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Therapeutic Approaches to Target Cancer Stem Cells

The clinical relevance of cancer stem cells (CSC) remains a major challenge for current cancer therapies, but preliminary findings indicate that specific targeting may be possible. Recent studies have shown that these tumor subpopulations promote tumor angiogenesis through the increased production o...

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Detalles Bibliográficos
Autores principales: Diaz, Arlhee, Leon, Kalet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759198/
https://www.ncbi.nlm.nih.gov/pubmed/24212957
http://dx.doi.org/10.3390/cancers3033331
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author Diaz, Arlhee
Leon, Kalet
author_facet Diaz, Arlhee
Leon, Kalet
author_sort Diaz, Arlhee
collection PubMed
description The clinical relevance of cancer stem cells (CSC) remains a major challenge for current cancer therapies, but preliminary findings indicate that specific targeting may be possible. Recent studies have shown that these tumor subpopulations promote tumor angiogenesis through the increased production of VEGF, whereas the VEGF neutralizing antibody bevacizumab specifically inhibits CSC growth. Moreover, nimotuzumab, a monoclonal antibody against the epidermal growth factor receptor (EGFR) with a potent antiangiogenic activity, has been shown by our group to reduce the frequency of CSC-like subpopulations in mouse models of brain tumors when combined with ionizing radiation. These studies and subsequent reports from other groups support the relevance of approaches based on molecular-targeted therapies to selectively attack CSC. This review discusses the relevance of targeting both the EGFR and angiogenic pathways as valid approaches to this aim. We discuss the relevance of identifying better molecular markers to develop drug screening strategies that selectively target CSC.
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spelling pubmed-37591982013-09-04 Therapeutic Approaches to Target Cancer Stem Cells Diaz, Arlhee Leon, Kalet Cancers (Basel) Review The clinical relevance of cancer stem cells (CSC) remains a major challenge for current cancer therapies, but preliminary findings indicate that specific targeting may be possible. Recent studies have shown that these tumor subpopulations promote tumor angiogenesis through the increased production of VEGF, whereas the VEGF neutralizing antibody bevacizumab specifically inhibits CSC growth. Moreover, nimotuzumab, a monoclonal antibody against the epidermal growth factor receptor (EGFR) with a potent antiangiogenic activity, has been shown by our group to reduce the frequency of CSC-like subpopulations in mouse models of brain tumors when combined with ionizing radiation. These studies and subsequent reports from other groups support the relevance of approaches based on molecular-targeted therapies to selectively attack CSC. This review discusses the relevance of targeting both the EGFR and angiogenic pathways as valid approaches to this aim. We discuss the relevance of identifying better molecular markers to develop drug screening strategies that selectively target CSC. Molecular Diversity Preservation International (MDPI) 2011-08-15 /pmc/articles/PMC3759198/ /pubmed/24212957 http://dx.doi.org/10.3390/cancers3033331 Text en © 2011 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 license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Diaz, Arlhee
Leon, Kalet
Therapeutic Approaches to Target Cancer Stem Cells
title Therapeutic Approaches to Target Cancer Stem Cells
title_full Therapeutic Approaches to Target Cancer Stem Cells
title_fullStr Therapeutic Approaches to Target Cancer Stem Cells
title_full_unstemmed Therapeutic Approaches to Target Cancer Stem Cells
title_short Therapeutic Approaches to Target Cancer Stem Cells
title_sort therapeutic approaches to target cancer stem cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759198/
https://www.ncbi.nlm.nih.gov/pubmed/24212957
http://dx.doi.org/10.3390/cancers3033331
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