首页> 美国卫生研究院文献>Oncology Letters >Aurora-A is an efficient marker for predicting poor prognosis in human nasopharyngeal carcinoma with aggressive local invasion: 208 cases with a 10-year follow-up from a single institution
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Aurora-A is an efficient marker for predicting poor prognosis in human nasopharyngeal carcinoma with aggressive local invasion: 208 cases with a 10-year follow-up from a single institution

机译:Aurora-A是预测具有侵略性局部侵袭的人类鼻咽癌预后不良的有效标志物:208例病例由一家机构进行了为期10年的随访

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摘要

Aurora-A kinase (Aur-A), a member of a family of mitotic serine/threonine kinases, is known to be amplified in epithelial malignancies. In this study, we focused our investigation on Aur-A expression and its prognostic significance in nasopharyngeal carcinoma (NPC). Immunohistochemical staining for Aur-A was performed on the paraffin sections of 208 patients with NPC. Data were subjected to statistical analysis with respect to clinicopathological variables, overall survival and disease-free survival. An immunohistochemical analysis showed that Aur-A was highly expressed in 132 (63.5%) of the 208 NPC tissues examined. Aur-A expression was significantly correlated with T classification (P=0.012), clinical stage (P=0.003) and skull base invasion (P=0.003). Statistical analysis showed that Aur-A expression was inversely correlated with the 10-year overall and disease-free survival rates of NPC patients. Results of the multivariate analysis revealed that Aur-A expression was an independent prognostic indicator for patient survival. More significantly, Aur-A was found to be a marker for poor survival, which was mainly attributed to its high expression in the subgroup of T4 tumor classification with aggressive local invasion. These results indicated that Aur-A expression is inversely correlated with survival and directly correlated with the malignant status of NPC. Therefore, Aur-A may serve as a potential biological marker for poor prognosis in the T4 subgroup of patients.
机译:已知Aurora-A激酶(Aur-A)是有丝分裂丝氨酸/苏氨酸激酶家族的成员,在上皮恶性肿瘤中会扩增。在这项研究中,我们将研究重点放在Aur-A表达及其在鼻咽癌(NPC)中的预后意义上。对208例NPC患者的石蜡切片进行了Aur-A的免疫组织化学染色。对数据进行临床病理变量,总体生存和无病生存的统计分析。免疫组织化学分析显示,在检查的208个NPC组织中有132个(63.5%)Aur-A高表达。 Aur-A表达与T分类(P = 0.012),临床分期(P = 0.003)和颅底侵犯(P = 0.003)显着相关。统计分析表明,Aur-A表达与NPC患者10年总体生存率和无病生存率成反比。多元分析的结果表明,Aur-A表达是患者生存的独立预后指标。更重要的是,发现Aur-A是存活不良的标志,这主要归因于Aur-A在T4肿瘤分类亚组中的高表达以及侵袭性局部侵袭。这些结果表明,Aur-A表达与生存成反比,与NPC的恶性程度直接成正比。因此,Aur-A可以作为潜在的生物学标志物,用于预测患者T4亚组的不良预后。

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