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Epithelial Cell Adhesion Molecule: An Anchor to Isolate Clinically Relevant Circulating Tumor Cells

In the last few decades, the epithelial cell adhesion molecule (EpCAM) has received increased attention as the main membrane marker used in many enrichment technologies to isolate circulating tumor cells (CTCs). Although there has been a great deal of progress in the implementation of EpCAM-based CT...

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Autores principales: Eslami-S, Zahra, Cortés-Hernández, Luis Enrique, Alix-Panabières, Catherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7464831/
https://www.ncbi.nlm.nih.gov/pubmed/32764280
http://dx.doi.org/10.3390/cells9081836
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author Eslami-S, Zahra
Cortés-Hernández, Luis Enrique
Alix-Panabières, Catherine
author_facet Eslami-S, Zahra
Cortés-Hernández, Luis Enrique
Alix-Panabières, Catherine
author_sort Eslami-S, Zahra
collection PubMed
description In the last few decades, the epithelial cell adhesion molecule (EpCAM) has received increased attention as the main membrane marker used in many enrichment technologies to isolate circulating tumor cells (CTCs). Although there has been a great deal of progress in the implementation of EpCAM-based CTC detection technologies in medical settings, several issues continue to limit their clinical utility. The biology of EpCAM and its role are not completely understood but evidence suggests that the expression of this epithelial cell-surface protein is crucial for metastasis-competent CTCs and may not be lost completely during the epithelial-to-mesenchymal transition. In this review, we summarize the most significant advantages and disadvantages of using EpCAM as a marker for CTC enrichment and its potential biological role in the metastatic cascade.
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spelling pubmed-74648312020-09-04 Epithelial Cell Adhesion Molecule: An Anchor to Isolate Clinically Relevant Circulating Tumor Cells Eslami-S, Zahra Cortés-Hernández, Luis Enrique Alix-Panabières, Catherine Cells Review In the last few decades, the epithelial cell adhesion molecule (EpCAM) has received increased attention as the main membrane marker used in many enrichment technologies to isolate circulating tumor cells (CTCs). Although there has been a great deal of progress in the implementation of EpCAM-based CTC detection technologies in medical settings, several issues continue to limit their clinical utility. The biology of EpCAM and its role are not completely understood but evidence suggests that the expression of this epithelial cell-surface protein is crucial for metastasis-competent CTCs and may not be lost completely during the epithelial-to-mesenchymal transition. In this review, we summarize the most significant advantages and disadvantages of using EpCAM as a marker for CTC enrichment and its potential biological role in the metastatic cascade. MDPI 2020-08-05 /pmc/articles/PMC7464831/ /pubmed/32764280 http://dx.doi.org/10.3390/cells9081836 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Eslami-S, Zahra
Cortés-Hernández, Luis Enrique
Alix-Panabières, Catherine
Epithelial Cell Adhesion Molecule: An Anchor to Isolate Clinically Relevant Circulating Tumor Cells
title Epithelial Cell Adhesion Molecule: An Anchor to Isolate Clinically Relevant Circulating Tumor Cells
title_full Epithelial Cell Adhesion Molecule: An Anchor to Isolate Clinically Relevant Circulating Tumor Cells
title_fullStr Epithelial Cell Adhesion Molecule: An Anchor to Isolate Clinically Relevant Circulating Tumor Cells
title_full_unstemmed Epithelial Cell Adhesion Molecule: An Anchor to Isolate Clinically Relevant Circulating Tumor Cells
title_short Epithelial Cell Adhesion Molecule: An Anchor to Isolate Clinically Relevant Circulating Tumor Cells
title_sort epithelial cell adhesion molecule: an anchor to isolate clinically relevant circulating tumor cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7464831/
https://www.ncbi.nlm.nih.gov/pubmed/32764280
http://dx.doi.org/10.3390/cells9081836
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