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Targeting Tumor Endothelial Cells with Nanoparticles

Because angiogenesis is a major contributor to cancer progression and metastasis, it is an attractive target for cancer therapy. Although a diverse number of small compounds for anti-angiogenic therapy have been developed, severe adverse effects commonly occur, since small compounds can affect not o...

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Detalles Bibliográficos
Autores principales: Sakurai, Yu, Akita, Hidetaka, Harashima, Hideyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6928777/
https://www.ncbi.nlm.nih.gov/pubmed/31756900
http://dx.doi.org/10.3390/ijms20235819
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author Sakurai, Yu
Akita, Hidetaka
Harashima, Hideyoshi
author_facet Sakurai, Yu
Akita, Hidetaka
Harashima, Hideyoshi
author_sort Sakurai, Yu
collection PubMed
description Because angiogenesis is a major contributor to cancer progression and metastasis, it is an attractive target for cancer therapy. Although a diverse number of small compounds for anti-angiogenic therapy have been developed, severe adverse effects commonly occur, since small compounds can affect not only tumor endothelial cells (TECs), but also normal endothelial cells. This low selectivity for TECs has motivated researchers to develop alternate types of drug delivery systems (DDSs). In this review, we summarize the current state of knowledge concerning the delivery of nano DDSs to TECs. Their payloads range from small compounds to nucleic acids. Perspectives regarding new therapeutic targets are also mentioned.
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spelling pubmed-69287772019-12-26 Targeting Tumor Endothelial Cells with Nanoparticles Sakurai, Yu Akita, Hidetaka Harashima, Hideyoshi Int J Mol Sci Review Because angiogenesis is a major contributor to cancer progression and metastasis, it is an attractive target for cancer therapy. Although a diverse number of small compounds for anti-angiogenic therapy have been developed, severe adverse effects commonly occur, since small compounds can affect not only tumor endothelial cells (TECs), but also normal endothelial cells. This low selectivity for TECs has motivated researchers to develop alternate types of drug delivery systems (DDSs). In this review, we summarize the current state of knowledge concerning the delivery of nano DDSs to TECs. Their payloads range from small compounds to nucleic acids. Perspectives regarding new therapeutic targets are also mentioned. MDPI 2019-11-20 /pmc/articles/PMC6928777/ /pubmed/31756900 http://dx.doi.org/10.3390/ijms20235819 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Sakurai, Yu
Akita, Hidetaka
Harashima, Hideyoshi
Targeting Tumor Endothelial Cells with Nanoparticles
title Targeting Tumor Endothelial Cells with Nanoparticles
title_full Targeting Tumor Endothelial Cells with Nanoparticles
title_fullStr Targeting Tumor Endothelial Cells with Nanoparticles
title_full_unstemmed Targeting Tumor Endothelial Cells with Nanoparticles
title_short Targeting Tumor Endothelial Cells with Nanoparticles
title_sort targeting tumor endothelial cells with nanoparticles
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6928777/
https://www.ncbi.nlm.nih.gov/pubmed/31756900
http://dx.doi.org/10.3390/ijms20235819
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