Table 1.
Phenotype markers of candidate cholangiocarcinoma cells of origin
Marker | Mature cholangiocytes | hHpSCs in canals of Hering | BTSC in peribiliary glands |
Nanog, OCT4 | - | - | + |
CXCR4 | - | - | + |
FoxA ½ | - | - | + |
PDX1, NGN3 | - | - | + |
AFP | - | + | + |
Sox 9/17 | - | + | + |
Prominin-1 (CD133) | - | + | + |
EpCAM | +/- | + | + |
NCAM | - | + | + |
Thy | - | + | + |
CK7/19 | + | + | + |
Secretin Receptor | + | - | - |
γGT | + | +/- | +/- |
Comparison of the phenotype among mature cholangiocytes, hepatic stem cells (hHpSCs) in canals of hering and biliary tree stem/progenitor cells (BTSC) in peribiliary glands. Mature cholangiocytes do not express markers of stem/progenitor cells. A complete study of the phenotype of cholangiocarcinoma considering these markers would indicate the probable cell of origin. AFP: α-fetoprotein; CD133: Prominin; CK: Cytokeratin; CXCR4: CXC-chemokine receptor 4; EpCAM: Epithelial cell adhesion molecule; FOXa2: Forkhead box a2; γGT: γ-glutamiltranspeptidasi; NCAM: Neural cell adhesion molecule; NGN3: Neurogenin 3; OCT4: Octamer-binding transcription factor 4 also known as POU5F1 (POU domain, class 5, transcription factor 1); PDX1: Pancreatic and duodenal homeobox 1; SOX: Sry-related HMG box.