Open AccessExpression and significance of caveolin‑1 in hepatitis B virus‑associated hepatocellular carcinoma
Author(s) -
Hao Cheng,
Yunlong Pan,
Yongzhong Yao,
Zhenxi Zhu,
Jun Chen,
Xueying Sun,
Yudong Qiu,
Yitao Ding
Publication year - 2017
Publication title -
experimental and therapeutic medicine
Language(s) - English
Resource type - Journals
eISSN - 1792-1015
pISSN - 1792-0981
DOI - 10.3892/etm.2017.5038
Subject(s) - hepatocellular carcinoma , cirrhosis , hepatitis b virus , angiogenesis , immunohistochemistry , medicine , pathology , oncogene , vascular endothelial growth factor , hepatitis b , liver cancer , cancer research , cancer , virus , immunology , cell cycle , vegf receptors
Caveolin-1 (Cav-1) is a major component of caveolae and has been recently identified as a tumor suppressor. As little is known about Cav-1 in hepatitis B virus (HBV)-associated hepatocellular carcinoma (HCC), the aim of the present study was to investigate the expression and significance of Cav-1 in HBV-associated HCC. Semi-quantitative reverse transcription-polymerase chain reaction (RT-PCR) was performed to detect the mRNA expression level of Cav-1 in 40 cases of HBV-associated HCC, the corresponding 11 non-tumor cases of HBV-associated chronic hepatitis, 29 non-tumor cases of HBV-associated cirrhosis and 6 cases of normal liver tissues. Immunohistochemical analysis indicated the expression of Cav-1, cluster of differentiation 34 and vascular endothelial growth factor (VEGF) in HBV-associated HCC tissue samples. In addition, the association of Cav-1 expression with angiogenesis and clinicopathological characteristics of HBV-associated HCC was also analyzed. RT-PCR results demonstrated that the expression rate of Cav-1 mRNA in HBV-associated HCC, non-tumor HBV-associated chronic hepatitis and cirrhosis liver tissues and control normal liver tissues from patients with metastatic carcinoma was 92.5, 85.0 and 16.7%, respectively. mRNA expression level of Cav-1 was significantly increased in chronic hepatitis, cirrhosis and HBV-associated HCC livers compared with normal control livers (P<0.05 and P<0.01, respectively). Cav-1 protein was detected by immunohistochemistry in 80% of the samples of HBV-associated HCC. Furthermore, Cav-1 and VEGF protein expression levels were correlated with microvessel density (MVD; γ s <0.46, P=0.01 and γ s <0.31, P=0.05, respectively). In addition, Cav-1 expression and MVD were significantly associated with metastasis (P=0.031 and P=0.046, respectively). In conclusion, Cav-1 may have an important role in the carcinogenesis and progression of HBV-associated HCC and angiogenesis may be affected by Cav-1 during this process.