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作 者:张玉洁 杜强 朱丽娟[2] 张艳[3] 李晓梅[2] 蒲红伟[3] 陈晓[3]
机构地区:[1]克孜勒苏自治州人民医院病理科,新疆维吾尔自治区阿图什市845350 [2]新疆医科大学厚博学院病理学教研室,新疆维吾尔自治区乌鲁木齐市830011 [3]新疆医科大学基础医学院病理学教研室,新疆维吾尔自治区乌鲁木齐市830011
出 处:《世界华人消化杂志》2014年第30期4609-4614,共6页World Chinese Journal of Digestology
基 金:国家自然科学基金资助项目;No.81360303~~
摘 要:目的:研究食管鳞状细胞癌(esophageal squamous cell carcinoma,ESCC)组织中S100A11、14-3-3的表达及其临床意义.方法:应用免疫组织化学SP法检测68例ESCC组织和48例癌旁切端正常食管组织,观察S100A11、14-3-3的表达,并应用统计学方法分析其表达与临床病理学指标的意义.结果:(1)ESCC组织中S100A11、14-3-3蛋白的阳性表达率分别为:55.9%(38/68)、69.1%(47/68).正常食管组织中阳性表达率分别为:25.0%(12/48)、33.3%(16/48),经比较差异均有统计学意义(P<0.05);(2)ESCC组织中S100A11在不同性别、年龄、民族、肿瘤大小及不同浸润深度组之间的表达差异无统计学意义(P>0.05);在不同分化程度、有无淋巴结转移及不同临床分期组之间的表达差异有统计学意义(P<0.05);(3)ESCC组织中14-3-3在不同性别、年龄、民族及不同肿瘤大小组之间的表达差异无统计学意义(P>0.05);在不同分化程度、不同浸润深度、有无淋巴结转移及不同临床分期组之间的表达差异有统计学意义(P<0.05).结论:提示S100A11、14-3-3在ESCC的发生和发展中可能起到一定作用.S100A11、14-3-3在不同分化程度、有无淋巴结转移及不同临床分期组之间的表达均有显著差异,提示S100A11、14-3-3可能对ESCC恶性程度判断有一定的指导意义.AIM: To determine the correlation between invasion, migration and prognosis of esophageal squamous cell carcinoma (ESCC) and expression of S100A11 and 14-3-3 proteins. METHODS: Sixty-eight previously untreated pa-tients who underwent surgical excision of ESCC were included. The expression of S100All and 14-3-3 proteins was examined immunohistochemically in formalin-fixed paraffin-embedded primary tissue specimens. The relationships between the expression of S100All and 14-3-3 proteins, the clinicopathologic features of ESCC, and the survival rate of ESCC patients were analyzed. The correlation between S100A11 and 14-3-3 protein expression in ESCC was also analyzed. RESULTS: The positive rates of S100A11 and 14-3-3 protein expression were significantly higher in ESCC than in normal esophageal tissues (55.9% vs 25.0%, 69.1% vs 33.3%, P 〈 0.05). S100A11 expression showed no significant correlation with gender, age, ethnicity, tumor size or infiltration depth (P 〉 0.05), but was significantly correlated with degree of differentiation, lymph node metastasis and clinical stage (P 〈 0.05). 14-3-3 expression showed no significant correlation with gender, age, ethnicity, or tumor size (P 〉 0.05), but was significantly correlated with degree of differentiation, depth of infiltration, lymph node metastasis and clinical stage (P 〈 0.05). CONCLUSION: S100A11 and 14-3-3 may play a role in the occurrence and development of ESCC. The expression of S100A11 and14-3-3 is significantly related to tumor differentiation, lymph node metastasis and clinical stage, and they may be used to assess the malignant degree of ESCC.
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