4.3 Article

Cyclooxygenase 2 expression in pancreatic adenocarcinoma and pancreatic intraepithelial neoplasia - An immunohistochemical analysis with automated cellular imaging

Journal

AMERICAN JOURNAL OF CLINICAL PATHOLOGY
Volume 118, Issue 2, Pages 194-201

Publisher

AMER SOC CLINICAL PATHOLOGY
DOI: 10.1309/TPG4-CK1C-9V8V-8AWC

Keywords

cyclooxygenase 2; pancreatic adenocarcinoma; PanIN; pancreatic intraepithelial neoplasia; image analysis

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Funding

  1. NCI NIH HHS [P50-CA62924] Funding Source: Medline

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We immunohistochemically examined material from 36 pancreata (adenocarcinomas, 30 lesions; pancreatic intraepithelial neoplasia [PanIN], 65; normal pancreatic ducts, 30)for cyclooxygenase 2 (COX-2) with an automated platform. We analyzed 7 to 10 discrete foci and generated an average percentage of positive cells and average staining intensity for each lesion. These 2 values were then multiplied to create an overall HistoScore for each lesion. COX-2 demonstrated considerable heterogeneity of expression between and within cases. The overall average percentage of positive cells in adenocarcinomas was 47.3%; in PanINs, 36.3%; and in normal ducts, 19.2%. COX-2 was expressed in more than 20% of cells in 23 adenocarcinomas (77%), 42 PanINs (65%), and 12 normal ducts (40%). The overall average HistoScore for adenocarcinomas was 6.1; for PanINs, 5.4; and for normal ducts, 3.5. Significant differences in COX-2 expression were demonstrable in adenocarcinomas vs normal ducts, PanINs vs normal ducts, and AMIN 213 vs PanIN 1a/1b. In general, the pattern of COX-2 expression increased from normal to PanIN to adenocarcinoma. The up-regulation of COX-2 in a subset of noninvasive precursor lesions makes it a potential target for chemoprevention with selective COX-2 inhibitors.

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