Prognosis value of mitotic kinase Aurora-A for primary duodenal adenocarcinoma
Prognosis value of mitotic kinase Aurora-A for primary duodenal adenocarcinoma
复制标题
有丝分裂激酶Aurora-A对原发性十二指肠腺癌的预后价值
DOI：
10.1007/s13277-014-2215-3
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发表时间：
2014-09-01
期刊：
影响因子：
--
通讯作者：
Wu, Xiang-Yuan
中科院分区：
文献类型：
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作者：
Chen, Jie;Lin, Qu;Wu, Xiang-Yuan
Others and we have demonstrated that hypoxia-inducible factor 1 alpha (HIF-1 alpha) and transcriptionally upregulated Aurora-A are required for disease progression in several tumors. We investigated the clinicopathological value of HIF-1 alpha and Aurora-A in primary duodenal adenocarcinoma (PDA). Using immunohistochemistry, we evaluated Aurora-A and HIF-1 alpha expression semiquantitatively in 140 PDA cases. There were 76 cases from one institute that formed the training set; 64 cases from another two institutes were used as the testing set to validate the prognostic value of Aurora-A and HIF-1 alpha expression. Aurora-A expression was high or sufficient in the tumor zone, whereas expression was low in the adjacent normal epithelia. High Aurora-A expression, identified using the training set receiver operator characteristic (ROC) analysis-generated cutoff score, predicted poorer overall survival both in the testing set (18.0 vs. 45.1 %, P = 0.001) and training set (23.1 vs. 53.9 %, P = 0.011). Multivariate Cox regression confirmed that Aurora-A was an independent prognostic factor. Contrary to previous studies, we did not detect any correlation between Aurora-A and HIF-1 alpha. Survival analysis showed that HIF-1 alpha level was not correlated with patient outcome (P = 0.466). Activation of Aurora-A, an independent negative prognostic biomarker, might be used to identify particular PDA patients for more selective therapy.
