EV) have great potential to deliver therapies to treat cancers. This study aimed to develop and evaluate a natural com...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8781632/ https://www.ncbi.nlm.nih.gov/pubmed/35057042 http://dx.doi.org/10.3390/pharmaceutics14010146 |
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author | Si, Yingnan Chen, Kai Ngo, Hanh Giai Guan, Jia Shiung Totoro, Angela Zhou, Zhuoxin Kim, Seulhee Kim, Taehyun Zhou, Lufang Liu, Xiaoguang |
author_facet | Si, Yingnan Chen, Kai Ngo, Hanh Giai Guan, Jia Shiung Totoro, Angela Zhou, Zhuoxin Kim, Seulhee Kim, Taehyun Zhou, Lufang Liu, Xiaoguang |
author_sort | Si, Yingnan |
collection | PubMed |
description | Triple-negative breast cancers (TNBCs) are heterogeneous and metastatic, and targeted therapy is highly needed for TNBC treatment. Recent studies showed that extracellular vesicles (EV) have great potential to deliver therapies to treat cancers. This study aimed to develop and evaluate a natural compound, verrucarin A (Ver-A), delivered by targeted EV, to treat TNBC. First, the surface expression of epidermal growth factor receptor (EGFR) and CD47 were confirmed with immunohistochemistry (IHC) staining of patient tissue microarray, flow cytometry and Western blotting. EVs were isolated from HEK 293F culture and surface tagged with anti-EGFR/CD47 mAbs to construct mAb-EV. The flow cytometry, confocal imaging and live-animal In Vivo Imaging System (IVIS) demonstrated that mAb-EV could effectively target TNBC and deliver the drug. The drug Ver-A, with dosage-dependent high cytotoxicity to TNBC cells, was packed in mAb-EV. The anti-TNBC efficacy study showed that Ver-A blocked tumor growth in both 4T1 xenografted immunocompetent mouse models and TNBC patient-derived xenograft models with minimal side effects. This study demonstrated that the targeted mAb-EV-Ver-A had great potential to treat TNBCs. |
format | Online Article Text |
id | pubmed-8781632 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87816322022-01-22 Targeted EV to Deliver Chemotherapy to Treat Triple-Negative Breast Cancers Si, Yingnan Chen, Kai Ngo, Hanh Giai Guan, Jia Shiung Totoro, Angela Zhou, Zhuoxin Kim, Seulhee Kim, Taehyun Zhou, Lufang Liu, Xiaoguang Pharmaceutics Article Triple-negative breast cancers (TNBCs) are heterogeneous and metastatic, and targeted therapy is highly needed for TNBC treatment. Recent studies showed that extracellular vesicles (EV) have great potential to deliver therapies to treat cancers. This study aimed to develop and evaluate a natural compound, verrucarin A (Ver-A), delivered by targeted EV, to treat TNBC. First, the surface expression of epidermal growth factor receptor (EGFR) and CD47 were confirmed with immunohistochemistry (IHC) staining of patient tissue microarray, flow cytometry and Western blotting. EVs were isolated from HEK 293F culture and surface tagged with anti-EGFR/CD47 mAbs to construct mAb-EV. The flow cytometry, confocal imaging and live-animal In Vivo Imaging System (IVIS) demonstrated that mAb-EV could effectively target TNBC and deliver the drug. The drug Ver-A, with dosage-dependent high cytotoxicity to TNBC cells, was packed in mAb-EV. The anti-TNBC efficacy study showed that Ver-A blocked tumor growth in both 4T1 xenografted immunocompetent mouse models and TNBC patient-derived xenograft models with minimal side effects. This study demonstrated that the targeted mAb-EV-Ver-A had great potential to treat TNBCs. MDPI 2022-01-07 /pmc/articles/PMC8781632/ /pubmed/35057042 http://dx.doi.org/10.3390/pharmaceutics14010146 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 Si, Yingnan Chen, Kai Ngo, Hanh Giai Guan, Jia Shiung Totoro, Angela Zhou, Zhuoxin Kim, Seulhee Kim, Taehyun Zhou, Lufang Liu, Xiaoguang Targeted EV to Deliver Chemotherapy to Treat Triple-Negative Breast Cancers |
title | Targeted EV to Deliver Chemotherapy to Treat Triple-Negative Breast Cancers |
title_full | Targeted EV to Deliver Chemotherapy to Treat Triple-Negative Breast Cancers |
title_fullStr | Targeted EV to Deliver Chemotherapy to Treat Triple-Negative Breast Cancers |
title_full_unstemmed | Targeted EV to Deliver Chemotherapy to Treat Triple-Negative Breast Cancers |
title_short | Targeted EV to Deliver Chemotherapy to Treat Triple-Negative Breast Cancers |
title_sort | targeted ev to deliver chemotherapy to treat triple-negative breast cancers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8781632/ https://www.ncbi.nlm.nih.gov/pubmed/35057042 http://dx.doi.org/10.3390/pharmaceutics14010146 |
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