Clinical implication of TMPRSS4 expression in human gallbladder cancer

被引:22
作者
Wu, Xiao-Yang [1 ,2 ]
Zhang, Li [3 ]
Zhang, Ke-Ming [4 ]
Zhang, Ming-Hua [5 ]
Ruan, Ting-Yan [6 ]
Liu, Chao-Ying [6 ]
Xu, Jun-Ying [6 ]
机构
[1] Soochow Univ, Dept Cardiovasc Surg, Affiliated Hosp 1, Suzhou 215006, Jiangsu, Peoples R China
[2] Jiangsu Univ, Dept Gen Surg, Kunshan Peoples Hosp 1, Kunshan 215300, Jiangsu, Peoples R China
[3] Jiangsu Univ, Dept Gastroenterol, Kunshan Peoples Hosp 1, Kunshan 215300, Jiangsu, Peoples R China
[4] Nanjing Med Univ, Dept Minimally Invas Surg, Wuxi Peoples Hosp, Wuxi 214023, Jiangsu, Peoples R China
[5] Jiangsu Univ, Dept Hepatobiliary Surg, Kunshan Peoples Hosp 1, Kunshan 215300, Jiangsu, Peoples R China
[6] Nanjing Med Univ, Dept Med Oncol, Wuxi Peoples Hosp, Wuxi 214023, Jiangsu, Peoples R China
关键词
TMPRSS4; Immunohistochemistry; qRT-PCR; Prognosis; CELL LUNG-CANCER; SERINE PROTEASES; INVASION;
D O I
10.1007/s13277-014-1716-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Altered expression of transmembrane protease/serine 4 (TMPRSS4) is observed in various types of human cancers. However, the clinical significance of TMPRSS4 expression in gallbladder cancer (GBC) remains largely unknown. The present study aims to explore the clinicopathological significance and prognostic value of TMPRSS4 in GBC. The levels of TMPRSS4 mRNA and protein in GBC tissues and adjacent noncancerous tissues were evaluated by quantitative reverse-transcriptase polymerase chain reaction and immunohistochemistry. To investigate the correlations between TMPRSS4 and the clinicopathological features of GBC, the expression of TMPRSS4 in 97 patients with GBC were detected by immunohistochemistry. The correlation of TMPRSS4 expression with patients' survival rate was assessed by Kaplan-Meier and Cox regression. Our results showed that the expression levels of TMPRSS4 mRNA and protein in GBC tissues were both significantly higher than those in adjacent noncancerous tissues. Immunohistochemical staining revealed that high TMPRSS4 expression was closely correlated with tumor size (P = 0.032), histological grade (P = 0.002), pathologic T stage (P = 0.005), clinical stage (P = 0.013), and lymph node metastasis (P = 0.003). Moreover, the results of Kaplan-Meier analysis indicated that a high expression level of TMPRSS4 resulted in a significantly poor prognosis of GBC patients. Multivariate analysis showed that the status of TMPRSS4 expression was an independent prognostic factor for GBC patients. Our results showed that TMPRSS4 plays a key role in GBC and therefore may provide an opportunity for developing a novel therapeutic target as well as a prognostic marker in GBC.
引用
收藏
页码:5481 / 5486
页数:6
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