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Molecularly engineered truncated tissue factor with therapeutic aptamers for tumor-targeted delivery and vascular infarction
Selective occlusion of tumor vasculature has proven to be an effective strategy for cancer therapy. Among vascular coagulation agents, the extracellular domain of coagulation-inducing protein tissue factor, truncated tissue factor (tTF), is the most widely used. Since the truncated protein exhibits...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8343113/ https://www.ncbi.nlm.nih.gov/pubmed/34386338 http://dx.doi.org/10.1016/j.apsb.2020.11.014 |
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author | Li, Bozhao Wei, Jingyan Di, Chunzhi Lu, Zefang Qi, Feilong Zhang, Yinlong Leong, Wei Sun Li, Lele Nie, Guangjun Li, Suping |
author_facet | Li, Bozhao Wei, Jingyan Di, Chunzhi Lu, Zefang Qi, Feilong Zhang, Yinlong Leong, Wei Sun Li, Lele Nie, Guangjun Li, Suping |
author_sort | Li, Bozhao |
collection | PubMed |
description | Selective occlusion of tumor vasculature has proven to be an effective strategy for cancer therapy. Among vascular coagulation agents, the extracellular domain of coagulation-inducing protein tissue factor, truncated tissue factor (tTF), is the most widely used. Since the truncated protein exhibits no coagulation activity and is rapidly cleared in the circulation, free tTF cannot be used for cancer treatment on its own but must be combined with other moieties. We here developed a novel, tumor-specific tTF delivery system through coupling tTF with the DNA aptamer, AS1411, which selectively binds to nucleolin receptors overexpressing on the surface of tumor vascular endothelial cells and is specifically cytotoxic to target cells. Systemic administration of the tTF-AS1411 conjugates into tumor-bearing animals induced intravascular thrombosis solely in tumors, thus reducing tumor blood supply and inducing tumor necrosis without apparent side effects. This conjugate represents a uniquely attractive candidate for the clinical translation of vessel occlusion agent for cancer therapy. |
format | Online Article Text |
id | pubmed-8343113 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-83431132021-08-11 Molecularly engineered truncated tissue factor with therapeutic aptamers for tumor-targeted delivery and vascular infarction Li, Bozhao Wei, Jingyan Di, Chunzhi Lu, Zefang Qi, Feilong Zhang, Yinlong Leong, Wei Sun Li, Lele Nie, Guangjun Li, Suping Acta Pharm Sin B Original Article Selective occlusion of tumor vasculature has proven to be an effective strategy for cancer therapy. Among vascular coagulation agents, the extracellular domain of coagulation-inducing protein tissue factor, truncated tissue factor (tTF), is the most widely used. Since the truncated protein exhibits no coagulation activity and is rapidly cleared in the circulation, free tTF cannot be used for cancer treatment on its own but must be combined with other moieties. We here developed a novel, tumor-specific tTF delivery system through coupling tTF with the DNA aptamer, AS1411, which selectively binds to nucleolin receptors overexpressing on the surface of tumor vascular endothelial cells and is specifically cytotoxic to target cells. Systemic administration of the tTF-AS1411 conjugates into tumor-bearing animals induced intravascular thrombosis solely in tumors, thus reducing tumor blood supply and inducing tumor necrosis without apparent side effects. This conjugate represents a uniquely attractive candidate for the clinical translation of vessel occlusion agent for cancer therapy. Elsevier 2021-07 2020-11-24 /pmc/articles/PMC8343113/ /pubmed/34386338 http://dx.doi.org/10.1016/j.apsb.2020.11.014 Text en © 2021 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 Li, Bozhao Wei, Jingyan Di, Chunzhi Lu, Zefang Qi, Feilong Zhang, Yinlong Leong, Wei Sun Li, Lele Nie, Guangjun Li, Suping Molecularly engineered truncated tissue factor with therapeutic aptamers for tumor-targeted delivery and vascular infarction |
title | Molecularly engineered truncated tissue factor with therapeutic aptamers for tumor-targeted delivery and vascular infarction |
title_full | Molecularly engineered truncated tissue factor with therapeutic aptamers for tumor-targeted delivery and vascular infarction |
title_fullStr | Molecularly engineered truncated tissue factor with therapeutic aptamers for tumor-targeted delivery and vascular infarction |
title_full_unstemmed | Molecularly engineered truncated tissue factor with therapeutic aptamers for tumor-targeted delivery and vascular infarction |
title_short | Molecularly engineered truncated tissue factor with therapeutic aptamers for tumor-targeted delivery and vascular infarction |
title_sort | molecularly engineered truncated tissue factor with therapeutic aptamers for tumor-targeted delivery and vascular infarction |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8343113/ https://www.ncbi.nlm.nih.gov/pubmed/34386338 http://dx.doi.org/10.1016/j.apsb.2020.11.014 |
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