Original Article

Modern Pathology (2009) 22, 182–190; doi:10.1038/modpathol.2008.123; published online 11 July 2008

N-cadherin serves as diagnostic biomarker in intrahepatic and perihilar cholangiocarcinomas

Jean-François Mosnier1,2,3, Christine Kandel1,2, Dominique Cazals-Hatem4, Chantal Bou-Hanna1, Jérome Gournay2, Anne Jarry1 and Christian L Laboisse1,2

  1. 1Université de Nantes, Faculté de Médecine de Nantes, EA Biometadys, Nantes, France
  2. 2CHU de Nantes, Nantes, France
  3. 3Tumorothèque de l'IRCNA, Nantes, France
  4. 4Service d'Anatomie et de Cytologie Pathologiques, Assistance Publique—Hôpitaux de Paris, Hôpital Beaujon, Clichy, France

Correspondence: Professor J-F Mosnier, CHU Nantes, Service d'Anatomie et Cytologie Pathologiques, EA Biométadys, Universite de Nantes, Faculté de Médecine, 1 rue Gaston Veil, Nantes 44035, France. E-mail: jfmosnier@chu-nantes.fr

Received 4 November 2007; Revised 4 June 2008; Accepted 5 June 2008; Published online 11 July 2008.

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Abstract

As a definite immunoprofile of this tumor is missing, the histopathologic diagnosis of intrahepatic cholangiocarcinoma is difficult. The aim of this study was to explore E- and N-cadherin expressions in intrahepatic bile duct tumors, and to determine their potential interest in differential diagnosis. Normal liver tissue, 5 cirrhosis with ductular reaction, 5 focal nodular hyperplasia, 5 bile duct hamartomas, 5 bile duct adenomas, and 45 intrahepatic cholangiocarcinomas from Causasian patients were studied. Tissue-microarrays including 20 esophageal, 86 gastric, 8 small bowel, 64 colonic, 18 pancreatic, 6 gallbladder, and 7 extrahepatic biliary tract adenocarcinomas, 22 hepatocellular carcinomas, and normal tissues were constructed. Immunohistochemistry was performed using E-cadherin, N-cadherin, NCAM, Hep Par1, and cytokeratins 7, 19 and 20. Immunoblot analysis of frozen liver tissues was performed to control the specificity of E- and N-cadherin antibodies used. In normal liver, epithelial cells of intrahepatic bile ducts, whatever their caliber, as well as hepatocytes, coexpressed E- and N-cadherins at their plasma membranes. In cirrhosis, ductular reactions completely expressed E- and N-cadherins. All the benign lesions and 30 of the 45 intrahepatic cholangiocarcinomas (23/29 peripheral and 7/16 hilar) also expressed N-cadherin. E-cadherin was detected in all the lesions. The expression of N-cadherin at the plasma membrane of tumor cells was significantly more frequent in peripheral than in hilar intrahepatic cholangiocarcinomas (P=0.003). Among noncholangiocarcinomas, only 1% gastric and 66% gallbladder adenocarcinomas and all the hepatocellular carcinomas expressed N-cadherin at the membrane of tumor cells. Finally, for the diagnosis of intrahepatic cholangiocarcinomas, the specificity value of membranous expression of N-cadherin was 88%, whereas that of the combination cytokeratin 7/membranous N-cadherin was 98%. In the gastrointestinal and liver tract, membranous N-cadherin is restricted to the hepatocytes and intrahepatic biliary cells. In combination with cytokeratin 7 and Hep Par1, N-cadherin is a reliable tool for the histopathological diagnosis of primary hepatic tumors.

Keywords:

N-cadherin, E-cadherin, cholangiocarcinoma, tissue microarrays

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