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
- 1Université de Nantes, Faculté de Médecine de Nantes, EA Biometadys, Nantes, France
- 2CHU de Nantes, Nantes, France
- 3Tumorothèque de l'IRCNA, Nantes, France
- 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.
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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