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作 者:王渝[1] 柯昌庶[2] 赵秋[1] 马松林[1] 龚勇[1] 杨芳[1]
机构地区:[1]华中科技大学同济医学院附属同济医院消化内科,湖北省武汉市430030 [2]华中科技大学同济医学院附属同济医院病理科,湖北省武汉市430030
出 处:《世界华人消化杂志》2007年第4期403-407,共5页World Chinese Journal of Digestology
摘 要:目的:研究E-cadherin,β-catenin,Cyclin D1在胃腺癌组织中的表达,探讨三者的表达及临床病理意义.方法:采用免疫组织化学SP法检测73例胃腺癌组织及18例正常胃黏膜组织中E-cadherin,β-catenin,Cyclin D1蛋白的表达.结果:正常胃黏膜组织中E-cadherin和β-catenin均呈清晰的棕褐色染色在上皮细胞细胞膜.E-cadherin和β-catenin在胃癌细胞中出现细胞质和/或细胞核异常染色,其异常表达率分别为63.01%(46/73)和56.16%(41/73),且两者的异常表达与胃腺癌的分化程度、TNM分期、浸润深度及淋巴结转移相关.与患者的性别、年龄、肿瘤大小无关.胃腺癌中E-cadherin和β-catenin表达密切相关.Cyclin D1在胃腺癌组织中的阳性表达率为67.12%(49/73),明显高于其在正常胃黏膜组织中的表达(0%,0/18),且与胃腺癌的分化程度和淋巴结转移相关.E-cadherin和β-catenin在胃癌中的异常表达与Cyclin D1的过表达呈显著的正相关(r=0.249,r=0.376,P<0.05).结论:胃腺癌中存在E-cadherin和β-catenin基因的失活及蛋白表达下调.E-cadherin和β-catcnin的异常表达可能通过促使或激活Cyclin D1的过表达而参与胃癌的发生和发展.AIM: To investigate the expression of E-cadherin, β-catenin and Cyclin D1 and their relationships and clinical pathological features in gastric adenocarcinoma. METHODS: Immunohistochemical SP method was used to determine the expression of E-cadherin, β-catenin and Cyclin D1 protein in 73 cases of gastric adenocarcinoma tissues and 18 cases of normal gastric mucosal tissues. RESULTS: Positive staining for E-cadherin and β-catenin was observed on the cellular membrane of epithelial cells in normal gastric mucosal tissues. The aberrant expression of E-cadherin and β-catenin were observed in thecytoplasm and/or cellular nucleus of gastric cancer cells. The aberrant expression rates of E-cadherin and β-catenin were 63.01% (46/73) and 56.16% (41/73) in gastric adenocarcinoma, respectively, which were associated with the differentiation degree, TNM stages, depth of infiltration and lymph node metastasis, but not with the gender, age and tumor size. There was a significant correlation between E-cadherin and β-catenin expression in gastric adenocarcinoma. The positive rate of Cyclin D1 expression was 67.12% (49/73) in gastric adenocarcinoma, notably higher than that in normal gastric tissues (0/18, P 〈 0.01), and it was correlated with the differentiation degree and lymph node metastasis. The aberrant expression of E-cadherin and β-catenin were positively correlated with the high expression of Cyclin D1 gastric carcinoma (r = 0.249, 0.376, both P 〈 0.05). CONCLUSION: Down-regulated expression of E-cadherin and β-catenin exist in gastric carcinoma, which may promote the pathogenesis and development of carcinoma by activation of Cyclin D1.
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