Expression of EIF5A2 associates with poor survival of nasopharyngeal carcinoma patients treated with induction chemotherapy

BMC Cancer

Research Article

Ting-Ting Zeng¹  Xiaojiao Ban¹  Bao-Zhu Zhang¹  Wen-Feng Hua¹  Meng-Qing Li¹  Ying-Hui Zhu¹  Xin-Yuan Guan²  Li Zhang³  Hai-Qiang Mai⁴  Pei-Yu Huang⁴  Yan Li⁵ 

[1] State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Collaborative Innovation Center of Cancer Medicine, Guangzhou, China;State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Collaborative Innovation Center of Cancer Medicine, Guangzhou, China;Department of Clinical Oncology, The University of Hong Kong, Hong Kong, China;Room 706, Building 2, No.651 East Dongfeng Road, 510060, Guangzhou, Guangdong, China;State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Collaborative Innovation Center of Cancer Medicine, Guangzhou, China;Department of Medical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, China;State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Collaborative Innovation Center of Cancer Medicine, Guangzhou, China;Department of Nasopharyngeal Carcinoma, Sun Yat-sen University Cancer Center, Guangzhou, China;State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Collaborative Innovation Center of Cancer Medicine, Guangzhou, China;Room 706, Building 2, No.651 East Dongfeng Road, 510060, Guangzhou, Guangdong, China;

关键词: Nasopharyngeal carcinoma;    Gene amplification;    EIF5A2;    Prognosis;   

DOI  :  10.1186/s12885-016-2714-2

 received in 2015-04-29, accepted in 2016-08-03,  发布年份 2016

来源: Springer

【 摘 要 】

BackgroundNasopharyngeal carcinoma (NPC) is a type of head-neck cancer with a distinguishable geographic and racial distribution worldwide. Increasing evidence supports that the accumulation of additional genetic and epigenetic abnormalities is important in driving the NPC tumorigenic process. In this study, we aim to investigate the association between EIF5A2 (Eukaryotic translation initiation factor 5A2) expression status and NPC clinical outcomes.MethodsThe expression status of EIF5A2 was investigated in the NPC tissue microarray. Tissues were from 166 NPC patients staging II-IV, collected between 1999 and 2005. All patients were administered 2–3 cycles of DDP (cisplatin) + 5-Fu (5-fluorouracil) induction therapy and then treated with a uniform conventional two-dimensional radiotherapy. Cell motility assay, tumor growth assay and cytotoxicity assay were performed on the EIF5A2 overexpressed cells and control cells. siRNA was also used in the in vitro studies.ResultsPositive staining of EIF5A2 was observed in 85.4 % (105/123) informative tumor cases. Multivariate analyses demonstrated that EIF5A2 was an independent prognostic marker of poor overall survival (OS) (P = 0.041), failure-free survival (FFS) (P = 0.029), and distant failure-free survival (D-FFS) (P = 0.043) in patients with locoregionally advanced NPC patients treated with cisplatin + 5-Fu chemoradiotherapy. The forced expression of EIF5A2 in NPC cells enhanced the cells’ motility and growth ability. Knock-down of EIF5A2 in NPC cells decreased the cell’s motility and growth ability. Our results also demonstrated that EIF5A2 overexpression induced chemoresistance of NPC cells to 5-Fu.ConclusionsOur findings suggested that EIF5A2 expression, as examined by immunohistochemistry, could function as an independent prognostic factor of outcomes in NPC patients with cisplatin + 5-Fu chemoradiotherapy. EIF5A2 might be a novel therapeutic target for the inhibition of NPC progress.

【 授权许可】

CC BY   
© Huang et al. 2016