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Gene expression profiling of circulating tumor cells and peripheral blood mononuclear cells from breast cancer patients
Circulating tumor cells (CTCs) are cancer cells that are released from a tumor into the bloodstream. The presence of CTCs in peripheral blood has been associated with metastasis formation in patients with breast cancer. Therefore, the molecular characterization of CTCs may improve diagnostics and su...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839342/ https://www.ncbi.nlm.nih.gov/pubmed/27141386 http://dx.doi.org/10.1080/2162402X.2015.1102827 |
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author | Hensler, Michal Vančurová, Irena Becht, Etienne Palata, Ondřej Strnad, Pavel Tesařová, Petra Čabiňaková, Michaela Švec, David Kubista, Mikael Bartůňková, Jiřina Špíšek, Radek Sojka, Luděk |
author_facet | Hensler, Michal Vančurová, Irena Becht, Etienne Palata, Ondřej Strnad, Pavel Tesařová, Petra Čabiňaková, Michaela Švec, David Kubista, Mikael Bartůňková, Jiřina Špíšek, Radek Sojka, Luděk |
author_sort | Hensler, Michal |
collection | PubMed |
description | Circulating tumor cells (CTCs) are cancer cells that are released from a tumor into the bloodstream. The presence of CTCs in peripheral blood has been associated with metastasis formation in patients with breast cancer. Therefore, the molecular characterization of CTCs may improve diagnostics and support treatment decisions. We performed gene expression profiling to evaluate the enriched CTCs and peripheral blood mononuclear cells (PBMCs) of breast cancer patients using an expression panel of 55 breast cancer-associated genes. The study revealed several significantly differentially expressed genes in the CTC-positive samples, including a few that were exclusively expressed in these cells. However, the expression of these genes was barely detectable in the PBMC samples. Some genes were differentially expressed in PBMCs, and the expression of these genes was correlated with tumor grade and the formation of metastasis. In this study, we have shown that the enriched CTCs of breast cancer patients overexpress genes involved in proteolytic degradation of the extracellular matrix (ECM) as well as genes that play important roles in the epithelial-mesenchymal transition (EMT) process that may occur in these cells. |
format | Online Article Text |
id | pubmed-4839342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-48393422016-05-02 Gene expression profiling of circulating tumor cells and peripheral blood mononuclear cells from breast cancer patients Hensler, Michal Vančurová, Irena Becht, Etienne Palata, Ondřej Strnad, Pavel Tesařová, Petra Čabiňaková, Michaela Švec, David Kubista, Mikael Bartůňková, Jiřina Špíšek, Radek Sojka, Luděk Oncoimmunology Original Research Circulating tumor cells (CTCs) are cancer cells that are released from a tumor into the bloodstream. The presence of CTCs in peripheral blood has been associated with metastasis formation in patients with breast cancer. Therefore, the molecular characterization of CTCs may improve diagnostics and support treatment decisions. We performed gene expression profiling to evaluate the enriched CTCs and peripheral blood mononuclear cells (PBMCs) of breast cancer patients using an expression panel of 55 breast cancer-associated genes. The study revealed several significantly differentially expressed genes in the CTC-positive samples, including a few that were exclusively expressed in these cells. However, the expression of these genes was barely detectable in the PBMC samples. Some genes were differentially expressed in PBMCs, and the expression of these genes was correlated with tumor grade and the formation of metastasis. In this study, we have shown that the enriched CTCs of breast cancer patients overexpress genes involved in proteolytic degradation of the extracellular matrix (ECM) as well as genes that play important roles in the epithelial-mesenchymal transition (EMT) process that may occur in these cells. Taylor & Francis 2015-12-10 /pmc/articles/PMC4839342/ /pubmed/27141386 http://dx.doi.org/10.1080/2162402X.2015.1102827 Text en © 2016 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License http://creativecommons.org/licenses/by-nc/3.0/, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted. |
spellingShingle | Original Research Hensler, Michal Vančurová, Irena Becht, Etienne Palata, Ondřej Strnad, Pavel Tesařová, Petra Čabiňaková, Michaela Švec, David Kubista, Mikael Bartůňková, Jiřina Špíšek, Radek Sojka, Luděk Gene expression profiling of circulating tumor cells and peripheral blood mononuclear cells from breast cancer patients |
title | Gene expression profiling of circulating tumor cells and peripheral blood mononuclear cells from breast cancer patients |
title_full | Gene expression profiling of circulating tumor cells and peripheral blood mononuclear cells from breast cancer patients |
title_fullStr | Gene expression profiling of circulating tumor cells and peripheral blood mononuclear cells from breast cancer patients |
title_full_unstemmed | Gene expression profiling of circulating tumor cells and peripheral blood mononuclear cells from breast cancer patients |
title_short | Gene expression profiling of circulating tumor cells and peripheral blood mononuclear cells from breast cancer patients |
title_sort | gene expression profiling of circulating tumor cells and peripheral blood mononuclear cells from breast cancer patients |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839342/ https://www.ncbi.nlm.nih.gov/pubmed/27141386 http://dx.doi.org/10.1080/2162402X.2015.1102827 |
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