Canalicular immunostaining of neprilysin (CD10) as a diagnostic marker forhepatocellular carcinomas

Citation
N. Borscheri et al., Canalicular immunostaining of neprilysin (CD10) as a diagnostic marker forhepatocellular carcinomas, AM J SURG P, 25(10), 2001, pp. 1297-1303
Citations number
23
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research Diagnosis & Treatment
Journal title
AMERICAN JOURNAL OF SURGICAL PATHOLOGY
ISSN journal
01475185 → ACNP
Volume
25
Issue
10
Year of publication
2001
Pages
1297 - 1303
Database
ISI
SICI code
0147-5185(200110)25:10<1297:CION(A>2.0.ZU;2-4
Abstract
Neprilysin (CD 10) is expressed in both normal and neoplastic liver tissue, where it exhibits a characteristic canalicular pattern (CD10(can)) similar to the one observed when antibodies cross-react with biliary glycoprotein I (p-CEA). The aim of this retrospective study was to investigate the use o f CD10(can) in differentiating between hepatocellular carcinomas (HCCs; 63 specimens) and nonhepatocellular carcinomas (non-HCCs) metastatic to the li ver (non-HCC; 25 specimens). Immunostaining was performed with antibodies d irected against CD10, p-CEA, and a-fetoprotein (AFP). Albumin mRNA was dete cted by nonradioactive in situ hybridization (ISHalbumin). In the HCC group a canalicular staining pattern for CD10 was found in 43 (68.3%) specimens, AFP was found in 15 (23.8%) specimens, and a canalicular staining pattern for p-CEA was present in 60 (95.2%) specimens. ISH albumin was performed in 35 HCC specimens and showed labeling of tumor cells in 3 (85.7%) specimens . In the non-HCC group CD10(can), and p-CEA, immunostaining for AFP and lab eling for ISH albumin were confined to non-neoplastic liver tissue. Sensiti vity and specificity were, respectively, 68.3% and 100% for CD10(can), 23.8 % and 100% for AFP, 95.2% and 100% for canalicular p-CEA, and 86.4% and 100 % for ISHalbumin. Our results demonstrate that canalicular staining for CD1 0 is a highly specific marker of hepatocytic differentiation. Although it d oes not differentiate between benign and malignant lesions, CD10(can) is cl early useful in differentiating between HCC and non-HCC.