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1000 Titel
  • Expression and function of epithelial cell adhesion molecule EpCAM: where are we after 40 years?
1000 Autor/in
  1. Gires, Olivier |
  2. Pan, Min |
  3. Schinke, Henrik |
  4. Canis, Martin |
  5. Baeuerle, Patrick A. |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-06-07
1000 Erschienen in
1000 Quellenangabe
  • 39(3):969-987
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s10555-020-09898-3 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7497325/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • EpCAM (epithelial cell adhesion molecule) was discovered four decades ago as a tumor antigen on colorectal carcinomas. Owing to its frequent and high expression on carcinomas and their metastases, EpCAM serves as a prognostic marker, a therapeutic target, and an anchor molecule on circulating and disseminated tumor cells (CTCs/DTCs), which are considered the major source for metastatic cancer cells. Today, EpCAM is reckoned as a multi-functional transmembrane protein involved in the regulation of cell adhesion, proliferation, migration, stemness, and epithelial-to-mesenchymal transition (EMT) of carcinoma cells. To fulfill these functions, EpCAM is instrumental in intra- and intercellular signaling as a full-length molecule and following regulated intramembrane proteolysis, generating functionally active extra- and intracellular fragments. Intact EpCAM and its proteolytic fragments interact with claudins, CD44, E-cadherin, epidermal growth factor receptor (EGFR), and intracellular signaling components of the WNT and Ras/Raf pathways, respectively. This plethora of functions contributes to shaping intratumor heterogeneity and partial EMT, which are major determinants of the clinical outcome of carcinoma patients. EpCAM represents a marker for the epithelial status of primary and systemic tumor cells and emerges as a measure for the metastatic capacity of CTCs. Consequentially, EpCAM has reclaimed potential as a prognostic marker and target on primary and systemic tumor cells.
1000 Sacherschließung
lokal Epithelial Cell Adhesion Molecule/metabolism [MeSH]
lokal Humans [MeSH]
lokal Liquid biopsy
lokal Metastasis
lokal Epithelial-Mesenchymal Transition [MeSH]
lokal Animals [MeSH]
lokal Neoplasms/metabolism [MeSH]
lokal Epithelial-to-mesenchymal transition
lokal Neoplasms/pathology [MeSH]
lokal Epithelial Cell Adhesion Molecule/biosynthesis [MeSH]
lokal Carcinoma
lokal Regulated intramembrane proteolysis
lokal EpCAM
lokal Non-Thematic Review
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0002-2292-7064|https://frl.publisso.de/adhoc/uri/UGFuLCBNaW4=|https://frl.publisso.de/adhoc/uri/U2NoaW5rZSwgSGVucmlr|https://frl.publisso.de/adhoc/uri/Q2FuaXMsIE1hcnRpbg==|https://frl.publisso.de/adhoc/uri/QmFldWVybGUsIFBhdHJpY2sgQS4=
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1000 Erstellt am 2023-11-18T08:49:07.595+0100
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