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Levels of Soluble E-Cadherin in Breast, Gastric, and Colorectal Cancers

Soluble E-cadherin is a 80 kDa protein fragment coming from the proteolytic cleavage of the extracellular domain of the full length epithelial cadherin, a molecule involved in cell adhesion/polarity and tissue morphogenesis. In comparison with normal epithelia, cancer cells show a decreased cadherin...

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Detalles Bibliográficos
Autores principales: Repetto, Ombretta, De Paoli, Paolo, De Re, Valli, Canzonieri, Vincenzo, Cannizzaro, Renato
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4182303/
https://www.ncbi.nlm.nih.gov/pubmed/25535613
http://dx.doi.org/10.1155/2014/408047
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author Repetto, Ombretta
De Paoli, Paolo
De Re, Valli
Canzonieri, Vincenzo
Cannizzaro, Renato
author_facet Repetto, Ombretta
De Paoli, Paolo
De Re, Valli
Canzonieri, Vincenzo
Cannizzaro, Renato
author_sort Repetto, Ombretta
collection PubMed
description Soluble E-cadherin is a 80 kDa protein fragment coming from the proteolytic cleavage of the extracellular domain of the full length epithelial cadherin, a molecule involved in cell adhesion/polarity and tissue morphogenesis. In comparison with normal epithelia, cancer cells show a decreased cadherin-mediated intercellular adhesion, and sE-cad levels normally increase in body fluids (blood and urine). This review focuses on soluble E-cadherin in sera of patients affected by three solid cancers (breast, gastric, and colorectal cancers) and how its levels correlate or not with some cancer parameters (e.g., dimension, progression, and localisation). We will describe the main proteomics approaches adopted to measure sE-cad both in vivo and in vitro and the most important findings about its behaviour in cancer dynamics.
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spelling pubmed-41823032014-12-22 Levels of Soluble E-Cadherin in Breast, Gastric, and Colorectal Cancers Repetto, Ombretta De Paoli, Paolo De Re, Valli Canzonieri, Vincenzo Cannizzaro, Renato Biomed Res Int Review Article Soluble E-cadherin is a 80 kDa protein fragment coming from the proteolytic cleavage of the extracellular domain of the full length epithelial cadherin, a molecule involved in cell adhesion/polarity and tissue morphogenesis. In comparison with normal epithelia, cancer cells show a decreased cadherin-mediated intercellular adhesion, and sE-cad levels normally increase in body fluids (blood and urine). This review focuses on soluble E-cadherin in sera of patients affected by three solid cancers (breast, gastric, and colorectal cancers) and how its levels correlate or not with some cancer parameters (e.g., dimension, progression, and localisation). We will describe the main proteomics approaches adopted to measure sE-cad both in vivo and in vitro and the most important findings about its behaviour in cancer dynamics. Hindawi Publishing Corporation 2014 2014-09-16 /pmc/articles/PMC4182303/ /pubmed/25535613 http://dx.doi.org/10.1155/2014/408047 Text en Copyright © 2014 Ombretta Repetto et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Repetto, Ombretta
De Paoli, Paolo
De Re, Valli
Canzonieri, Vincenzo
Cannizzaro, Renato
Levels of Soluble E-Cadherin in Breast, Gastric, and Colorectal Cancers
title Levels of Soluble E-Cadherin in Breast, Gastric, and Colorectal Cancers
title_full Levels of Soluble E-Cadherin in Breast, Gastric, and Colorectal Cancers
title_fullStr Levels of Soluble E-Cadherin in Breast, Gastric, and Colorectal Cancers
title_full_unstemmed Levels of Soluble E-Cadherin in Breast, Gastric, and Colorectal Cancers
title_short Levels of Soluble E-Cadherin in Breast, Gastric, and Colorectal Cancers
title_sort levels of soluble e-cadherin in breast, gastric, and colorectal cancers
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4182303/
https://www.ncbi.nlm.nih.gov/pubmed/25535613
http://dx.doi.org/10.1155/2014/408047
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