Back to Search Start Over

Decreased CRHBP expression is predictive of poor prognosis in patients with hepatocellular carcinoma.

Authors :
Xia, Hai-Bing
Wang, Hui-Ju
Fu, Luo-Qin
Wang, Shi-Bing
Li, Li
Ru, Guo-Qing
He, Xiang-Lei
Tong, Xiang-Min
Mou, Xiao-Zhou
Huang, Dong-ShENg
Source :
Oncology Letters; Sep2018, Vol. 16 Issue 3, p3681-3689, 9p, 1 Diagram, 3 Charts, 5 Graphs
Publication Year :
2018

Abstract

Corticotropin releasing hormone binding protein (CRHBP) mediates the reaction between corticotropin releasing hormone (CRH) and corticotropin releasing hormone receptors (CRHRs). It is expressed in a number of organs, and the expression of CRHBP is associated with tumorigenesis and cancer progression. The aim of the present study was to investigate CRHBP expression levels in hepatocellular carcinoma (HCC) and its association with patient clinicopathological characteristics as well as prognosis. The expression of CRHBP was examined by immunohistochemistry in 169 HCC tissues and 151 adjacent non‑tumorous tissues. The results were validated by western blotting using patient tissues and liver cancer cell lines. The association of CRHBP expression with clinicopathological patient characteristics and survival rate was analyzed statistically. Expression of CRHBP was detected in 142/151 (94.0%) non‑tumorous liver tissues, and 84/169 (49.7%) HCC tissues (P<0.001). The expression of CRHBP was negatively associated with tumor size (P=0.013), Edmondson Grade (P=0.002), hepatitis B virus antigen (P=0.020), and α‑fetoprotein levels (P=0.014). Patients exhibiting low CRHBP expression were associated with shorter survival time compared with those exhibiting high CRHBP expression (P=0.012). The results of western blotting analysis suggest that reduced CRHBP expression is frequently observable in patients with HCC. Low CRHBP expression in HCC tissues may be a predictor of clinical prognosis and a potential therapeutic target for HCC. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17921074
Volume :
16
Issue :
3
Database :
Complementary Index
Journal :
Oncology Letters
Publication Type :
Academic Journal
Accession number :
131270854
Full Text :
https://doi.org/10.3892/ol.2018.9073