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Flow Cytometric Analysis of CD133- and EpCAM-Positive Cells in the Peripheral Blood of Patients with Lung Cancer

Lung tumors are characterized by their high metastatic potential, which is the main cause of therapeutic failure. However, the exact cellular origin of metastasis remains unknown. Since the introduction of the cancer stem cell theory, lung cancer stem cells (LCSCs) have been thought to represent met...

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Autores principales: Skirecki, Tomasz, Hoser, Grażyna, Kawiak, Jerzy, Dziedzic, Dariusz, Domagała-Kulawik, Joanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Basel 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898538/
https://www.ncbi.nlm.nih.gov/pubmed/23959111
http://dx.doi.org/10.1007/s00005-013-0250-1
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author Skirecki, Tomasz
Hoser, Grażyna
Kawiak, Jerzy
Dziedzic, Dariusz
Domagała-Kulawik, Joanna
author_facet Skirecki, Tomasz
Hoser, Grażyna
Kawiak, Jerzy
Dziedzic, Dariusz
Domagała-Kulawik, Joanna
author_sort Skirecki, Tomasz
collection PubMed
description Lung tumors are characterized by their high metastatic potential, which is the main cause of therapeutic failure. However, the exact cellular origin of metastasis remains unknown. Since the introduction of the cancer stem cell theory, lung cancer stem cells (LCSCs) have been thought to represent metastasis-founding cells. The current study aimed to evaluate whether LCSCs could be found in the circulation. Expression of the stem cell markers CD133 and EpCAM was confirmed in tumor and normal lung tissue by flow cytometry. Then, this technique was further used to investigate the expression of CD133 and EpCAM in the peripheral blood of 41 patients with primary lung cancer. Putative LCSCs (CD133(+)EpCAM(+)) were present in 6/7 tumor samples, and CD133(+)EpCAM(+) cells were identified in the blood samples of 15 patients at a median level of 40/ml of blood. EpCAM(+) cells were detected in 60 % of the patients, and the number of these cells was higher in patients with adenocarcinoma than patients with squamous cell carcinoma and was also higher in patients with less advanced disease. Moreover, the frequency of this subpopulation significantly correlated with the circulating level of SSEA-4(+) cells. Additionally, CD133(+)EpCAM(−) cells were found in 87 % of the patients, and the numbers of these cells were significantly higher in patients with distant metastases and correlated with disease stage. This study confirmed the presence of an LCSC subpopulation with a CD133(+)EpCAM(+) phenotype in the tumors and blood of patients with lung cancer, and these results suggest an important role for CD133 and EpCAM in lung cancer progression and their potential application as novel biomarkers of the disease.
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spelling pubmed-38985382014-01-28 Flow Cytometric Analysis of CD133- and EpCAM-Positive Cells in the Peripheral Blood of Patients with Lung Cancer Skirecki, Tomasz Hoser, Grażyna Kawiak, Jerzy Dziedzic, Dariusz Domagała-Kulawik, Joanna Arch Immunol Ther Exp (Warsz) Original Article Lung tumors are characterized by their high metastatic potential, which is the main cause of therapeutic failure. However, the exact cellular origin of metastasis remains unknown. Since the introduction of the cancer stem cell theory, lung cancer stem cells (LCSCs) have been thought to represent metastasis-founding cells. The current study aimed to evaluate whether LCSCs could be found in the circulation. Expression of the stem cell markers CD133 and EpCAM was confirmed in tumor and normal lung tissue by flow cytometry. Then, this technique was further used to investigate the expression of CD133 and EpCAM in the peripheral blood of 41 patients with primary lung cancer. Putative LCSCs (CD133(+)EpCAM(+)) were present in 6/7 tumor samples, and CD133(+)EpCAM(+) cells were identified in the blood samples of 15 patients at a median level of 40/ml of blood. EpCAM(+) cells were detected in 60 % of the patients, and the number of these cells was higher in patients with adenocarcinoma than patients with squamous cell carcinoma and was also higher in patients with less advanced disease. Moreover, the frequency of this subpopulation significantly correlated with the circulating level of SSEA-4(+) cells. Additionally, CD133(+)EpCAM(−) cells were found in 87 % of the patients, and the numbers of these cells were significantly higher in patients with distant metastases and correlated with disease stage. This study confirmed the presence of an LCSC subpopulation with a CD133(+)EpCAM(+) phenotype in the tumors and blood of patients with lung cancer, and these results suggest an important role for CD133 and EpCAM in lung cancer progression and their potential application as novel biomarkers of the disease. Springer Basel 2013-08-20 2014 /pmc/articles/PMC3898538/ /pubmed/23959111 http://dx.doi.org/10.1007/s00005-013-0250-1 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Article
Skirecki, Tomasz
Hoser, Grażyna
Kawiak, Jerzy
Dziedzic, Dariusz
Domagała-Kulawik, Joanna
Flow Cytometric Analysis of CD133- and EpCAM-Positive Cells in the Peripheral Blood of Patients with Lung Cancer
title Flow Cytometric Analysis of CD133- and EpCAM-Positive Cells in the Peripheral Blood of Patients with Lung Cancer
title_full Flow Cytometric Analysis of CD133- and EpCAM-Positive Cells in the Peripheral Blood of Patients with Lung Cancer
title_fullStr Flow Cytometric Analysis of CD133- and EpCAM-Positive Cells in the Peripheral Blood of Patients with Lung Cancer
title_full_unstemmed Flow Cytometric Analysis of CD133- and EpCAM-Positive Cells in the Peripheral Blood of Patients with Lung Cancer
title_short Flow Cytometric Analysis of CD133- and EpCAM-Positive Cells in the Peripheral Blood of Patients with Lung Cancer
title_sort flow cytometric analysis of cd133- and epcam-positive cells in the peripheral blood of patients with lung cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898538/
https://www.ncbi.nlm.nih.gov/pubmed/23959111
http://dx.doi.org/10.1007/s00005-013-0250-1
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