Result: The positive rate of COX - 2 protein expression was 61.67 % in NPC tissues.

结果: COX -2 在NPC中 总的阳性表达率为61.67%.

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COX - 2 can become assistant biology index of estimating malignancy.

COX -2 可以作为判断脑胶质瘤恶性度的辅助生物学指标.

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Cox - 2 inhibitor may be a promising target for tumor chemoprevention and treatment.

Cox -2 选择性抑制剂有望成为NPC防治 的新靶点.

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Results: 200 μ M DCA induced cell proliferation and COX - 2 mRNA transcription.

结果: 200μMDCA可以 促进HT-29 细胞的增殖,并诱导COX -2 mRNA的转录、COX-2蛋白的表达及PGE2的合成.

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DCA up - regulated the expression of AP - l ( c - Jun c - Fos ) and COX - 2 in a dose dependent manner.

DCA能上调AP -1 ( c -Jun 、c-Fos ) 蛋白及COX -2 蛋白表达,呈浓度依赖性.

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Conclusion The high expressions of COX - 2 , VEGF in PCa may be related to tumor pathological grade.

结论COX -2 、 VEGF在前列腺癌中均为高表达,且与肿瘤的Gleason评分密切相关.

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Now, COX - 2 inhibitors are used to clinical practice gradually and they usually combine with other medicines.

目前, COX -2 抑制剂逐渐应用于临床实践,主要是与其他药物联合应用.

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COX - 2 expression was positively correlated to both p - Stat 3 expression and p - Stat 5 expression in ESCC.

COX -2 、p-Stat3及p-Stat5三者的表达之间呈正相关.

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COX - 2 was selectively expressed in some BE epithelium, but not in SRE and nomal esophageal epithelium.

COX - 2特异地表达于部分BE上皮, 在SRE及正常食管上皮中不表达.

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COX - 2 and COX - 2 inhibitor, where are we? where do we go?

环氧化酶 -2 及其抑制剂, 现在何处? 又应走向何方?

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Conclusions: 1 There is overexpression of COX - 2 in PC - 3 m cell line as in PC - 3 cell line.

结论: l同PC上细胞系一样,PC上m细胞系中存在 COX1mRNA 及蛋白质表达.

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The positive expression of COX - 2 and MMP - 2 was significantly higher in G ? 3 than in G ? 1 adenocarcinoma ( P & lt; 0.05 ).

COX2和 MMP2 在子宫颈腺癌的病理分级中, G3 组阳性表达率均明显高于G1组 ( P & lt; 0.05 ).

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