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环氧化酶-2在中国食管鳞状细胞癌中过度表达,并与核因子-κB相关:一项免疫组织化学研究。

Cyclooxygenase-2 is over-expressed in Chinese esophageal squamous cell carcinoma, and correlated with NF-kappaB: an immunohistochemical study.

作者信息

Yang Guang-Zhi, Li Li, Ding Hua-Ye, Zhou Jin-Song

机构信息

Department of Pathology, The General Hospital of Beijing Military Command, Beijing 100700, People's Republic of China.

出版信息

Exp Mol Pathol. 2005 Dec;79(3):214-8. doi: 10.1016/j.yexmp.2005.09.002. Epub 2005 Oct 3.

DOI:10.1016/j.yexmp.2005.09.002
PMID:16202995
Abstract

BACKGROUND

Cyclooxygenase-2 (COX-2), the inducible isoform of the key enzyme in the synthesis of prostaglandins, has been found to be over-expressed in several human cancers. The aim of the present study was to investigate immunohistochemical expression of COX-2 in esophageal squamous cell carcinoma (SCC) and relationship with clinicopathological parameters and NF-kappaB.

METHODS

Expression of COX-2 and NF-kappaB was investigated in 69 cases of esophageal SCC by immunohistochemistry and the correlation of COX-2 expression with clinicopathological features and NF-kappaB staining was examined.

RESULTS

Thirty-one esophageal SCC (31/69, 44.9%) had positive expression of COX-2. COX-2 was expressed significantly higher in well-differentiated tumors (16/23, 69.6%) than that in moderate (13/34, 38.2%) and poor (2/12, 16.7%) differentiation (P = 0.034). COX-2 expression was increasingly progressive with the advance of the clinical stages significantly (P = 0.045). The correlation between COX-2 (47/99, 47.5%) and NF-kappaB/p50 (54/99, 54.5%) immunostaining was statistically significant (P = 0.030).

CONCLUSIONS

COX-2 is over-expressed in esophageal SCC, especially in a well differentiation, correlated with tumor progression, and possibly regulated by NF-kappaB.

摘要

背景

环氧化酶-2(COX-2)是前列腺素合成关键酶的诱导型同工酶,已发现在多种人类癌症中过度表达。本研究旨在探讨COX-2在食管鳞状细胞癌(SCC)中的免疫组化表达及其与临床病理参数和核因子κB(NF-κB)的关系。

方法

采用免疫组化法检测69例食管SCC中COX-2和NF-κB的表达,并分析COX-2表达与临床病理特征及NF-κB染色的相关性。

结果

31例食管SCC(31/69,44.9%)COX-2呈阳性表达。COX-2在高分化肿瘤(16/23,69.6%)中的表达明显高于中分化(13/34,38.2%)和低分化(2/12,16.7%)肿瘤(P = 0.034)。COX-2表达随临床分期进展呈逐渐升高趋势,差异有统计学意义(P = 0.045)。COX-2(47/99,47.5%)与NF-κB/p50(54/99,54.5%)免疫染色的相关性具有统计学意义(P = 0.030)。

结论

COX-2在食管SCC中过度表达,尤其是在高分化肿瘤中,与肿瘤进展相关,可能受NF-κB调控。

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