Your browser doesn't support javascript.
loading
Epithelial Cell Adhesion Molecule (EpCAM) Expression in Human Tumors: A Comparison with Pan-Cytokeratin and TROP2 in 14,832 Tumors.
Menz, Anne; Lony, Nora; Lennartz, Maximilian; Dwertmann Rico, Sebastian; Schlichter, Ria; Kind, Simon; Reiswich, Viktor; Viehweger, Florian; Dum, David; Luebke, Andreas M; Kluth, Martina; Gorbokon, Natalia; Hube-Magg, Claudia; Bernreuther, Christian; Simon, Ronald; Clauditz, Till S; Sauter, Guido; Hinsch, Andrea; Jacobsen, Frank; Marx, Andreas H; Steurer, Stefan; Minner, Sarah; Burandt, Eike; Krech, Till; Lebok, Patrick; Weidemann, Sören.
Affiliation
  • Menz A; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Lony N; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Lennartz M; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Dwertmann Rico S; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Schlichter R; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Kind S; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Reiswich V; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Viehweger F; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Dum D; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Luebke AM; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Kluth M; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Gorbokon N; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Hube-Magg C; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Bernreuther C; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Simon R; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Clauditz TS; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Sauter G; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Hinsch A; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Jacobsen F; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Marx AH; Department of Pathology, Academic Hospital Fuerth, 90766 Fuerth, Germany.
  • Steurer S; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Minner S; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Burandt E; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Krech T; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Lebok P; Institute of Pathology, Clinical Center Osnabrueck, 49076 Osnabrueck, Germany.
  • Weidemann S; Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Diagnostics (Basel) ; 14(10)2024 May 17.
Article in En | MEDLINE | ID: mdl-38786342
ABSTRACT
EpCAM is expressed in many epithelial tumors and is used for the distinction of malignant mesotheliomas from adenocarcinomas and as a surrogate pan-epithelial marker. A tissue microarray containing 14,832 samples from 120 different tumor categories was analyzed by immunohistochemistry. EpCAM staining was compared with TROP2 and CKpan. EpCAM staining was detectable in 99 tumor categories. Among 78 epithelial tumor types, the EpCAM positivity rate was ≥90% in 60 categories-including adenocarcinomas, neuroendocrine neoplasms, and germ cell tumors. EpCAM staining was the lowest in hepatocellular carcinomas, adrenocortical tumors, renal cell neoplasms, and in poorly differentiated carcinomas. A comparison of EpCAM and CKpan staining identified a high concordance but EpCAM was higher in testicular seminomas and neuroendocrine neoplasms and CKpan in hepatocellular carcinomas, mesotheliomas, and poorly differentiated non-neuroendocrine tumors. A comparison of EpCAM and TROP2 revealed a higher rate of TROP2 positivity in squamous cell carcinomas and lower rates in many gastrointestinal adenocarcinomas, testicular germ cell tumors, neuroendocrine neoplasms, and renal cell tumors. These data confirm EpCAM as a surrogate epithelial marker for adenocarcinomas and its diagnostic utility for the distinction of malignant mesotheliomas. In comparison to CKpan and TROP2 antibodies, EpCAM staining is particularly common in seminomas and in neuroendocrine neoplasms.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Diagnostics (Basel) Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Diagnostics (Basel) Year: 2024 Document type: Article Affiliation country: Country of publication: