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Updated: Jun 5, 2025

A Next-generation Tissue Microarray ngTMA Protocol for Biomarker Studies
Published on: September 23, 2014
Carcinoembryonic Antigen Expression in Human Tumors: A Tissue Microarray Study on 13,725 Tumors
Kristina Jansen1, Lara Kornfeld2, Maximilian Lennartz2
1Department of General, Visceral, and Thoracic Surgery, University Medical Center Hamburg-Eppendorf, 20251 Hamburg, Germany.
Carcinoembryonic antigen (CEA) is widely expressed in many epithelial cancers, not just colorectal. This study mapped CEA expression across 120 tumor types, finding it in over half, highlighting its potential for cancer monitoring and therapy.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Biomarkers
Background:
- Carcinoembryonic antigen (CEA) is a cell-surface glycoprotein with established roles in cancer diagnostics and monitoring.
- Existing data on CEA expression prevalence in various cancer tissues are inconsistent.
- Understanding CEA expression patterns is crucial for its therapeutic and diagnostic applications.
Purpose of the Study:
- To comprehensively determine the prevalence of CEA expression in a wide array of normal and neoplastic human tissues.
- To identify specific tumor types exhibiting significant CEA expression.
- To correlate CEA expression with clinical parameters and molecular features.
Main Methods:
- Analysis of a large-scale tissue microarray (TMA) comprising 13,725 samples.
- Inclusion of 120 distinct tumor types and 76 normal tissue types.
- Immunohistochemistry (IHC) was employed to detect CEA expression.
Main Results:
- CEA was detected in 54.2% (65/120) of tumor types, with strong positivity in 40.8%.
- High CEA prevalence was observed in colorectal adenomas/carcinomas, thyroid medullary carcinomas, pulmonary adenocarcinomas, and ovarian mucinous carcinomas.
- CEA overexpression correlated with tumor grade and invasiveness in bladder cancer, and with hormone receptor/HER2 status in breast cancer.
Conclusions:
- CEA is broadly expressed across a diverse range of epithelial neoplasms.
- The findings support the utility of CEA for serum monitoring and targeted anti-CEA therapies in numerous cancer types.
- This study provides a valuable resource for understanding CEA's role in oncogenesis and its clinical potential.
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