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All-stage targeted therapy for the brain metastasis from triple-negative breast cancer
Brain metastasis is a common and serious complication of breast cancer, which is commonly associated with poor survival and prognosis. In particular, the treatment of brain metastasis from triple-negative breast cancer (BM-TNBC) has to face the distinct therapeutic challenges from tumor heterogeneit...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9939358/ https://www.ncbi.nlm.nih.gov/pubmed/36815053 http://dx.doi.org/10.1016/j.apsb.2022.03.026 |
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author | Luo, Zimiao Wu, Sunyi Zhou, Jianfen Xu, Weixia Xu, Qianzhu Lu, Linwei Xie, Cao Liu, Yu Lu, Weiyue |
author_facet | Luo, Zimiao Wu, Sunyi Zhou, Jianfen Xu, Weixia Xu, Qianzhu Lu, Linwei Xie, Cao Liu, Yu Lu, Weiyue |
author_sort | Luo, Zimiao |
collection | PubMed |
description | Brain metastasis is a common and serious complication of breast cancer, which is commonly associated with poor survival and prognosis. In particular, the treatment of brain metastasis from triple-negative breast cancer (BM-TNBC) has to face the distinct therapeutic challenges from tumor heterogeneity, circulating tumor cells (CTCs), blood–brain barrier (BBB) and blood–tumor barrier (BTB), which is in unmet clinical needs. Herein, combining with the advantages of synthetic and natural targeting moieties, we develop a “Y-shaped” peptide pVAP-decorated platelet-hybrid liposome drug delivery system to address the all-stage targeted drug delivery for the whole progression of BM-TNBC. Inherited from the activated platelet, the hybrid liposomes still retain the native affinity toward CTCs. Further, the peptide-mediated targeting to breast cancer cells and transport across BBB/BTB are demonstrated in vitro and in vivo. The resultant delivery platform significantly improves the drug accumulation both in orthotopic breast tumors and brain metastatic lesions, and eventually exhibits an outperformance in the inhibition of BM-TNBC compared with the free drug. Overall, this work provides a promising prospect for the comprehensive treatment of BM-TNBC, which could be generalized to other cell types or used in imaging platforms in the future. |
format | Online Article Text |
id | pubmed-9939358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-99393582023-02-21 All-stage targeted therapy for the brain metastasis from triple-negative breast cancer Luo, Zimiao Wu, Sunyi Zhou, Jianfen Xu, Weixia Xu, Qianzhu Lu, Linwei Xie, Cao Liu, Yu Lu, Weiyue Acta Pharm Sin B Original Article Brain metastasis is a common and serious complication of breast cancer, which is commonly associated with poor survival and prognosis. In particular, the treatment of brain metastasis from triple-negative breast cancer (BM-TNBC) has to face the distinct therapeutic challenges from tumor heterogeneity, circulating tumor cells (CTCs), blood–brain barrier (BBB) and blood–tumor barrier (BTB), which is in unmet clinical needs. Herein, combining with the advantages of synthetic and natural targeting moieties, we develop a “Y-shaped” peptide pVAP-decorated platelet-hybrid liposome drug delivery system to address the all-stage targeted drug delivery for the whole progression of BM-TNBC. Inherited from the activated platelet, the hybrid liposomes still retain the native affinity toward CTCs. Further, the peptide-mediated targeting to breast cancer cells and transport across BBB/BTB are demonstrated in vitro and in vivo. The resultant delivery platform significantly improves the drug accumulation both in orthotopic breast tumors and brain metastatic lesions, and eventually exhibits an outperformance in the inhibition of BM-TNBC compared with the free drug. Overall, this work provides a promising prospect for the comprehensive treatment of BM-TNBC, which could be generalized to other cell types or used in imaging platforms in the future. Elsevier 2023-01 2022-04-06 /pmc/articles/PMC9939358/ /pubmed/36815053 http://dx.doi.org/10.1016/j.apsb.2022.03.026 Text en © 2022 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Luo, Zimiao Wu, Sunyi Zhou, Jianfen Xu, Weixia Xu, Qianzhu Lu, Linwei Xie, Cao Liu, Yu Lu, Weiyue All-stage targeted therapy for the brain metastasis from triple-negative breast cancer |
title | All-stage targeted therapy for the brain metastasis from triple-negative breast cancer |
title_full | All-stage targeted therapy for the brain metastasis from triple-negative breast cancer |
title_fullStr | All-stage targeted therapy for the brain metastasis from triple-negative breast cancer |
title_full_unstemmed | All-stage targeted therapy for the brain metastasis from triple-negative breast cancer |
title_short | All-stage targeted therapy for the brain metastasis from triple-negative breast cancer |
title_sort | all-stage targeted therapy for the brain metastasis from triple-negative breast cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9939358/ https://www.ncbi.nlm.nih.gov/pubmed/36815053 http://dx.doi.org/10.1016/j.apsb.2022.03.026 |
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