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Targeting cancer stem cells by using the nanoparticles

Cancer stem cells (CSCs) have been shown to be markedly resistant to conventional cancer treatments such as chemotherapy and radiation therapy. Therefore, therapeutic strategies that selectively target CSCs will ultimately lead to better cancer treatments. Currently, accessible conventional therapeu...

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Autores principales: Hong, In-Sun, Jang, Gyu-Beom, Lee, Hwa-Yong, Nam, Jeong-Seok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4583536/
https://www.ncbi.nlm.nih.gov/pubmed/26425092
http://dx.doi.org/10.2147/IJN.S88310
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author Hong, In-Sun
Jang, Gyu-Beom
Lee, Hwa-Yong
Nam, Jeong-Seok
author_facet Hong, In-Sun
Jang, Gyu-Beom
Lee, Hwa-Yong
Nam, Jeong-Seok
author_sort Hong, In-Sun
collection PubMed
description Cancer stem cells (CSCs) have been shown to be markedly resistant to conventional cancer treatments such as chemotherapy and radiation therapy. Therefore, therapeutic strategies that selectively target CSCs will ultimately lead to better cancer treatments. Currently, accessible conventional therapeutic agents mainly eliminate the bulk tumor but do not eliminate CSCs. Therefore, the discovery and improvement of CSC-targeting therapeutic agents are necessary. Nanoparticles effectively inhibit multiple types of CSCs by targeting specific signaling pathways (Wnt/β-catenin, Notch, transforming growth factor-β, and hedgehog signaling) and/or specific markers (aldehyde dehydrogenases, CD44, CD90, and CD133) critically involved in CSC function and maintenance. In this review article, we summarized a number of findings to provide current information about their therapeutic potential of nanoparticles in various cancer cell types and CSCs.
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spelling pubmed-45835362015-09-30 Targeting cancer stem cells by using the nanoparticles Hong, In-Sun Jang, Gyu-Beom Lee, Hwa-Yong Nam, Jeong-Seok Int J Nanomedicine Review Cancer stem cells (CSCs) have been shown to be markedly resistant to conventional cancer treatments such as chemotherapy and radiation therapy. Therefore, therapeutic strategies that selectively target CSCs will ultimately lead to better cancer treatments. Currently, accessible conventional therapeutic agents mainly eliminate the bulk tumor but do not eliminate CSCs. Therefore, the discovery and improvement of CSC-targeting therapeutic agents are necessary. Nanoparticles effectively inhibit multiple types of CSCs by targeting specific signaling pathways (Wnt/β-catenin, Notch, transforming growth factor-β, and hedgehog signaling) and/or specific markers (aldehyde dehydrogenases, CD44, CD90, and CD133) critically involved in CSC function and maintenance. In this review article, we summarized a number of findings to provide current information about their therapeutic potential of nanoparticles in various cancer cell types and CSCs. Dove Medical Press 2015-09-10 /pmc/articles/PMC4583536/ /pubmed/26425092 http://dx.doi.org/10.2147/IJN.S88310 Text en © 2015 Hong et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Hong, In-Sun
Jang, Gyu-Beom
Lee, Hwa-Yong
Nam, Jeong-Seok
Targeting cancer stem cells by using the nanoparticles
title Targeting cancer stem cells by using the nanoparticles
title_full Targeting cancer stem cells by using the nanoparticles
title_fullStr Targeting cancer stem cells by using the nanoparticles
title_full_unstemmed Targeting cancer stem cells by using the nanoparticles
title_short Targeting cancer stem cells by using the nanoparticles
title_sort targeting cancer stem cells by using the nanoparticles
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4583536/
https://www.ncbi.nlm.nih.gov/pubmed/26425092
http://dx.doi.org/10.2147/IJN.S88310
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