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Suitability of CD133 as a Marker for Cancer Stem Cells in Melanoma

OBJECTIVES: CD133 is considered a cancer stem cell (CSC) marker in various malignancies; however, its role as a biomarker of malignant melanoma remains controversial. The present study was conducted to evaluate the suitability of CD133 surface antigen as a CSC marker in melanoma. METHODS: Human mela...

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Autores principales: Korn, Philippe, Kampmann, Andreas, Spalthoff, Simon, Jehn, Philipp, Tavassol, Frank, Lentge, Fritjof, Gellrich, Nils-Claudius, Zimmerer, Rüdiger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: West Asia Organization for Cancer Prevention 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8408398/
https://www.ncbi.nlm.nih.gov/pubmed/34048190
http://dx.doi.org/10.31557/APJCP.2021.22.5.1591
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author Korn, Philippe
Kampmann, Andreas
Spalthoff, Simon
Jehn, Philipp
Tavassol, Frank
Lentge, Fritjof
Gellrich, Nils-Claudius
Zimmerer, Rüdiger
author_facet Korn, Philippe
Kampmann, Andreas
Spalthoff, Simon
Jehn, Philipp
Tavassol, Frank
Lentge, Fritjof
Gellrich, Nils-Claudius
Zimmerer, Rüdiger
author_sort Korn, Philippe
collection PubMed
description OBJECTIVES: CD133 is considered a cancer stem cell (CSC) marker in various malignancies; however, its role as a biomarker of malignant melanoma remains controversial. The present study was conducted to evaluate the suitability of CD133 surface antigen as a CSC marker in melanoma. METHODS: Human melanoma cells were fractionally separated by magnetic cell separation depending on the CD133 phenotype and transplanted into immunodeficient mice to evaluate their tumorigenic capacity. Furthermore, the time until the development of a palpable tumor and the growth rate were measured, and the final tumor volume was assessed after 8 weeks. The immunohistochemical expression of CD133 in the induced neoplasia was then compared using histomorphometry. RESULTS: Notably, neoplasms were induced in all the groups (n = 48), including in the CD133-negative group. Tumors induced by unsorted cells had the largest volume (p = 0.014) but were detected significantly later in this group (p ≤ 0.001). Interestingly, all explanted tumors expressed CD133, with no significant differences among groups. CONCLUSIONS: In contrast to the results obtained in prior studies, the suitability of CD133 as a CSC marker could not be demonstrated. The current encouraging progress in targeted therapy for malignant melanoma highlights the need to identify more effective targets.
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spelling pubmed-84083982021-09-01 Suitability of CD133 as a Marker for Cancer Stem Cells in Melanoma Korn, Philippe Kampmann, Andreas Spalthoff, Simon Jehn, Philipp Tavassol, Frank Lentge, Fritjof Gellrich, Nils-Claudius Zimmerer, Rüdiger Asian Pac J Cancer Prev Research Article OBJECTIVES: CD133 is considered a cancer stem cell (CSC) marker in various malignancies; however, its role as a biomarker of malignant melanoma remains controversial. The present study was conducted to evaluate the suitability of CD133 surface antigen as a CSC marker in melanoma. METHODS: Human melanoma cells were fractionally separated by magnetic cell separation depending on the CD133 phenotype and transplanted into immunodeficient mice to evaluate their tumorigenic capacity. Furthermore, the time until the development of a palpable tumor and the growth rate were measured, and the final tumor volume was assessed after 8 weeks. The immunohistochemical expression of CD133 in the induced neoplasia was then compared using histomorphometry. RESULTS: Notably, neoplasms were induced in all the groups (n = 48), including in the CD133-negative group. Tumors induced by unsorted cells had the largest volume (p = 0.014) but were detected significantly later in this group (p ≤ 0.001). Interestingly, all explanted tumors expressed CD133, with no significant differences among groups. CONCLUSIONS: In contrast to the results obtained in prior studies, the suitability of CD133 as a CSC marker could not be demonstrated. The current encouraging progress in targeted therapy for malignant melanoma highlights the need to identify more effective targets. West Asia Organization for Cancer Prevention 2021-05 /pmc/articles/PMC8408398/ /pubmed/34048190 http://dx.doi.org/10.31557/APJCP.2021.22.5.1591 Text en https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Korn, Philippe
Kampmann, Andreas
Spalthoff, Simon
Jehn, Philipp
Tavassol, Frank
Lentge, Fritjof
Gellrich, Nils-Claudius
Zimmerer, Rüdiger
Suitability of CD133 as a Marker for Cancer Stem Cells in Melanoma
title Suitability of CD133 as a Marker for Cancer Stem Cells in Melanoma
title_full Suitability of CD133 as a Marker for Cancer Stem Cells in Melanoma
title_fullStr Suitability of CD133 as a Marker for Cancer Stem Cells in Melanoma
title_full_unstemmed Suitability of CD133 as a Marker for Cancer Stem Cells in Melanoma
title_short Suitability of CD133 as a Marker for Cancer Stem Cells in Melanoma
title_sort suitability of cd133 as a marker for cancer stem cells in melanoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8408398/
https://www.ncbi.nlm.nih.gov/pubmed/34048190
http://dx.doi.org/10.31557/APJCP.2021.22.5.1591
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