Epithelial Cell Adhesion Molecule (EpCAM) Expression in Human Tumors: A Comparison with Pan-Cytokeratin and TROP2 in 14,832 Tumors
- Anne Menz 1, Nora Lony 1, Maximilian Lennartz 1, Sebastian Dwertmann Rico 1, Ria Schlichter 1, Simon Kind 1, Viktor Reiswich 1, Florian Viehweger 1, David Dum 1, Andreas M Luebke 1, Martina Kluth 1, Natalia Gorbokon 1, Claudia Hube-Magg 1, Christian Bernreuther 1, Ronald Simon 1, Till S Clauditz 1, Guido Sauter 1, Andrea Hinsch 1, Frank Jacobsen 1, Andreas H Marx 2, Stefan Steurer 1, Sarah Minner 1, Eike Burandt 1, Till Krech 1,3, Patrick Lebok 1,3, Sören Weidemann 1
- Anne Menz 1, Nora Lony 1, Maximilian Lennartz 1
- 1Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
- 2Department of Pathology, Academic Hospital Fuerth, 90766 Fuerth, Germany.
- 3Institute of Pathology, Clinical Center Osnabrueck, 49076 Osnabrueck, Germany.
- 0Institute of Pathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
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View abstract on PubMed
Summary
This summary is machine-generated.EpCAM is a reliable epithelial marker found in most tumors, useful for distinguishing malignant mesotheliomas from adenocarcinomas. Its expression is high in many tumor types, including neuroendocrine neoplasms and seminomas.
Area Of Science
- Oncology
- Pathology
- Immunohistochemistry
Background
- Epithelial cell adhesion molecule (EpCAM) is a transmembrane glycoprotein expressed in various epithelial tissues.
- It serves as a diagnostic marker for distinguishing malignant mesotheliomas from adenocarcinomas and acts as a pan-epithelial marker.
- Understanding EpCAM expression patterns across diverse tumor types is crucial for accurate diagnosis and targeted therapies.
Purpose Of The Study
- To comprehensively evaluate the expression profile of EpCAM across a large and diverse set of human tumors.
- To compare EpCAM staining with other established markers like TROP2 and Cytokeratin Pan (CKpan).
- To confirm the utility of EpCAM as a diagnostic marker for specific tumor types, including malignant mesotheliomas and neuroendocrine neoplasms.
Main Methods
- Immunohistochemistry was performed on a large-scale tissue microarray (TMA) comprising 14,832 samples from 120 different tumor categories.
- EpCAM staining intensity and positivity rates were analyzed and compared with TROP2 and CKpan expression data.
- Statistical analysis was used to determine concordance and differences in marker expression across tumor types.
Main Results
- EpCAM staining was detected in 99 out of 120 tumor categories, with positivity rates of ≥90% in 60 epithelial tumor types, including adenocarcinomas, neuroendocrine neoplasms, and germ cell tumors.
- EpCAM showed high concordance with CKpan but was more frequently expressed in testicular seminomas and neuroendocrine neoplasms.
- Compared to TROP2, EpCAM exhibited lower positivity in squamous cell carcinomas but higher rates in several gastrointestinal adenocarcinomas and renal cell tumors.
Conclusions
- EpCAM is a highly sensitive surrogate epithelial marker, particularly valuable for diagnosing adenocarcinomas.
- EpCAM expression is significantly higher in seminomas and neuroendocrine neoplasms compared to CKpan and TROP2, enhancing its diagnostic utility in these entities.
- The study confirms EpCAM's diagnostic value in distinguishing malignant mesotheliomas from adenocarcinomas and highlights its broad applicability in oncological pathology.
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