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Functional significance of CD105-positive cells in papillary renal cell carcinoma

BACKGROUND: CD105 was postulated as a renal cell carcinoma (RCC) stem cell marker, and CD133 as a putative RCC progenitor. Hypoxia, a natural microenvironment that prevails in tumors, was also incorporated into the study, especially in terms of the promotion of hypothetical stem-like cell properties...

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Autores principales: Matak, Damian, Brodaczewska, Klaudia K., Szczylik, Cezary, Koch, Irena, Myszczyszyn, Adam, Lipiec, Monika, Lewicki, Slawomir, Szymanski, Lukasz, Zdanowski, Robert, Czarnecka, Anna M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5217207/
https://www.ncbi.nlm.nih.gov/pubmed/28056882
http://dx.doi.org/10.1186/s12885-016-2985-7
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author Matak, Damian
Brodaczewska, Klaudia K.
Szczylik, Cezary
Koch, Irena
Myszczyszyn, Adam
Lipiec, Monika
Lewicki, Slawomir
Szymanski, Lukasz
Zdanowski, Robert
Czarnecka, Anna M.
author_facet Matak, Damian
Brodaczewska, Klaudia K.
Szczylik, Cezary
Koch, Irena
Myszczyszyn, Adam
Lipiec, Monika
Lewicki, Slawomir
Szymanski, Lukasz
Zdanowski, Robert
Czarnecka, Anna M.
author_sort Matak, Damian
collection PubMed
description BACKGROUND: CD105 was postulated as a renal cell carcinoma (RCC) stem cell marker, and CD133 as a putative RCC progenitor. Hypoxia, a natural microenvironment that prevails in tumors, was also incorporated into the study, especially in terms of the promotion of hypothetical stem-like cell properties. METHODS: Within this study, we verify the existence of CD105+ and CD133+ populations in selected papillary subtype RCC (pRCC) cell lines. Both populations were analyzed for correlation with stem-like cell properties, such as stemness gene expression, and sphere and colony formation. For the preliminary analysis, several RCC cell lines were chosen (786-O, SMKT-R2, Caki-2, 796-P, ACHN, RCC6) and the control was human kidney cancer stem cells (HKCSC) and renal cells of embryonic origin (ASE-5063). Four cell lines were chosen for further investigation: Caki-2 (one of the highest numbers of CD105+ cells; primary origin), ACHN (a low number of CD105+ cells; metastatic origin), HKCSC (putative positive control), and ASE-5063 (additional control). RESULTS: In 769-P and RCC6, we could not detect a CD105+ population. Hypoxia variously affects pRCC cell growth, and mainly diminishes the stem-like properties of cells. Furthermore, we could not observe the correlation of CD105 and/or CD133 expression with the enhancement of stem-like properties. CONCLUSIONS: Based on this analysis, CD105/CD133 cannot be validated as cancer stem cell markers of pRCC cell lines.
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spelling pubmed-52172072017-01-09 Functional significance of CD105-positive cells in papillary renal cell carcinoma Matak, Damian Brodaczewska, Klaudia K. Szczylik, Cezary Koch, Irena Myszczyszyn, Adam Lipiec, Monika Lewicki, Slawomir Szymanski, Lukasz Zdanowski, Robert Czarnecka, Anna M. BMC Cancer Research Article BACKGROUND: CD105 was postulated as a renal cell carcinoma (RCC) stem cell marker, and CD133 as a putative RCC progenitor. Hypoxia, a natural microenvironment that prevails in tumors, was also incorporated into the study, especially in terms of the promotion of hypothetical stem-like cell properties. METHODS: Within this study, we verify the existence of CD105+ and CD133+ populations in selected papillary subtype RCC (pRCC) cell lines. Both populations were analyzed for correlation with stem-like cell properties, such as stemness gene expression, and sphere and colony formation. For the preliminary analysis, several RCC cell lines were chosen (786-O, SMKT-R2, Caki-2, 796-P, ACHN, RCC6) and the control was human kidney cancer stem cells (HKCSC) and renal cells of embryonic origin (ASE-5063). Four cell lines were chosen for further investigation: Caki-2 (one of the highest numbers of CD105+ cells; primary origin), ACHN (a low number of CD105+ cells; metastatic origin), HKCSC (putative positive control), and ASE-5063 (additional control). RESULTS: In 769-P and RCC6, we could not detect a CD105+ population. Hypoxia variously affects pRCC cell growth, and mainly diminishes the stem-like properties of cells. Furthermore, we could not observe the correlation of CD105 and/or CD133 expression with the enhancement of stem-like properties. CONCLUSIONS: Based on this analysis, CD105/CD133 cannot be validated as cancer stem cell markers of pRCC cell lines. BioMed Central 2017-01-05 /pmc/articles/PMC5217207/ /pubmed/28056882 http://dx.doi.org/10.1186/s12885-016-2985-7 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Matak, Damian
Brodaczewska, Klaudia K.
Szczylik, Cezary
Koch, Irena
Myszczyszyn, Adam
Lipiec, Monika
Lewicki, Slawomir
Szymanski, Lukasz
Zdanowski, Robert
Czarnecka, Anna M.
Functional significance of CD105-positive cells in papillary renal cell carcinoma
title Functional significance of CD105-positive cells in papillary renal cell carcinoma
title_full Functional significance of CD105-positive cells in papillary renal cell carcinoma
title_fullStr Functional significance of CD105-positive cells in papillary renal cell carcinoma
title_full_unstemmed Functional significance of CD105-positive cells in papillary renal cell carcinoma
title_short Functional significance of CD105-positive cells in papillary renal cell carcinoma
title_sort functional significance of cd105-positive cells in papillary renal cell carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5217207/
https://www.ncbi.nlm.nih.gov/pubmed/28056882
http://dx.doi.org/10.1186/s12885-016-2985-7
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