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作 者:杨东霞[1] 韩艳春[1] 刘鲁英[1] 于宁[1] 王霞[1] 时彦[1]
机构地区:[1]滨州医学院病理学教研室,山东烟台264003
出 处:《癌症》2009年第7期762-767,共6页Chinese Journal of Cancer
摘 要:背景与目的:血管内皮生长因子(vascularendothelialgrowthfactor,VEGF)促进肿瘤血管生成的作用与Ets家族有关,Ets家族中对Elf-1的研究较少。本研究检测非小细胞肺癌(non-smallcelllungcancer,NSCLC)组织中转录因子Elf-1和VEGF的表达,探讨其与NSCLC临床病理特征的关系。方法:制备含69例NSCLC组织和6例正常肺组织的组织芯片,采用免疫组化PowerVision-9000法检测Elf-1和VEGF蛋白的表达水平。结果:Elf-1和VEGF在正常肺组织中的表达均为阴性,在NSCLC组织中表达的阳性率分别为72.46%和63.77%,其表达水平与肿瘤细胞分化程度、淋巴结转移、临床分期和术后生存期有关(P<0.01)。Kaplan-Meier生存分析表明二者的过表达均与患者的生存率有关,阳性表达的患者生存率明显低于阴性者(P<0.01)。在NSCLC中,Elf-1的表达与VEGF的表达呈正相关(r=0.702,P<0.01)。结论:Elf-1和VEGF在NSCLC组织中的过表达与肿瘤的分化程度、转移和预后均有关,联合检测二者的表达水平可作为判定NSCLC恶性生物学行为的参考指标。Background and Objective: The roles of vascular endothelial growth factor (VEGF) in tumor angiogenesis is related with Ets family. Elf-1, a member of Ets family, has seldom been studied. This study aimed to investigate the expression of Elf-1 and VEGF in non-small cell lung cancer (NSCLC), and explore their correlations to clinicopathologic features of NSCLC. Methods: Tissue microarray containing 69 specimens of NSCLC and six specimens of normal lung tissues was constructed. The expression of Elf-1 and VEGF was detected by PowerVisionTU-9000 immunohistochemistry. Results= Elf-1 and VEGF were not detected in all normal tissues; the positive rates of Elf-1 and VFGF were 72.46% and 63.77% in NSCLC, respectively. The expression levels of both Elf-1 and VEGF were significantly related with tumor differentiation, lymphatic metastasis, clinical stage, and postoperative survival time (all P 〈 0.01 ). Overexpression of them was related with poor prognosis: the survival rates were significantly lower in positive patients than in negative patients (both P 〈 0.01 ). Elf-1 expression was positively correlated to VEGF expression (r = 0.702, P 〈 0.01 ). Conclusions: The expression of Elf-1 and VEGF in NSCLC is related to differentiation, lymphatic metastasis, clinical stage and prognosis. Detecting their expression in combination can help to predict the malignant behavior of NSCLC.
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