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Enhanced Antitumor Efficacy of Macrophage-Mediated Egg Yolk Lipid-Derived Delivery System Against Breast Cancer

BACKGROUND: Chemotherapy is the primary treatment for most cancers apart from surgery. However, the use of chemotherapeutic drugs is limited by side effects and restricted accumulation in tumors because of unique tumor microenvironments. Macrophages have excellent drug delivery potential owing to th...

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Autores principales: Lv, Yanguan, Jun, Yali, Tang, Zhuang, Li, Xiang, Tao, Mingyue, Zhang, Zhengwei, Liu, Lu, Sun, Su’An, Wang, Qilong, Luo, Chao, Zhang, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7736838/
https://www.ncbi.nlm.nih.gov/pubmed/33335395
http://dx.doi.org/10.2147/IJN.S271310
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author Lv, Yanguan
Jun, Yali
Tang, Zhuang
Li, Xiang
Tao, Mingyue
Zhang, Zhengwei
Liu, Lu
Sun, Su’An
Wang, Qilong
Luo, Chao
Zhang, Li
author_facet Lv, Yanguan
Jun, Yali
Tang, Zhuang
Li, Xiang
Tao, Mingyue
Zhang, Zhengwei
Liu, Lu
Sun, Su’An
Wang, Qilong
Luo, Chao
Zhang, Li
author_sort Lv, Yanguan
collection PubMed
description BACKGROUND: Chemotherapy is the primary treatment for most cancers apart from surgery. However, the use of chemotherapeutic drugs is limited by side effects and restricted accumulation in tumors because of unique tumor microenvironments. Macrophages have excellent drug delivery potential owing to their chemotaxis and can home in on tumors. MATERIALS AND METHODS: We developed an effective drug-delivery system for doxorubicin using macrophages. Doxorubicin-loaded egg yolk lipid-derived nanovectors (EYLNs-Dox) were prepared, EYLNs-Dox-loaded macrophages (Mac/EYLNs-Dox) were developed and their tumor penetration and anti-cancer activity against 4T1 cells were analyzed. The biodistribution and anti-4T1 breast cancer activities were determined using 4T1 subcutaneous and lung metastasis models. RESULTS: EYLNs-Dox was successfully internalized into macrophages without affecting their viability and was less toxic than Dox. Mac/EYLNs-Dox penetrated the 4T1 tumor spheroids more efficiently and was more effective in inhibiting tumors in vitro. Macrophages significantly enhanced the distribution of EYLNs vectors in both inflammatory and tumor sites, playing a more effective role in the inhibition of tumors. CONCLUSION: EYLNs-Dox can be effectively delivered using macrophages and Mac/EYLNs-Dox might be a promising targeted delivery system for breast cancer.
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spelling pubmed-77368382020-12-16 Enhanced Antitumor Efficacy of Macrophage-Mediated Egg Yolk Lipid-Derived Delivery System Against Breast Cancer Lv, Yanguan Jun, Yali Tang, Zhuang Li, Xiang Tao, Mingyue Zhang, Zhengwei Liu, Lu Sun, Su’An Wang, Qilong Luo, Chao Zhang, Li Int J Nanomedicine Original Research BACKGROUND: Chemotherapy is the primary treatment for most cancers apart from surgery. However, the use of chemotherapeutic drugs is limited by side effects and restricted accumulation in tumors because of unique tumor microenvironments. Macrophages have excellent drug delivery potential owing to their chemotaxis and can home in on tumors. MATERIALS AND METHODS: We developed an effective drug-delivery system for doxorubicin using macrophages. Doxorubicin-loaded egg yolk lipid-derived nanovectors (EYLNs-Dox) were prepared, EYLNs-Dox-loaded macrophages (Mac/EYLNs-Dox) were developed and their tumor penetration and anti-cancer activity against 4T1 cells were analyzed. The biodistribution and anti-4T1 breast cancer activities were determined using 4T1 subcutaneous and lung metastasis models. RESULTS: EYLNs-Dox was successfully internalized into macrophages without affecting their viability and was less toxic than Dox. Mac/EYLNs-Dox penetrated the 4T1 tumor spheroids more efficiently and was more effective in inhibiting tumors in vitro. Macrophages significantly enhanced the distribution of EYLNs vectors in both inflammatory and tumor sites, playing a more effective role in the inhibition of tumors. CONCLUSION: EYLNs-Dox can be effectively delivered using macrophages and Mac/EYLNs-Dox might be a promising targeted delivery system for breast cancer. Dove 2020-12-10 /pmc/articles/PMC7736838/ /pubmed/33335395 http://dx.doi.org/10.2147/IJN.S271310 Text en © 2020 Lv et al. http://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/). 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
Lv, Yanguan
Jun, Yali
Tang, Zhuang
Li, Xiang
Tao, Mingyue
Zhang, Zhengwei
Liu, Lu
Sun, Su’An
Wang, Qilong
Luo, Chao
Zhang, Li
Enhanced Antitumor Efficacy of Macrophage-Mediated Egg Yolk Lipid-Derived Delivery System Against Breast Cancer
title Enhanced Antitumor Efficacy of Macrophage-Mediated Egg Yolk Lipid-Derived Delivery System Against Breast Cancer
title_full Enhanced Antitumor Efficacy of Macrophage-Mediated Egg Yolk Lipid-Derived Delivery System Against Breast Cancer
title_fullStr Enhanced Antitumor Efficacy of Macrophage-Mediated Egg Yolk Lipid-Derived Delivery System Against Breast Cancer
title_full_unstemmed Enhanced Antitumor Efficacy of Macrophage-Mediated Egg Yolk Lipid-Derived Delivery System Against Breast Cancer
title_short Enhanced Antitumor Efficacy of Macrophage-Mediated Egg Yolk Lipid-Derived Delivery System Against Breast Cancer
title_sort enhanced antitumor efficacy of macrophage-mediated egg yolk lipid-derived delivery system against breast cancer
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7736838/
https://www.ncbi.nlm.nih.gov/pubmed/33335395
http://dx.doi.org/10.2147/IJN.S271310
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