Development of extrahepatic bile ducts and mechanisms of tumorigenesis: Lessons from mouse models

Pathol Int. 2022 Dec;72(12):589-605. doi: 10.1111/pin.13287. Epub 2022 Nov 9.

Abstract

The biliary system is a highly branched tubular network consisting of intrahepatic bile ducts (IHBDs) and extrahepatic bile ducts (EHBDs). IHBDs are derived from hepatic progenitor cells, while EHBDs originate directly from the endoderm through a separate branching morphogenetic process. Traits that are important for cancer are often found to overlap in developmental and other processes. Therefore, it has been suggested that intrahepatic cholangiocarcinomas (iCCAs) and extrahepatic cholangiocarcinomas (eCCAs) have different developmental mechanisms. While much evidence is being gathered on the mechanism of iCCAs, the evidence for eCCA is still very limited. The main reason for this is that there are very few appropriate animal models for eCCA. We can gain important insights from these animal models, particularly genetically engineered mouse models (GEMMs). GEMMs are immunocompetent and mimic human CCA subtypes with a specific mutational pattern, allowing the development of precancerous lesions, that is, biliary intraepithelial neoplasia (BilIN) and intraductal papillary neoplasm of the bile duct (IPNB). This review provides a summary of the pathogenesis and mechanisms of eCCA that can be revealed by GEMMs. Furthermore, we discuss several clinical questions, such as whether BilIN and IPNB really become malignant, whether the peribiliary gland is the origin of eCCAs, and others.

Keywords: BilIN; IPNB; animal model; bile duct cancer; biliary tree; cholangiocarcinoma; extrahepatic duct; genetically engineered mouse model; peribiliary gland; precancerous lesion.

Publication types

  • Review

MeSH terms

  • Animals
  • Bile Duct Neoplasms* / pathology
  • Bile Ducts, Extrahepatic* / pathology
  • Bile Ducts, Intrahepatic / pathology
  • Bile Pigments
  • Cell Transformation, Neoplastic / genetics
  • Cell Transformation, Neoplastic / pathology
  • Cholangiocarcinoma* / pathology
  • Humans
  • Mice

Substances

  • Bile Pigments