Nuclear signalling by tumour-associated antigen EpCAM

• Published in: Nature cell biology Vol. 11; no. 2; pp. 162 - 171
• Main Authors: Maetzel, Dorothea, Denzel, Sabine, Mack, Brigitte, Canis, Martin, Went, Philip, Benk, Michael, Kieu, Cuong, Papior, Peer, Baeuerle, Patrick A, Munz, Markus, Gires, Olivier
• Format: Journal Article
• Language: English
• Published: England Nature Publishing Group 01.02.2009
• Subjects: Active Transport, Cell Nucleus - physiology; ADAM Proteins - metabolism; ADAM17 Protein; Adhesion; Animals; Antibodies; Antigens; Antigens, Neoplasm - genetics; Antigens, Neoplasm - metabolism; beta Catenin - genetics; beta Catenin - metabolism; Cancer; Carcinoma - genetics; Carcinoma - metabolism; Cell adhesion & migration; Cell adhesion molecules; Cell Adhesion Molecules - genetics; Cell Adhesion Molecules - metabolism; Cell growth; Cell Membrane - genetics; Cell Membrane - metabolism; Cell Nucleus - genetics; Cell Nucleus - metabolism; Cell Proliferation; Cell Transformation, Neoplastic - genetics; Cell Transformation, Neoplastic - metabolism; Colonic Neoplasms - genetics; Colonic Neoplasms - metabolism; Deoxyribonucleic acid; DNA; Environmental health; Epithelial Cell Adhesion Molecule; Genetic aspects; Health aspects; Homeodomain Proteins - genetics; Homeodomain Proteins - metabolism; Humans; LIM-Homeodomain Proteins; Lymphoid Enhancer-Binding Factor 1 - genetics; Lymphoid Enhancer-Binding Factor 1 - metabolism; Male; Membrane proteins; Mice; Mitosis - physiology; Muscle Proteins - genetics; Muscle Proteins - metabolism; NIH 3T3 Cells; Otolaryngology; Peptides; Physiological aspects; Presenilin-2 - metabolism; Protein Structure, Tertiary; Signal Transduction - physiology; Transcription Factors - genetics; Transcription Factors - metabolism; Translocation; Tumor antigens; United States; Germany
• ISSN: 1465-7392; 1476-4679
• DOI: 10.1038/ncb1824

EpCAM was found to be overexpressed on epithelial progenitors, carcinomas and cancer-initiating cells. The role of EpCAM in proliferation, and its association with cancer is poorly explained by proposed cell adhesion functions. Here we show that regulated intramembrane proteolysis activates EpCAM as a mitogenic signal transducer in vitro and in vivo. This involves shedding of its ectodomain EpEX and nuclear translocation of its intracellular domain EpICD. Cleavage of EpCAM is sequentially catalysed by TACE and presenilin-2. Pharmacological inhibition or genetic silencing of either protease impairs growth-promoting signalling by EpCAM, which is compensated for by EpICD. Released EpICD associates with FHL2, beta-catenin and Lef-1 to form a nuclear complex that contacts DNA at Lef-1 consensus sites, induces gene transcription and is oncogenic in immunodeficient mice. In patients, EpICD was found in nuclei of colon carcinoma but not of normal tissue. Nuclear signalling of EpCAM explains how EpCAM functions in cell proliferation.