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      Prognostic significance of epithelial–mesenchymal transition-related markers in extrahepatic cholangiocarcinoma: comprehensive immunohistochemical study using a tissue microarray

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          Abstract

          Background:

          Epithelial–mesenchymal transition (EMT) is characterised by the loss of cell-to-cell adhesion and gaining of mesenchymal phenotypes. Epithelial–mesenchymal transition is proposed to occur in various developmental processes and cancer progression. ‘Cadherin switch', a process in which cells shift to express different isoforms of the cadherin transmembrane protein and usually refers to a switch from the expression of E-cadherin to N-cadherin, is one aspect of EMT and can have a profound effect on tumour invasion/metastasis. The aim of this study was to investigate the clinicopathological significance of EMT-related proteins and cadherin switch in extrahepatic cholangiocarcinoma (EHCC).

          Methods:

          We investigated the association between altered expression of 12 EMT-related proteins and clinical outcomes in patients with EHCC ( n=117) using immunohistochemistry on tissue microarrays.

          Results:

          Univariate and multivariate analyses revealed that, in addition to N classification ( P=0.0420), the expression of E-cadherin ( P=0.0208), N-cadherin ( P=0.0038) and S100A4 ( P=0.0157) was each an independent and a significant prognostic factor. We also demonstrated that cadherin switch was independently associated with poor prognosis ( P=0.0143) in patients with EHCC.

          Conclusions:

          These results may provide novel information for selection of patients with EHCC who require adjuvant therapy and strict surveillance.

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          Most cited references35

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          Epithelial-mesenchymal transitions in development and disease.

          The epithelial to mesenchymal transition (EMT) plays crucial roles in the formation of the body plan and in the differentiation of multiple tissues and organs. EMT also contributes to tissue repair, but it can adversely cause organ fibrosis and promote carcinoma progression through a variety of mechanisms. EMT endows cells with migratory and invasive properties, induces stem cell properties, prevents apoptosis and senescence, and contributes to immunosuppression. Thus, the mesenchymal state is associated with the capacity of cells to migrate to distant organs and maintain stemness, allowing their subsequent differentiation into multiple cell types during development and the initiation of metastasis.
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            Cholangiocarcinoma: thirty-one-year experience with 564 patients at a single institution.

            To assess long-term survival and prognostic factors in a large series of patients with bile duct cancer. The incidence of bile duct cancer is low but increasing. Determinants of survival vary in the literature, due to a lack of sufficient numbers of patients in most series. We studied 564 consecutive patients with bile duct cancer operated upon between 1973 and 2004. Patients were divided into intrahepatic, perihilar, and distal groups. Principle outcome measures were complications, 30-day mortality, and survival. Of the 564 patients, 44 (8%) had intrahepatic, 281 (50%) had perihilar, and 239 (42%) had distal tumors. Approximately half (294, 52%) were treated before 1995, while 270 (48%) were treated thereafter. The perioperative mortality rate was 4%. In log-rank analyses, survival was higher in the later time period (P = 0.002), in patients with intrahepatic disease (P = 0.001), with negative resection margins (P < 0.001), with well/moderately differentiated tumors (P < 0.001), and those with negative lymph nodal status (P < 0.001). In multivariate analysis, negative margins (P < 0.001), tumor differentiation (P < 0.001), and negative nodal status (P < 0.001), but not tumor diameter, were significant independent prognostic factors. In R0-resected patients, lymph node status (P < 0.001), but not tumor diameter, histology, or differentiation, further predicted survival. The median survivals for R0-resected intrahepatic, perihilar, and distal tumors were 80, 30, and 25 months, respectively, and the 5-year survivals were 63%, 30%, and 27%, respectively. R0 resection remains the best chance for long-term survival, and lymph node status is the most important prognostic factor following R0 resection.
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              Cadherin switching.

              The cadherin molecules at adherens junctions have multiple isoforms. Cadherin isoform switching (cadherin switching) occurs during normal developmental processes to allow cell types to segregate from one another. Tumor cells often recapitulate this activity and the result is an aggressive tumor cell that gains the ability to leave the site of the tumor and metastasize. At present, we understand some of the mechanisms that promote cadherin switching and some of the pathways downstream of this process that influence cell behavior. Specific cadherin family members influence growth-factor-receptor signaling and Rho GTPases to promote cell motility and invasion. In addition, p120-catenin probably plays multiple roles in cadherin switching, regulating Rho GTPases and stabilizing cadherins.
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                Author and article information

                Journal
                Br J Cancer
                Br. J. Cancer
                British Journal of Cancer
                Nature Publishing Group
                0007-0920
                1532-1827
                23 September 2014
                31 July 2014
                : 111
                : 7
                : 1363-1372
                Affiliations
                [1 ]Department of Surgical Pathology, Hokkaido University Hospital , N14, W5, Kita-ku, Sapporo, Hokkaido 060-8648, Japan
                [2 ]Department of Gastroenterological Surgery II, Hokkaido University Graduate School of Medicine , N14, W5, Kita-ku, Sapporo, Hokkaido 060-8648, Japan
                [3 ]Translational Research and Clinical Trial Center, Hokkaido University Hospital , N14, W5, Kita-ku, Sapporo, Hokkaido 060-8648, Japan
                Author notes
                Article
                bjc2014415
                10.1038/bjc.2014.415
                4183847
                25077440
                8d4f4139-1467-43c8-ab84-a7d4336d6747
                Copyright © 2014 Cancer Research UK

                From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/

                History
                : 03 February 2014
                : 25 June 2014
                : 01 July 2014
                Categories
                Molecular Diagnostics

                Oncology & Radiotherapy
                emt,extrahepatic cholangiocarcinoma,immunohistochemistry,tissue microarray,prognosis,survival,cadherin switch

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