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Biomaterials-Mediated Tumor Infarction Therapy

Agents for tumor vascular infarction are recently developed therapeutic agents for the vascular destruction of tumors. They can suppress the progression of the tumor by preventing the flow of nutrition and oxygen to its tissues. Agents of tumor vascular infarction can be divided into three categorie...

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Detalles Bibliográficos
Autores principales: Tong, Shizheng, Zhao, Wei, Zhao, Duoyi, Zhang, Weilin, Zhang, Zhiyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218593/
https://www.ncbi.nlm.nih.gov/pubmed/35757801
http://dx.doi.org/10.3389/fbioe.2022.916926
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author Tong, Shizheng
Zhao, Wei
Zhao, Duoyi
Zhang, Weilin
Zhang, Zhiyu
author_facet Tong, Shizheng
Zhao, Wei
Zhao, Duoyi
Zhang, Weilin
Zhang, Zhiyu
author_sort Tong, Shizheng
collection PubMed
description Agents for tumor vascular infarction are recently developed therapeutic agents for the vascular destruction of tumors. They can suppress the progression of the tumor by preventing the flow of nutrition and oxygen to its tissues. Agents of tumor vascular infarction can be divided into three categories according to the differences in their pathways of action: those that use the thrombin-activating pathway, fibrin-activating pathway, and platelet-activating pathway. However, poor targeting ability, low permeation, and potential side-effects restrict the development of the corresponding drugs. Biomaterials can subtly avoid these drawbacks to suppress the tumor. In this article, the authors summarize currently used biomaterials for tumor infarction therapy with the goal of identifying its mechanism, and discuss outstanding deficiencies in methods of this kind.
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spelling pubmed-92185932022-06-24 Biomaterials-Mediated Tumor Infarction Therapy Tong, Shizheng Zhao, Wei Zhao, Duoyi Zhang, Weilin Zhang, Zhiyu Front Bioeng Biotechnol Bioengineering and Biotechnology Agents for tumor vascular infarction are recently developed therapeutic agents for the vascular destruction of tumors. They can suppress the progression of the tumor by preventing the flow of nutrition and oxygen to its tissues. Agents of tumor vascular infarction can be divided into three categories according to the differences in their pathways of action: those that use the thrombin-activating pathway, fibrin-activating pathway, and platelet-activating pathway. However, poor targeting ability, low permeation, and potential side-effects restrict the development of the corresponding drugs. Biomaterials can subtly avoid these drawbacks to suppress the tumor. In this article, the authors summarize currently used biomaterials for tumor infarction therapy with the goal of identifying its mechanism, and discuss outstanding deficiencies in methods of this kind. Frontiers Media S.A. 2022-06-09 /pmc/articles/PMC9218593/ /pubmed/35757801 http://dx.doi.org/10.3389/fbioe.2022.916926 Text en Copyright © 2022 Tong, Zhao, Zhao, Zhang and Zhang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Tong, Shizheng
Zhao, Wei
Zhao, Duoyi
Zhang, Weilin
Zhang, Zhiyu
Biomaterials-Mediated Tumor Infarction Therapy
title Biomaterials-Mediated Tumor Infarction Therapy
title_full Biomaterials-Mediated Tumor Infarction Therapy
title_fullStr Biomaterials-Mediated Tumor Infarction Therapy
title_full_unstemmed Biomaterials-Mediated Tumor Infarction Therapy
title_short Biomaterials-Mediated Tumor Infarction Therapy
title_sort biomaterials-mediated tumor infarction therapy
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218593/
https://www.ncbi.nlm.nih.gov/pubmed/35757801
http://dx.doi.org/10.3389/fbioe.2022.916926
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