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Engineered collagen-binding serum albumin as a drug conjugate carrier for cancer therapy
Serum albumin (SA) is used as a carrier to deliver cytotoxic agents to tumors via passive targeting. To further improve SA’s tumor targeting capacity, we sought to develop an approach to retain SA-drug conjugates within tumors through a combination of passive and active targeting. SA was recombinant...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6693903/ https://www.ncbi.nlm.nih.gov/pubmed/31453327 http://dx.doi.org/10.1126/sciadv.aaw6081 |
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author | Sasaki, Koichi Ishihara, Jun Ishihara, Ako Miura, Risako Mansurov, Aslan Fukunaga, Kazuto Hubbell, Jeffrey A. |
author_facet | Sasaki, Koichi Ishihara, Jun Ishihara, Ako Miura, Risako Mansurov, Aslan Fukunaga, Kazuto Hubbell, Jeffrey A. |
author_sort | Sasaki, Koichi |
collection | PubMed |
description | Serum albumin (SA) is used as a carrier to deliver cytotoxic agents to tumors via passive targeting. To further improve SA’s tumor targeting capacity, we sought to develop an approach to retain SA-drug conjugates within tumors through a combination of passive and active targeting. SA was recombinantly fused with a collagen-binding domain (CBD) of von Willebrand factor to bind within the tumor stroma after extravasation due to tumor vascular permeability. Doxorubicin (Dox) was conjugated to the CBD-SA via a pH-sensitive linker. Dox-CBD-SA treatment significantly suppressed tumor growth compared to both Dox-SA and aldoxorubicin treatment in a mouse model of breast cancer. Dox-CBD-SA efficiently stimulated host antitumor immunity, resulting in the complete eradication of MC38 colon carcinoma when used in combination with anti–PD-1 checkpoint inhibitor. Dox-CBD-SA decreased adverse events compared to aldoxorubicin. Thus, engineered CBD-SA could be a versatile and clinically relevant drug conjugate carrier protein for treatment of solid tumors. |
format | Online Article Text |
id | pubmed-6693903 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-66939032019-08-26 Engineered collagen-binding serum albumin as a drug conjugate carrier for cancer therapy Sasaki, Koichi Ishihara, Jun Ishihara, Ako Miura, Risako Mansurov, Aslan Fukunaga, Kazuto Hubbell, Jeffrey A. Sci Adv Research Articles Serum albumin (SA) is used as a carrier to deliver cytotoxic agents to tumors via passive targeting. To further improve SA’s tumor targeting capacity, we sought to develop an approach to retain SA-drug conjugates within tumors through a combination of passive and active targeting. SA was recombinantly fused with a collagen-binding domain (CBD) of von Willebrand factor to bind within the tumor stroma after extravasation due to tumor vascular permeability. Doxorubicin (Dox) was conjugated to the CBD-SA via a pH-sensitive linker. Dox-CBD-SA treatment significantly suppressed tumor growth compared to both Dox-SA and aldoxorubicin treatment in a mouse model of breast cancer. Dox-CBD-SA efficiently stimulated host antitumor immunity, resulting in the complete eradication of MC38 colon carcinoma when used in combination with anti–PD-1 checkpoint inhibitor. Dox-CBD-SA decreased adverse events compared to aldoxorubicin. Thus, engineered CBD-SA could be a versatile and clinically relevant drug conjugate carrier protein for treatment of solid tumors. American Association for the Advancement of Science 2019-08-14 /pmc/articles/PMC6693903/ /pubmed/31453327 http://dx.doi.org/10.1126/sciadv.aaw6081 Text en Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Sasaki, Koichi Ishihara, Jun Ishihara, Ako Miura, Risako Mansurov, Aslan Fukunaga, Kazuto Hubbell, Jeffrey A. Engineered collagen-binding serum albumin as a drug conjugate carrier for cancer therapy |
title | Engineered collagen-binding serum albumin as a drug conjugate carrier for cancer therapy |
title_full | Engineered collagen-binding serum albumin as a drug conjugate carrier for cancer therapy |
title_fullStr | Engineered collagen-binding serum albumin as a drug conjugate carrier for cancer therapy |
title_full_unstemmed | Engineered collagen-binding serum albumin as a drug conjugate carrier for cancer therapy |
title_short | Engineered collagen-binding serum albumin as a drug conjugate carrier for cancer therapy |
title_sort | engineered collagen-binding serum albumin as a drug conjugate carrier for cancer therapy |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6693903/ https://www.ncbi.nlm.nih.gov/pubmed/31453327 http://dx.doi.org/10.1126/sciadv.aaw6081 |
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