Comparative evaluation of cancer stem cell markers in normal pancreas and pancreatic ductal adenocarcinoma

• DOI: 10.3892/or.2011.1461
• Publication Date: 2011-09-14T08:50:36Z
• Authors: Graziella Bellone
• Keywords: Adult; Male; 0301 basic medicine; Middle Aged; Immunohistochemistry; ABCG2; Aldehyde dehydrogenase; Cancer stem cells; CD133; Jagged; Nestin; Notch; Pancreatic adenocarcinoma; Tissue microarray; Adult; Aged; Biomarkers, Tumor; Carcinoma, Pancreatic Ductal; Female; Humans; Immunohistochemistry; Male; Middle Aged; Neoplasm Grading; Neoplasm Staging; Neoplastic Stem Cells; Pancreas; Pancreatic Neoplasms; Cancer Research; Oncology; 3. Good health; Pancreatic Neoplasms; 03 medical and health sciences; Biomarkers, Tumor; Neoplastic Stem Cells; Humans; Female; Neoplasm Grading; Pancreas; Aged; Carcinoma, Pancreatic Ductal; Neoplasm Staging

Chemoresistance and self-renewal of cancer stem cells (CSC), found in many tumors including pancreatic ductal adenocarcinoma (PDAC), are believed to underlie tumor mass regrowth. The distribution of cells carrying the putative stem-cell markers CD133, Nestin, Notch1-4, Jagged1 and 2, ABCG2 and aldehyde dehydrogenase (ALDH1) was assessed immunohistochemically using PDAC and normal pancreas tissue microarrays. The immunoreactivity was semi-quantitatively graded against the normal pancreas and was correlated with the differentiation grade and disease stage. No statistical significant differences were found between normal pancreas and PDAC in the expression of Nestin, Notch1, 3 and 4, ABCG2 or ALDH1. Notch2 and Jagged1 and 2 expression were increased in PDAC. CD133-positive cells were above-normal in PDAC, but the difference was not statistically significant. Nestin, Notch1-4, Jagged1, ABCG2 and ALDH1 immunostaining scores were not correlated with tumor grade or disease stage. CD133 and Notch2 expression was significantly inversely correlated with tumor grade, but not disease stage. Notch3 immunostaining positively correlated with tumor stage, but not with differentiation grade. Jagged2 protein expression correlated inversely with disease stage, but not with tumor grade. From the clinical standpoint, improved delineation of the tumor CSC signature, putatively responsible for tumor initiation and recurrence after initial response to chemotherapy, may offer novel therapeutic targets for this highly lethal cancer.