Differential stromal and epithelial localization of cyclooxygenase-2 (COX-2) during colorectal tumorigenesis

被引:0
|
作者
Amoletti, JP
Upson, J
Babb, JS
Bellacosa, A
Watson, JC
机构
[1] Fox Chase Canc Ctr, Dept Human Genet, Philadelphia, PA 19111 USA
[2] Univ Alabama Birmingham, Dept Surg, Sect Surg Oncol, Birmingham, AL 35294 USA
[3] Fox Chase Canc Ctr, Dept Biostat, Philadelphia, PA 19111 USA
[4] Fox Chase Canc Ctr, Dept Surg Oncol, Philadelphia, PA 19111 USA
来源
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH | 2005年 / 24卷 / 02期
关键词
COX-2; protein; mRNA; colorectal cancer;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The purpose of the following study is to describe the localization of COX-2 protein and COX-2 mRNA during human colorectal tumorigenesis and to identify potential cellular targets for COX-2 inhibition in chemopreventive strategies. Immunohistochemistry with digital image analysis was used to determine COX-2 protein expression in histologic sections containing synchronous normal colorectal mucosa, adenomas and carcinomas, from 17 previously untreated patients. Epithelial and stromal COX-2 mRNA expression was analyzed by reverse transcription-polymerase chain reaction (RT-PCR), on laser-capture microdissected samples from the same histologies. The stromal compartment in normal colorectal mucosa and adenomas showed higher levels of COX-2 protein expression compared to colorectal carcinomas (p < .0001). Conversely, epithelial COX-2 protein was significantly increased only after development of the invasive phenotype (p < .0001). RT-PCR demonstrated higher stromal COX-2 mRNA expression compared to that within the epithelium for colorectal adenomas and carcinomas. In conclusion, stromal COX-2 may be the target for chemopreventive agents in the early stages of colorectal carcinogenesis.
引用
收藏
页码:279 / 287
页数:9
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