| Literature DB >> 29113278 |
Min Dong1, Zhan-Hong Chen1,2, Xing Li1, Xiao-Yun Li1,3, Jing-Yun Wen1, Qu Lin1, Xiao-Kun Ma1, Li Wei1, Jie Chen1, Dan-Yun Ruan1, Ze-Xiao Lin1, Tian-Tian Wang1, Dong-Hao Wu1, Xiang-Yuan Wu1.
Abstract
Serum Golgi protein 73 (sGP73) is a candidate diagnostic biomarker for hepatocellular carcinoma (HCC). However, current evidence of its diagnostic value is conflicting, primarily due to the small sample sizes of previous studies, and its prognostic role in HCC also remains unclear. In the present study, sGP73 levels in 462 patients with HCC, 186 patients with liver cirrhosis, and 83 healthy controls were evaluated using ELISA, and it was identified that the median sGP73 levels were significantly higher in the HCC (18.7 ng/ml) and liver cirrhosis (18.5 ng/ml) patients than in the healthy controls (0 ng/ml; both P<0.001); however, the levels did not significantly differ between the HCC and liver cirrhosis groups (P=0.632). sGP73 had an inferior sensitivity and specificity for HCC diagnosis (27.79 and 77.96%, respectively) compared with α-fetoprotein (57.36 and 90.96%, respectively; P<0.001). In the HCC group, a high level of sGP73 was associated with aggressive clinicopathological features and independently predicted poor overall survival (OS) time (P<0.001). Additionally, in patients with resectable HCC, a high level of sGP73 was associated with significantly decreased disease-free survival (P<0.001) and OS (P=0.039) times compared with a low level of sGP73. This study demonstrated that sGP73 is unsuitable as a diagnostic marker for the early detection of HCC; however, it is an independent negative prognostic marker, providing a novel risk stratification factor and a potential therapeutic molecular target for HCC.Entities:
Keywords: Golgi protein 73; hepatocellular carcinoma; prognosis; serum
Year: 2017 PMID: 29113278 PMCID: PMC5661440 DOI: 10.3892/ol.2017.6938
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967