COX-2 expression in sporadic colorectal adenomatous polyps is linked to adenoma characteristics

被引:22
作者
McLean, M. H. [1 ]
Murray, G. I. [2 ]
Fyfe, N. [2 ]
Hold, G. L. [1 ]
Mowat, N. A. G. [1 ]
El-Omar, E. M. [1 ]
机构
[1] Univ Aberdeen, Inst Med Sci, Dept Med & Therapeut, GI Res Grp, Aberdeen AB25 2ZD, Scotland
[2] Univ Aberdeen, Dept Pathol, Aberdeen AB25 2ZD, Scotland
关键词
adenoma; colorectal cancer; COX-2; dysplasia; hyperplastic polyp;
D O I
10.1111/j.1365-2559.2008.03038.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Aims: To assess cyclooxygenase-2 (COX-2) expression in sporadic colonic adenomas and to explore the association of COX-2 positivity with adenoma characteristics linked to increased risk of malignant transformation. Methods and results: COX-2 expression and localization were assessed in 64 colorectal adenomas and 35 paired adjacent normal colonic mucosal biopsy specimens. The number of adenoma specimens was then extended to include polyps exhibiting an increasing degree of epithelial dysplasia. Forty colonic hyperplastic polyps were also identified from the pathology diagnostic database and included in the analysis. Immunohistochemistry was performed with the Envision+(TM) peroxidase-linked biotin-free system incorporating a signal amplification step. There was a statistically significant increase in COX-2 expression in colonic polyps compared with paired adjacent normal mucosa, chi(2) = 40.1, P = 0.001. The probability of COX-2 expression increased along with increasing adenoma size and increasing degree of epithelial dysplasia. Fifty-five per cent of the hyperplastic polyp specimens expressed COX-2. Conclusions: This study associates COX-2 epithelial expression with a number of adenoma characteristics that convey an increased risk of malignant transformation. This is in keeping with a positive role for COX-2 in early colorectal carcinogenesis.
引用
收藏
页码:806 / 815
页数:10
相关论文
共 35 条
[1]   Size-dependent expression of cyclooxygenase-2 in sporadic colorectal adenomas relative to adenomas in patients with familial adenomatous polyposis [J].
Azumaya, M ;
Kobayashi, M ;
Ajioka, Y ;
Honma, T ;
Suzuki, Y ;
Takeuchi, M ;
Narisawa, R ;
Asakura, H .
PATHOLOGY INTERNATIONAL, 2002, 52 (04) :272-276
[2]   A randomized trial of aspirin to prevent colorectal adenomas [J].
Baron, JA ;
Cole, BF ;
Sandler, RS ;
Haile, RW ;
Ahnen, D ;
Bresalier, R ;
McKeown-Eyssen, G ;
Summers, RW ;
Rothstein, R ;
Burke, CA ;
Snover, DC ;
Church, TR ;
Allen, JI ;
Beach, M ;
Beck, GJ ;
Bond, JH ;
Byers, T ;
Greenberg, ER ;
Mandel, JS ;
Marcon, N ;
Mott, LA ;
Pearson, L ;
Saibil, F ;
van Stolk, RU .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (10) :891-899
[3]  
Boolbol SK, 1996, CANCER RES, V56, P2556
[4]   Localization of cyclooxygenase-2 in human sporadic colorectal adenomas [J].
Chapple, KS ;
Cartwright, EJ ;
Hawcroft, G ;
Tisbury, A ;
Bonifer, C ;
Scott, N ;
Windsor, ACJ ;
Guillou, PJ ;
Markham, AF ;
Coletta, PL ;
Hull, MA .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 156 (02) :545-553
[5]  
Colucci Philomena M, 2003, Clin Med Res, V1, P261
[6]   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
[7]  
Einspahr JG, 2003, CANCER RES, V63, P3891
[8]   Human colorectal adenomas demonstrate a size-dependent increase in epithelial cyclooxygenase-2 expression [J].
Elder, DJE ;
Baker, JA ;
Banu, NA ;
Moorghen, M ;
Paraskeva, C .
JOURNAL OF PATHOLOGY, 2002, 198 (04) :428-434
[9]   A GENETIC MODEL FOR COLORECTAL TUMORIGENESIS [J].
FEARON, ER ;
VOGELSTEIN, B .
CELL, 1990, 61 (05) :759-767
[10]   ASPIRIN AND THE RISK OF COLORECTAL-CANCER IN WOMEN [J].
GIOVANNUCCI, E ;
EGAN, KM ;
HUNTER, DJ ;
STAMPFER, MJ ;
COLDITZ, GA ;
WILLETT, WC ;
SPEIZER, FE .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (10) :609-614