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Anti-Epithelial Cell Adhesion Molecule Antibodies and the Detection of Circulating Normal-Like Breast Tumor Cells

Identification of specific subtypes of circulating tumor cells in peripheral blood of cancer patients can provide information about the biology of metastasis and improve patient management. However, to be effective, the method used to identify circulating tumor cells must detect all tumor cell types...

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Autores principales: Sieuwerts, Anieta M., Kraan, Jaco, Bolt, Joan, van der Spoel, Petra, Elstrodt, Fons, Schutte, Mieke, Martens, John W. M., Gratama, Jan-Willem, Sleijfer, Stefan, Foekens, John A.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2639293/
https://www.ncbi.nlm.nih.gov/pubmed/19116383
http://dx.doi.org/10.1093/jnci/djn419
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author Sieuwerts, Anieta M.
Kraan, Jaco
Bolt, Joan
van der Spoel, Petra
Elstrodt, Fons
Schutte, Mieke
Martens, John W. M.
Gratama, Jan-Willem
Sleijfer, Stefan
Foekens, John A.
author_facet Sieuwerts, Anieta M.
Kraan, Jaco
Bolt, Joan
van der Spoel, Petra
Elstrodt, Fons
Schutte, Mieke
Martens, John W. M.
Gratama, Jan-Willem
Sleijfer, Stefan
Foekens, John A.
author_sort Sieuwerts, Anieta M.
collection PubMed
description Identification of specific subtypes of circulating tumor cells in peripheral blood of cancer patients can provide information about the biology of metastasis and improve patient management. However, to be effective, the method used to identify circulating tumor cells must detect all tumor cell types. We investigated whether the five subtypes of human breast cancer cells that have been defined by global gene expression profiling—normal-like, basal, HER2-positive, and luminal A and B—were identified by CellSearch, a US Food and Drug Administration–approved test that uses antibodies against the cell surface–expressed epithelial cell adhesion molecule (EpCAM) to isolate circulating tumor cells. We used global gene expression profiling to determine the subtypes of a well-defined panel of 34 human breast cancer cell lines (15 luminal, nine normal-like, five basal-like, and five Her2-positive). We mixed 50-150 cells from 10 of these cell lines with 7.5 mL of blood from a single healthy human donor, and the mixtures were subjected to the CellSearch test to isolate the breast cancer cells. We found that the CellSearch isolation method, which uses EpCAM on the surface of circulating tumor cells for cell isolation, did not recognize, in particular, normal-like breast cancer cells, which in general have aggressive features. New tests that include antibodies that specifically recognize normal-like breast tumor cells but not cells of hematopoietic origin are needed.
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spelling pubmed-26392932009-02-25 Anti-Epithelial Cell Adhesion Molecule Antibodies and the Detection of Circulating Normal-Like Breast Tumor Cells Sieuwerts, Anieta M. Kraan, Jaco Bolt, Joan van der Spoel, Petra Elstrodt, Fons Schutte, Mieke Martens, John W. M. Gratama, Jan-Willem Sleijfer, Stefan Foekens, John A. J Natl Cancer Inst Brief Communication Identification of specific subtypes of circulating tumor cells in peripheral blood of cancer patients can provide information about the biology of metastasis and improve patient management. However, to be effective, the method used to identify circulating tumor cells must detect all tumor cell types. We investigated whether the five subtypes of human breast cancer cells that have been defined by global gene expression profiling—normal-like, basal, HER2-positive, and luminal A and B—were identified by CellSearch, a US Food and Drug Administration–approved test that uses antibodies against the cell surface–expressed epithelial cell adhesion molecule (EpCAM) to isolate circulating tumor cells. We used global gene expression profiling to determine the subtypes of a well-defined panel of 34 human breast cancer cell lines (15 luminal, nine normal-like, five basal-like, and five Her2-positive). We mixed 50-150 cells from 10 of these cell lines with 7.5 mL of blood from a single healthy human donor, and the mixtures were subjected to the CellSearch test to isolate the breast cancer cells. We found that the CellSearch isolation method, which uses EpCAM on the surface of circulating tumor cells for cell isolation, did not recognize, in particular, normal-like breast cancer cells, which in general have aggressive features. New tests that include antibodies that specifically recognize normal-like breast tumor cells but not cells of hematopoietic origin are needed. Oxford University Press 2009-01-07 2009-01-07 /pmc/articles/PMC2639293/ /pubmed/19116383 http://dx.doi.org/10.1093/jnci/djn419 Text en © 2008 The Author(s). This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Communication
Sieuwerts, Anieta M.
Kraan, Jaco
Bolt, Joan
van der Spoel, Petra
Elstrodt, Fons
Schutte, Mieke
Martens, John W. M.
Gratama, Jan-Willem
Sleijfer, Stefan
Foekens, John A.
Anti-Epithelial Cell Adhesion Molecule Antibodies and the Detection of Circulating Normal-Like Breast Tumor Cells
title Anti-Epithelial Cell Adhesion Molecule Antibodies and the Detection of Circulating Normal-Like Breast Tumor Cells
title_full Anti-Epithelial Cell Adhesion Molecule Antibodies and the Detection of Circulating Normal-Like Breast Tumor Cells
title_fullStr Anti-Epithelial Cell Adhesion Molecule Antibodies and the Detection of Circulating Normal-Like Breast Tumor Cells
title_full_unstemmed Anti-Epithelial Cell Adhesion Molecule Antibodies and the Detection of Circulating Normal-Like Breast Tumor Cells
title_short Anti-Epithelial Cell Adhesion Molecule Antibodies and the Detection of Circulating Normal-Like Breast Tumor Cells
title_sort anti-epithelial cell adhesion molecule antibodies and the detection of circulating normal-like breast tumor cells
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2639293/
https://www.ncbi.nlm.nih.gov/pubmed/19116383
http://dx.doi.org/10.1093/jnci/djn419
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