Where and when does pancreatic carcinoma start?

Med Klin (Munich). 2004 Apr 15;99(4):191-5. doi: 10.1007/s00063-004-1028-3.

Abstract

The phenotypic classification of pancreatic neoplasms is based on their cellular lineage. Thus, tumors with a ductal, acinar and endocrine phenotype can be distinguished. Most pancreatic neoplasms show a ductal phenotype and can be classified as ductal adenocarcinomas. Less common tumors with a ductal phenotype are the variants of ductal adenocarcinoma, intraductal papillary-mucinous neoplasm (including colloid carcinoma), mucinous cystic neoplasm, medullary carcinoma and other rare tumors. Ductal adenocarcinomas most likely develop on the basis of ductal proliferative lesions arising in the pancreatic duct system. A recently adopted classification system for these lesions distinguishes between three grades of pancreatic intraepithelial neoplasia (PanIN). Molecular studies revealed that PanIN-2 and PanIN-3 lesions represent a distinct step toward invasive carcinoma.

MeSH terms

  • Carcinoma in Situ / genetics
  • Carcinoma in Situ / pathology*
  • Carcinoma, Pancreatic Ductal / genetics
  • Carcinoma, Pancreatic Ductal / pathology*
  • Cell Transformation, Neoplastic / genetics
  • Cell Transformation, Neoplastic / pathology*
  • Disease Progression
  • Gene Expression Regulation, Neoplastic / physiology
  • Genes, Tumor Suppressor
  • Genes, ras / genetics
  • Humans
  • Neoplasm Invasiveness / genetics
  • Neoplasm Invasiveness / pathology
  • Neoplasm Staging
  • Pancreas / pathology
  • Pancreatic Ducts / pathology
  • Pancreatic Neoplasms / genetics
  • Pancreatic Neoplasms / pathology*
  • Phenotype
  • Thyroid Hormone Receptors beta / genetics

Substances

  • Thyroid Hormone Receptors beta