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Published in: Journal of Cancer Research and Clinical Oncology 7/2017

01-07-2017 | Original Article – Cancer Research

The extracellular domain of E cadherin linked to invasiveness in colorectal cancer: a new resistance and relapses monitoring serum-bio marker?

Authors: Niki Christou, Aurélie Perraud, Sabrina Blondy, Marie-Odile Jauberteau, Serge Battu, Muriel Mathonnet

Published in: Journal of Cancer Research and Clinical Oncology | Issue 7/2017

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Abstract

Purpose

Multiple studies have attempted to demonstrate the interest of the cell adhesion marker, E cadherin, as a diagnostic and prognosis marker in colorectal cancer (CRC). However, it was considered non specific.

Materials and methods

Studies were carried out with CRC cell lines and patients’ cohort operated for CRC. The expression of E cadherin was studied after 5 fluorouracil (5FU) treatment and correlated to CRC relapse, chemo-resistance and survival.

Results

In CRC cell lines derived from high tumor stages, extracellular domain of E cadherin expression decreased after 5FU treatment whereas it increased in supernatants. Interestingly, only specific cleaved forms at 55 kDa of E cadherin were detected in supernatants. In CRC surgical patients, more importantly concerning extracellular E cadherin domain, a decreased expression was observed in tissues in function of CRC stages whereas an increased expression was found in sera. Moreover, there is an increasing trend of survival with weak serum E cadherin secretion, reinforcing the implication of this protein in CRC evolution.

Discussion

The extracellular domain can be defined as a 5FU resistance marker and allow CRC monitoring.
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Metadata
Title
The extracellular domain of E cadherin linked to invasiveness in colorectal cancer: a new resistance and relapses monitoring serum-bio marker?
Authors
Niki Christou
Aurélie Perraud
Sabrina Blondy
Marie-Odile Jauberteau
Serge Battu
Muriel Mathonnet
Publication date
01-07-2017
Publisher
Springer Berlin Heidelberg
Published in
Journal of Cancer Research and Clinical Oncology / Issue 7/2017
Print ISSN: 0171-5216
Electronic ISSN: 1432-1335
DOI
https://doi.org/10.1007/s00432-017-2382-x

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