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

被引:127
作者
Maitra, A
Ashfaq, R
Gunn, CR
Rahman, A
Yeo, CJ
Sohn, TA
Cameron, JL
Hruban, RH
Wilentz, RE
机构
[1] Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD 21205 USA
[2] Johns Hopkins Med Inst, Dept Oncol, Baltimore, MD 21205 USA
[3] Johns Hopkins Med Inst, Dept Surg, Baltimore, MD 21205 USA
[4] Univ Texas, SW Med Ctr, Dept Pathol, Dallas, TX USA
关键词
cyclooxygenase; 2; pancreatic adenocarcinoma; PanIN; pancreatic intraepithelial neoplasia; image analysis;
D O I
10.1309/TPG4-CK1C-9V8V-8AWC
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
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.
引用
收藏
页码:194 / 201
页数:8
相关论文
共 38 条
[1]   Neoplasms of the ampulla of Vater with concurrent pancreatic intraductal neoplasia: A histological and molecular study [J].
Agoff, SN ;
Crispin, DA ;
Bronner, MP ;
Dail, DH ;
Hawes, SE ;
Haggitt, RC .
MODERN PATHOLOGY, 2001, 14 (03) :139-146
[2]  
Bauer KD, 2000, CLIN CANCER RES, V6, P3552
[3]  
Bresalier R S, 2000, Gastroenterology, V119, P267
[4]  
Dannenberg AJ, 1999, SEMIN ONCOL, V26, P499
[5]   UP-REGULATION OF CYCLOOXYGENASE-2 GENE-EXPRESSION IN HUMAN COLORECTAL ADENOMAS AND ADENOCARCINOMAS [J].
EBERHART, CE ;
COFFEY, RJ ;
RADHIKA, A ;
GIARDIELLO, FM ;
FERRENBACH, S ;
DUBOIS, RN .
GASTROENTEROLOGY, 1994, 107 (04) :1183-1188
[6]   Biochemistry of cyclooxygenase (COX)-2 inhibitors and molecular pathology of COX-2 in neoplasia [J].
Fosslien, E .
CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES, 2000, 37 (05) :431-502
[7]   TREATMENT OF COLONIC AND RECTAL ADENOMAS WITH SULINDAC IN FAMILIAL ADENOMATOUS POLYPOSIS [J].
GIARDIELLO, FM ;
HAMILTON, SR ;
KRUSH, AJ ;
PIANTADOSI, S ;
HYLIND, LM ;
CELANO, P ;
BOOKER, SV ;
ROBINSON, CR ;
OFFERHAUS, GJA .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 328 (18) :1313-1316
[8]   Very high risk of cancer in familial Peutz-Jeghers syndrome [J].
Giardiello, FM ;
Brensinger, JD ;
Tersmette, AC ;
Goodman, SN ;
Petersen, GM ;
Booker, SV ;
Cruz-Correa, M ;
Offerhaus, JA .
GASTROENTEROLOGY, 2000, 119 (06) :1447-1453
[9]   BRCA2 is inactivated late in the development of pancreatic intraepithelial neoplasia -: Evidence and implications [J].
Goggins, M ;
Hruban, RH ;
Kern, SE .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 156 (05) :1767-1771
[10]  
Goggins M, 1996, CANCER RES, V56, P5360