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Molecular identification and targeting of colorectal cancer stem cells

Tumor initiating or cancer stem cells (CSCs) are suggested to be responsible for tumor initiation and growth. Moreover, therapy resistance and minimal residual disease are thought to result from selective resistance of CSCs. Isolation of CSCs from colon carcinomas can be accomplished by selection of...

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Detalles Bibliográficos
Autores principales: Kemper, Kristel, Grandela, Catarina, Medema, Jan Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3248116/
https://www.ncbi.nlm.nih.gov/pubmed/21311095
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author Kemper, Kristel
Grandela, Catarina
Medema, Jan Paul
author_facet Kemper, Kristel
Grandela, Catarina
Medema, Jan Paul
author_sort Kemper, Kristel
collection PubMed
description Tumor initiating or cancer stem cells (CSCs) are suggested to be responsible for tumor initiation and growth. Moreover, therapy resistance and minimal residual disease are thought to result from selective resistance of CSCs. Isolation of CSCs from colon carcinomas can be accomplished by selection of a subpopulation of tumor cells based on expression of one or multiple cell surface markers associated with cancer stemness, like CD133, CD44, CD24, CD29, CD166 and Lgr5. Identification of colon CSCs will lead to a better rational for new therapies that aim to target this fraction specifically. In this review, we analyze known markers used for selection of colon CSCs and their potential function in CSC biology. Moreover, we discuss potential targeting strategies for eradicating CSCs specifically in order to develop more effective therapeutic strategies as well as to address more fundamental questions like the actual role of CSCs in tumor growth.
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spelling pubmed-32481162012-01-18 Molecular identification and targeting of colorectal cancer stem cells Kemper, Kristel Grandela, Catarina Medema, Jan Paul Oncotarget Reviews Tumor initiating or cancer stem cells (CSCs) are suggested to be responsible for tumor initiation and growth. Moreover, therapy resistance and minimal residual disease are thought to result from selective resistance of CSCs. Isolation of CSCs from colon carcinomas can be accomplished by selection of a subpopulation of tumor cells based on expression of one or multiple cell surface markers associated with cancer stemness, like CD133, CD44, CD24, CD29, CD166 and Lgr5. Identification of colon CSCs will lead to a better rational for new therapies that aim to target this fraction specifically. In this review, we analyze known markers used for selection of colon CSCs and their potential function in CSC biology. Moreover, we discuss potential targeting strategies for eradicating CSCs specifically in order to develop more effective therapeutic strategies as well as to address more fundamental questions like the actual role of CSCs in tumor growth. Impact Journals LLC 2010-10-09 /pmc/articles/PMC3248116/ /pubmed/21311095 Text en Copyright: © 2010 Kemper et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
spellingShingle Reviews
Kemper, Kristel
Grandela, Catarina
Medema, Jan Paul
Molecular identification and targeting of colorectal cancer stem cells
title Molecular identification and targeting of colorectal cancer stem cells
title_full Molecular identification and targeting of colorectal cancer stem cells
title_fullStr Molecular identification and targeting of colorectal cancer stem cells
title_full_unstemmed Molecular identification and targeting of colorectal cancer stem cells
title_short Molecular identification and targeting of colorectal cancer stem cells
title_sort molecular identification and targeting of colorectal cancer stem cells
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3248116/
https://www.ncbi.nlm.nih.gov/pubmed/21311095
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