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作 者:李秀娟[1] 聂永梅[2] 张志强[3] 张桂英[4] 李茂玉[5] 宋娜[6] 苏丽萍[6] 倪自翔[6]
机构地区:[1]新疆医科大学基础医学院病理生理学教研室,乌鲁木齐市830011 [2]新疆医科大学基础医学院生理学教研室 [3]新疆医科大学第一附属医院消化科 [4]中南大学湘雅医院消化科 [5]中南大学湘雅医院卫生部蛋白质组学重点实验室 [6]新疆医科大学基础医学院
出 处:《中国肿瘤临床》2012年第16期1188-1191,共4页Chinese Journal of Clinical Oncology
基 金:国家自然科学基金(编号:81001101);新疆维吾尔自治区自然科学基金(编号:2010211B20);新疆维吾尔自治区高校科研计划青年教师科研启动基金(编号:XJEDU2010S24);自治区卫生厅青年科技人才专项科研基金项目(编号:2009Y06)资助~~
摘 要:目的:探讨胃癌(GC)中S100A9的表达及临床病理意义。方法:蛋白质组织学定量鉴定GC和癌旁胃黏膜(GM)组织的差异表达蛋白质;Western-blot验证蛋白S100A9的表达;免疫组织化学检测S100A9蛋白在GC、GM和原发性胃癌转移的淋巴结(LN)的表达;分析S100A9表达与GC临床病理参数的关系。结果:蛋白质组织学筛选的78个差异蛋白中,S100A9表达在GC中较正常GM中明显上调(1∶0.09),Western-blot验证S100A9蛋白在GC表达上调(P<0.01);免疫组织化学显示:70例正常GM中S100A9阳性表达23例(32.86%);118例GC中S100A9阳性表达72例(61.02%);35例LN中S100A9阳性表达29例(82.86%),与正常GM相比,GC和LN中S100A9的表达明显升高(P<0.01);S100A9在LN的GC中上调(P<0.05);S100A9表达与GC的淋巴结转移、分化程度、浸润深度和TNM分期相关(P<0.01或P<0.05),而与患者的年龄和性别无关(P>0.05)。结论:S100A9高表达与GC发生发展、侵袭转移有关,可能是GC的一个促癌因子。Objective: This study aims to investigate the expression and clinicopathologic significance of the S 100A9 protein in gastric cancer ( GC ). Methods: Differential expression of proteins between GC and paraneoplastic gastric mucosa ( GM ) tissues was quantitatively determined using proteomics. The S100A9 protein level was examined using western blot analysis. The S 100A9 protein expression in GC, GM, and lymph node ( LN ) of primarily gastric carcinomatous metastasis was determined using immunohistochemistry ( IHC ). The relationship between S100A9 protein expression and the clinicopathologic parameters of GC was analyzed. Results: Among the 78 differential proteins identified through proteomics, S 100A9 protein expression was clearly upregulated in GC compared with the GM ( 1:0.09 ), which was confirmed through western blot analysis ( P 〈 0.01 ). The IHC assay showed the positive expression of 23 S100A9 proteins ( 32.86 % ) among 70 normal GC samples, 72 ( 61.02 % ) among 118 GM samples, and 29 ( 82.86 % ) among 35 LN samples. Compared with GM, S100A9 expression was significantly increased in GC and LN ( P 〈 0.01 ). S100A9 expression was upregulated in LN compared with GC ( P 〈 0.05 ). The S100A9 expression level in GC was correlated with LN metastasis, histologic differentiation, depth of invasion, and TNM stage ( P 〈 0.01 or P 〈 0.05 ), but not correlated with the patient age and gender ( P 〉 0.05 ). Conclusion: S 100A9 protein overexpression is correlated with GC carcinogenesis, invasion, and metastasis and it may promote GC.
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