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Cancer Stem Cell Markers in Rhabdomyosarcoma in Children

(1) Background: The aim of the present study was to assess the cancer stem cell (CSC) markers CD24, CD44, CD133, and ALDH1A1 in rhabdomyosarcoma (RMS) in children and to define their prognostic role in this group of patients. (2) Methods: The study material was archival tissue specimens collected fr...

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Autores principales: Radzikowska, Joanna, Czarnecka, Anna M., Klepacka, Teresa, Rychłowska-Pruszyńska, Magdalena, Raciborska, Anna, Dembowska-Bagińska, Bożenna, Pronicki, Maciej, Kukwa, Andrzej, Fendler, Wojciech, Smyczyńska, Urszula, Kukwa, Wojciech, Krzeski, Antoni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406733/
https://www.ncbi.nlm.nih.gov/pubmed/36010245
http://dx.doi.org/10.3390/diagnostics12081895
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author Radzikowska, Joanna
Czarnecka, Anna M.
Klepacka, Teresa
Rychłowska-Pruszyńska, Magdalena
Raciborska, Anna
Dembowska-Bagińska, Bożenna
Pronicki, Maciej
Kukwa, Andrzej
Fendler, Wojciech
Smyczyńska, Urszula
Kukwa, Wojciech
Krzeski, Antoni
author_facet Radzikowska, Joanna
Czarnecka, Anna M.
Klepacka, Teresa
Rychłowska-Pruszyńska, Magdalena
Raciborska, Anna
Dembowska-Bagińska, Bożenna
Pronicki, Maciej
Kukwa, Andrzej
Fendler, Wojciech
Smyczyńska, Urszula
Kukwa, Wojciech
Krzeski, Antoni
author_sort Radzikowska, Joanna
collection PubMed
description (1) Background: The aim of the present study was to assess the cancer stem cell (CSC) markers CD24, CD44, CD133, and ALDH1A1 in rhabdomyosarcoma (RMS) in children and to define their prognostic role in this group of patients. (2) Methods: The study material was archival tissue specimens collected from 49 patients under 18 years of age and who had been diagnosed with RMS. Immunohistochemistry (IHC) was used to evaluate the expression of the selected CSC markers in the tumor tissue. Expression was evaluated using a semiquantitative IRS scale based on the one developed by Remmele and Stenger and was correlated with the clinical and pathomorphological parameters of prognostic importance in RMS. (3) Results: Expression of the selected CSC markers CD24, CD44, CD133, and ALDH1A1 was demonstrated in 83.7%, 55.1%, 81.6%, and 100% of the RMS patients, respectively. The expression of all of the assessed CSC markers was statistically significantly higher in the study group versus the control group. No significant correlation was found between the expression of the selected CSC markers and clinical and pathological prognostic factors that were analyzed. The expression of the CSC markers did not have a significant influence on RMS survival rates. (4) Conclusions: The results of the conducted study confirm the expression of selected CSC markers in rhabdomyosarcoma tissue in children. The study did not support the prognostic relevance of the expression of any of the assessed CSC markers. However, further studies are needed to fully understand the relevance of the selected CSC markers in RMS carcinogenesis.
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spelling pubmed-94067332022-08-26 Cancer Stem Cell Markers in Rhabdomyosarcoma in Children Radzikowska, Joanna Czarnecka, Anna M. Klepacka, Teresa Rychłowska-Pruszyńska, Magdalena Raciborska, Anna Dembowska-Bagińska, Bożenna Pronicki, Maciej Kukwa, Andrzej Fendler, Wojciech Smyczyńska, Urszula Kukwa, Wojciech Krzeski, Antoni Diagnostics (Basel) Article (1) Background: The aim of the present study was to assess the cancer stem cell (CSC) markers CD24, CD44, CD133, and ALDH1A1 in rhabdomyosarcoma (RMS) in children and to define their prognostic role in this group of patients. (2) Methods: The study material was archival tissue specimens collected from 49 patients under 18 years of age and who had been diagnosed with RMS. Immunohistochemistry (IHC) was used to evaluate the expression of the selected CSC markers in the tumor tissue. Expression was evaluated using a semiquantitative IRS scale based on the one developed by Remmele and Stenger and was correlated with the clinical and pathomorphological parameters of prognostic importance in RMS. (3) Results: Expression of the selected CSC markers CD24, CD44, CD133, and ALDH1A1 was demonstrated in 83.7%, 55.1%, 81.6%, and 100% of the RMS patients, respectively. The expression of all of the assessed CSC markers was statistically significantly higher in the study group versus the control group. No significant correlation was found between the expression of the selected CSC markers and clinical and pathological prognostic factors that were analyzed. The expression of the CSC markers did not have a significant influence on RMS survival rates. (4) Conclusions: The results of the conducted study confirm the expression of selected CSC markers in rhabdomyosarcoma tissue in children. The study did not support the prognostic relevance of the expression of any of the assessed CSC markers. However, further studies are needed to fully understand the relevance of the selected CSC markers in RMS carcinogenesis. MDPI 2022-08-04 /pmc/articles/PMC9406733/ /pubmed/36010245 http://dx.doi.org/10.3390/diagnostics12081895 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Radzikowska, Joanna
Czarnecka, Anna M.
Klepacka, Teresa
Rychłowska-Pruszyńska, Magdalena
Raciborska, Anna
Dembowska-Bagińska, Bożenna
Pronicki, Maciej
Kukwa, Andrzej
Fendler, Wojciech
Smyczyńska, Urszula
Kukwa, Wojciech
Krzeski, Antoni
Cancer Stem Cell Markers in Rhabdomyosarcoma in Children
title Cancer Stem Cell Markers in Rhabdomyosarcoma in Children
title_full Cancer Stem Cell Markers in Rhabdomyosarcoma in Children
title_fullStr Cancer Stem Cell Markers in Rhabdomyosarcoma in Children
title_full_unstemmed Cancer Stem Cell Markers in Rhabdomyosarcoma in Children
title_short Cancer Stem Cell Markers in Rhabdomyosarcoma in Children
title_sort cancer stem cell markers in rhabdomyosarcoma in children
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406733/
https://www.ncbi.nlm.nih.gov/pubmed/36010245
http://dx.doi.org/10.3390/diagnostics12081895
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