CD117 Is a Specific Marker of Intraductal Papillary Mucinous Neoplasms (IPMN) of the Pancreas, Oncocytic Subtype

Int J Mol Sci. 2020 Aug 12;21(16):5794. doi: 10.3390/ijms21165794.

Abstract

The intraductal oncocytic papillary neoplasm (IOPN) of the pancreas has been recognized by WHO classification as a unique intraductal papillary mucinous neoplasm (IPMN) category. IOPN is composed of oxyphil cells, usually expressing MUC5AC, MUC6, and Hep Par-1, and harboring PRKACA/B fusion genes as their genetic hallmark. Although IOPNs are associated with an infiltrative adenocarcinoma in up to 30% of cases, the survival rate after surgical resection approaches 100%. This highlights the importance of the correct IOPN diagnosis, above all in cases with an associated invasive component. In this study, the immunohistochemical expression of CD117 was investigated in 111 IPMNs, including 17 oncocytic, 45 gastric, 20 pancreatico-biliary, and 29 intestinal IPMNs. We also tested the expression of MUC5AC, MUC6, and Hep Par-1 in the IOPN cohort. CD117 positivity was significantly more frequent in IOPNs compared to the other IPMN subtypes (p < 0.0001). Furthermore, within IOPN, a lower or absent CD117, MUC5AC, MUC6, and Hep Par-1 expression tended to be associated with the presence of an infiltrative component. Our findings shed light into the biology of these complex lesions, which are confirmed to be a distinctive IPMN subtype; notably, CD117 emerged as a potential, additional tool in the differential diagnosis of IPMNs.

Keywords: IOPN; IPMN; c-kit; intraductal; oncocytic; pancreas.

MeSH terms

  • Adenocarcinoma, Mucinous / metabolism
  • Adenocarcinoma, Mucinous / pathology*
  • Biomarkers, Tumor / metabolism*
  • Carcinoma, Papillary / metabolism
  • Carcinoma, Papillary / pathology*
  • Cell Line, Tumor
  • Cohort Studies
  • Humans
  • Mucins / metabolism
  • Oxyphil Cells / pathology*
  • Pancreatic Intraductal Neoplasms / metabolism
  • Pancreatic Intraductal Neoplasms / pathology*
  • Proto-Oncogene Proteins c-kit / metabolism*

Substances

  • Biomarkers, Tumor
  • Mucins
  • Proto-Oncogene Proteins c-kit