COX-2 expression of ampullary carcinoma:: correlation with different histotypes and clinicopathological parameters

被引:20
|
作者
Perrone, Giuseppe
Santini, Daniele
Zagami, Mariagiovanna
Vincenzi, Bruno
Verzi, Alfio
Morini, Sergio
Borzomati, Domenico
Coppola, Roberto
Antinori, Armando
Magistrelli, Paolo
Tonini, Giuseppe
Rabitti, Carla
机构
[1] Univ Rome, Oncol Unit, I-00155 Rome, Italy
[2] Univ Rome, Dept Biomed Res, I-00155 Rome, Italy
[3] Univ Rome, Dept Gen Surg, I-00155 Rome, Italy
[4] Univ Sacred Heart, Dept Gen Surg, I-00168 Rome, Italy
关键词
vater; ampulla; cancer; histotype; COX-2;
D O I
10.1007/s00428-006-0255-9
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Epidemiological studies suggest that regular intake of nonsteroidal anti-inflammatory drugs (NSAIDs) are associated with reduced incidence of gastrointestinal cancer. Several lines of evidence indicate that the antineoplastic effect of NSAIDs is attributable to COX-2 inhibition. The aim of our study was to assess COX-2 expression in a series of primary untreated ampullary carcinomas and its possible correlation with clinicopathological parameters. In the present study, 45 surgical specimens of invasive ampullary carcinomas were histologically classified into pancreaticobiliary, intestinal, and unusual types. COX-2 expression by immunohistochemical method was analyzed. High COX-2 expression was detected in 35 (77.8%) ampullary carcinomas. Among these, 20/21 (95.2%) were classified as intestinal, 9/18 (50%) pancreaticobiliary, and 6/6 (100%) unusual type. A significant statistical difference in terms of COX-2 expression was found between pancreaticobiliary vs intestinal type (P = 0.002). Furthermore, a negative significant statistical correlation was found between T factor and COX-2 expression (P = 0.047). The different COX-2 expression among histopathological types supports the concept of histogenetical difference of ampullary carcinomas. Furthermore, the high rate of COX-2 expression in the intestinal subtype of ampullary carcinoma may represent the rational for a histotype-tailored therapy targeting COX-2.
引用
收藏
页码:334 / 340
页数:7
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