High levels of EphA3 expression are associated with high invasive capacity and poor overall survival in hepatocellular carcinoma

被引:25
|
作者
Lu, Cheng-Yi [1 ]
Yang, Zhao-Xu [2 ]
Zhou, Liang [3 ]
Huang, Zhi-Zhong [1 ]
Zhang, Hong-Tao [2 ]
Li, Jun [2 ]
Tao, Kai-Shan [2 ]
Xie, Bai-Zhi [4 ]
机构
[1] Fourth Mil Med Univ, Tangdu Hosp, Dept Informat, Xian 710032, Shannxi, Peoples R China
[2] Fourth Mil Med Univ, Xijing Hosp, Dept Hepatobiliary Surg, Xian 710032, Shannxi, Peoples R China
[3] 155 Cent Hosp PLA, Dept Gen Surg, Kaifeng 471000, Henan, Peoples R China
[4] Fourth Mil Med Univ, Xian 710032, Shannxi, Peoples R China
关键词
hepatocellular carcinoma; EphA3; invasion; overall survival; clinicopathological correlation; ENDOTHELIAL GROWTH-FACTOR; RECEPTOR TYROSINE KINASES; EPHRIN LIGANDS; GENE; TUMOR; PROTEIN; HEK; PROLIFERATION; ANGIOGENESIS; METASTASIS;
D O I
10.3892/or.2013.2679
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although EphA3 expression has been associated with progression or prognosis in several types of tumors, the role of EphA3 in hepatocellular carcinoma (HCC) remains unknown. This study sought to investigate the clinicopathological and prognostic relevance of EphA3 expression in HCC as well as the underlying mechanisms responsible. EphA3 protein was mainly localized within the cytoplasm and at the cell membrane. High EphA3 expression was correlated with tumor size, tumor grade, metastasis, venous invasion and AJCC TNM stage (P<0.05), and patients with high levels of EphA3 expression were at a significantly increased risk for shortened survival time (P<0.05). In vitro, the downregulation of EphA3 expression decreased the invasive capacity of HCC cells via the regulation of VEGF. EphA3 may represent a novel candidate marker for patient prognosis as well a molecular target for HCC therapy.
引用
收藏
页码:2179 / 2186
页数:8
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