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Serum Golgi protein 73 is a prognostic rather than diagnostic marker in hepatocellular carcinoma

机译:血清高尔基蛋白73是肝细胞癌的预后而非诊断标志物

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摘要

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.
机译:血清高尔基蛋白73(sGP73)是肝细胞癌(HCC)的候选诊断生物标志物。但是,目前有关其诊断价值的证据相互矛盾,这主要是由于先前研究的样本量较小,并且其在HCC中的预后作用也不清楚。在本研究中,使用ELISA对462例HCC患者,186例肝硬化患者和83例健康对照者的sGP73水平进行了评估,结果发现,在肝癌中,sGP73的中位数显着更高(18.7 ng / ml)。肝硬化(18.5 ng / ml)患者比健康对照组(0 ng / ml;均P <0.001);但是,肝癌和肝硬化组之间的水平没有显着差异(P = 0.632)。 sGP73对HCC诊断的敏感性和特异性较低(分别为27.79和77.96%),而α-甲胎蛋白(分别为57.36和90.96%; P <0.001)。在HCC组中,高水平的sGP73与侵略性临床病理特征相关,并独立预测总体生存(OS)时间较差(P <0.001)。另外,在可切除的肝癌患者中,与低水平的sGP73相比,高水平的sGP73与无病生存期(P <0.001)和OS(P = 0.039)时间显着降低有关。这项研究表明,sGP73不适合作为早期检测HCC的诊断标记。然而,它是一个独立的阴性预后指标,为HCC提供了新的风险分层因子和潜在的治疗分子靶标。

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