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机构地区:[1]中国医科大学附属第四医院生物治疗科,辽宁沈阳110032
出 处:《现代肿瘤医学》2015年第7期974-977,共4页Journal of Modern Oncology
基 金:辽宁省自然科学基金资助项目(编号:201102266)
摘 要:目的:探讨NIK和IKKβ连接蛋白(NIK and IKKβbinding protein,NIBP)在结肠癌组织中的表达及其与临床病理和预后之间的关系。方法:应用免疫组织化学染色法检测组织芯片中133例结肠癌和92例相匹配的癌旁正常结肠组织中NIBP蛋白的表达水平。结果:结肠癌组织中肿瘤细胞NIBP蛋白表达水平明显高于癌旁正常结肠组织上皮细胞(P=0.000)。NIBP蛋白表达水平与临床分期显著相关(P=0.044),与性别、年龄、肿瘤侵袭深度、淋巴结转移、远处转移、组织学类型、组织学分级无关。单因素生存分析显示NIBP蛋白高水平表达者较低水平表达者总生存期明显延长(P=0.006),多因素分析结果表明NIBP蛋白表达水平是结肠癌患者独立的预后因素(HR=0.461,95%CI=0.229-0.925,P=0.029)。结论:NIBP可能参与结肠癌的发生发展,可能是预测结肠癌预后的新的生物学标志物。Objective: To measure the expression of NIK and IKKβ binding protein( NIBP) in colon cancer and to determine its association with the clinicopathological characteristics and prognosis of patients with colon cancer.Methods: Immunohistochemistry for NIBP was done on tissue microarray containing 133 cores of colon cancer and 92 cores of normal colon tissues matched to tumor sections. Results: Tumor cells NIBP expression was significantly increased compared with normal colon epithelium cells( P = 0. 000). Tumor cells NIBP expression was found to be significantly correlated with clinical stage( P = 0. 044),but was unrelated to gender,age,deeper invasion,presence of lymph node metastases,distant metastasis,histology type and grade. Univariate factor analysis showed that high NIBP expression was significantly associated with prolonged overall survival compared to patients with low expression( P =0. 006). Cox multivariate modelling confirmed that high NIBP expression was an independent prognostic factor for colon cancer patients( HR = 0. 461,95% CI = 0. 229- 0. 925,P = 0. 029). Conclusion: NIBP is likely to play an important role in colon cancer tumorigenesis and progression. NIBP may be a novel prognostic marker for colon cancer.
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