大鼠混合反流模型中COX2、PCNA、Cyclin D1的表达
反流性食管炎(RE),,反流性食管炎(RE);Barrett食管(BE);食管腺癌(EAC);环氧合酶2(COX2);增殖细胞核抗原(PCNA);细胞周期蛋白D1(Cyclin,D1),大鼠混合反流模型中COX2、PCNA、CyclinD1的表达,1材料与方法,2结果,3讨论,参考文献
摘要:目的 探讨环氧合酶2(COX2)、增殖细胞核抗原(PCNA)及细胞周期蛋白D1(Cyclin D1)这3项指标在反流性食管炎的发生、发展及癌变过程中的变化情况。方法 健康SD大鼠54只,随机分为2组:反流模型组46只,正常对照组8只。分别观察反流模型组术后5、17、28、40周,正常对照组40周时食管黏膜的病理变化,检测COX2、PCNA、Cyclin D1的表达情况。结果 在反流性食管炎的发展过程中,COX2、PCNA、Cyclin D1从正常→反流性食管炎(RE)→Barrett食管(BE)→食管腺癌(EAC)的阳性表达率分别为0.0%、42.1%、73.7%、100.0%;0.0%、42.1%、63.2%、100.0%;12.5%、42.1%、63.2%、100.0%。COX2、PCNA、Cyclin D1的表达程度逐渐增强。RE、BE、EAC的表达明显高于正常对照(P<0.05),RE与BE、EAC间有显著性差异(P<0.05),BE和EAC间无统计学差异可能是EAC的例数较少。结论 在混合反流造成黏膜损伤形成RE的同时, COX2、PCNA和Cyclin D1的表达增强,并随病程的发展逐渐增强。说明COX2、PCNA和Cyclin D1基因的高表达参与了从RE→BE→EAC的发展过程,是BE、EAC发生、发展的早期分子事件。关键词:反流性食管炎(RE);Barrett食管(BE);食管腺癌(EAC);环氧合酶2(COX2);增殖细胞核抗原(PCNA);细胞周期蛋白D1(Cyclin D1)
The expression of COX2, PCNA and Cyclin D1 in the model of reflux esophagitis
Wang Tao, Gong Jun, Chen Qian, Wang Jinhai
(1. Department of Gastroenterology, Second Hospital of Xian Jiaotong University, Xian 710004;2. Department of Tumor Radiotherapy, First Hospital of Xian Jiaotong University, Xian 710061, China)
ABSTRACT: ObjectiveTo investigate the expression of COX2, PCNA and Cyclin D1 in the progress of reflux esophagitis. Methods A total of 54 SD rats were divided into two groups randomly model group were treated with esophagoduodenostomy; control group were normals. The lesions of esophageal mucosa were observed in the 5th, 17th, 28th, 40th week in model group and 40th week in control group, respectively. The changes of COX2, PCNA and Cyclin D1 were evaluated by immunoperoxidase staining in the progress of reflux esophagitis. Results The positive rates of COX2, PCNA and Cyclin D1 were 0.0%, 0.0% and 12.5% in normal respectively, and were 42.1%, 42.1% and 42.1% in RE respectively, 73.7%, 63.2% and 63.2% in BE, and 100.0%,100.0% and 100.0% in EAC, respectively. The expression of COX2, PCNA and Cyclin D1 increased gradually with the development of reflux esophagitis, and significant difference was found between RE, BE and EAC, no difference was found between BE and EAC. Conclusion In the progress of RE, COX2, PCNA and Cyclin D1 increased gradually. ......
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