Decreased expression of ECRG4 in serum predicts poor prognosis for patients with nasopharyngeal carcinoma

被引:1
作者
Zang, Yanzi [1 ,2 ]
Wan, Baoluo [2 ]
Jia, Xiaodong [2 ]
Lou, Weihua [1 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Zhengzhou 450052, Peoples R China
[2] Peoples Hosp Henan Prov, Zhengzhou 450003, Peoples R China
关键词
ECRG4; nasopharyngeal carcinoma; prognosis; TUMOR-SUPPRESSOR GENE; CANCER-RELATED GENE; ESOPHAGEAL CANCER; ASSOCIATION; TWIST;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The present study tended to explore the expression of esophageal carcinoma related gene 4 (ECRG4) in patients with nasopharyngeal carcinoma (NPC). Besides, the correlation between ECRG4 expression and prognosis of NPC patients was also evaluated. Methods: The relative expression level of ECRG4 mRNA in serum was detected by Quantitative real-time PCR (qRT-PCR). Chi-square test was performed to analyze the relationship between ECRG4 expression and clinical characteristics of NPC patients. Kaplan-Meier method was used to analyze the association of ECRG4 expression and overall survival of NPC patients. Cox regression analysis was conducted to study the role of ECRG4 in the prognosis of NPC patients. Results: ECRG4 was weakly expressed in serum of NPC patients compared to the controls (P < 0.001). There was significant relationship between ECRG4 expression and such clinical characteristics as high TNM stage, metastasis and N classification (P < 0.05). Survival curves illustrated that the survival rate of patients with low ECRG4 was significantly lower than those with high ECRG4 expression (P = 0.003). Cox regression analysis demonstrated that ECRG4 could act as a prognostic factor for NPC patients (P = 0.036, HR = 2.930, 95% CI = 1.072-8.009). Conclusion: ECRG4 expression was tightly related with the prognosis of NPC patients.
引用
收藏
页码:2039 / 2043
页数:5
相关论文
共 27 条
[1]   Molecular screening for Epstein Barr virus (EBV) among Sudanese patients with nasopharyngeal carcinoma (NPC) [J].
Ahmed, Hussain Gadelkarim ;
Suliman, Rania Saad Abdul Gader ;
Abd El Aziz, Mohammed Siddig ;
Alshammari, Fawaz D. .
INFECTIOUS AGENTS AND CANCER, 2015, 10
[2]  
Baird Andrew, 2014, Gastrointest Cancer, V2014, P131
[3]   The tumor-promoting function of ECRG4 in papillary thyroid carcinoma and its related mechanism [J].
Chen, Jiayu ;
Liu, Chibo ;
Yin, Lihui ;
Zhang, Wei .
TUMOR BIOLOGY, 2015, 36 (02) :1081-1089
[4]   ECRG4 is a candidate tumor suppressor gene frequently hypermethylated in colorectal carcinoma and glioma [J].
Goetze, Silke ;
Feldhaus, Valeska ;
Traska, Thilo ;
Wolter, Marietta ;
Reifenberger, Guido ;
Tannapfel, Andrea ;
Kuhnen, Cornelius ;
Martin, Dirk ;
Mueller, Oliver ;
Sievers, Sonja .
BMC CANCER, 2009, 9
[5]   Ecrg4 Attenuates the Inflammatory Proliferative Response of Mucosal Epithelial Cells to Infection [J].
Kurabi, Arwa ;
Pak, Kwang ;
Dang, Xitong ;
Coimbra, Raul ;
Eliceiri, Brian P. ;
Ryan, Allen F. ;
Baird, Andrew .
PLOS ONE, 2013, 8 (04)
[6]   Extracranial carotid artery disease in nasopharyngeal carcinoma patients with post-irradiation ischemic stroke [J].
Li, Chuei-Shiun ;
Schminke, Ulf ;
Tan, Teng-Yeow .
CLINICAL NEUROLOGY AND NEUROSURGERY, 2010, 112 (08) :682-686
[7]   Expression of esophageal cancer related gene 4 (ECRG4), a novel tumor suppressor gene, in esophageal cancer and its inhibitory effect on the tumor growth in vitro and in vivo [J].
Li, Lin-Wei ;
Yu, Xi-Ying ;
Yang, Yang ;
Zhang, Chun-Peng ;
Guo, Li-Ping ;
Lu, Shih-Hsin .
INTERNATIONAL JOURNAL OF CANCER, 2009, 125 (07) :1505-1513
[8]   RETRACTED: The candidate tumor suppressor gene ECRG4 inhibits cancer cells migration and invasion in esophageal carcinoma (Retracted article. See vol. 30, artn no. 19, 2011) [J].
Li, Linwei ;
Zhang, Chunpeng ;
Li, Xiaoyan ;
Lu, ShihHsin ;
Zhou, Yun .
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 2010, 29
[9]   Overexpression of candidate tumor suppressor ECRG4 inhibits glioma proliferation and invasion [J].
Li, Wei ;
Liu, Xinrui ;
Zhang, Bo ;
Qi, Dongxue ;
Zhang, Lihong ;
Jin, Yuhong ;
Yang, Hongfa .
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 2010, 29 :1-7
[10]  
Mori Y, 2007, ONCOL REP, V18, P981