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Serum GP73 is complementary to AFP and GGT-II for the diagnosis of hepatocellular carcinoma

机译:血清GP73是AFP和GGT-II的补充可用于诊断肝细胞癌

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摘要

Golgi protein 73 (GP73) is a resident Golgi type II transmembrane protein that has been reported to markedly increase in chronic liver disease, particularly in hepatocellular carcinoma (HCC). However, it remains unclear as to whether serum GP73 represents a reliable serum marker for the diagnosis of HCC. The aim of the present study was to evaluate the diagnostic value of serum GP73 in patients with HCC and to determine the diagnostic accuracy of measuring serum GP73 in combination with α-fetoprotein (AFP) and γ-glutamyl transferase isoenzyme II (GGT-II) in HCC. Serum GP73 was detected using a time-resolved fluorescence immunological assay (TRFIA) and enzyme-linked immunosorbent assay (ELISA) in 79 HCC cases, including 16 liver cirrhosis, 30 chronic hepatitis and 28 healthy individuals. The correlation between serum GP73 and tumor size and HCC grading was analyzed and the complementary diagnostic value of serum GP73, AFP and GGT-II was evaluated. TRFIA was established for the detection of serum GP73 and was sensitive and reproducible. The expression levels of serum GP73 were markedly higher in the patients with HCC when compared with those of the individuals with liver cirrhosis and chronic hepatitis or the healthy individuals. According to the receiver operating characteristic (ROC) curve, diagnostic sensitivity and specificity for HCC with a cut-off value of 78.1 ng/l were 73.4 and 79.0%, respectively. However, no correlation was identified among serum GP73 and tumor size or grading, and no correlations were identified among serum GP73, AFP and GGT-II. The diagnostic sensitivities for HCC, as detected by TRFIA of GP73, AFP and GGT-II, were 73.4, 55.6 and 68.4%, respectively, and the specificities were 80.0, 86.7 and 97.1%, respectively. The combined determination of these markers increased the diagnostic sensitivity to 96.3% for HCC. TRFIA functions as a sensitive and replicable assay for the detection of serum GP73. The levels of serum GP73 were significantly higher in the HCC group when compared with the individuals with benign liver diseases. Serum GP73 may serve as a potential independent diagnostic candidate for HCC and the combined determination of serum GP73, AFP and GGT-II may increase the diagnostic efficiency of HCC.
机译:高尔基体蛋白73(GP73)是驻留的高尔基体II型跨膜蛋白,据报道在慢性肝病,特别是肝细胞癌(HCC)中明显增加。然而,关于血清GP73是否代表诊断HCC的可靠血清标志物尚不清楚。本研究的目的是评估血清GP73在肝癌患者中的诊断价值,并确定结合α-甲胎蛋白(AFP)和γ-谷氨酰转移酶同工酶II(GGT-II)测定血清GP73的诊断准确性。在HCC中。使用时间分辨荧光免疫测定(TRFIA)和酶联免疫吸附测定(ELISA)检测了79例HCC患者的血清GP73,其中包括16例肝硬化,30例慢性肝炎和28例健康个体。分析血清GP73与肿瘤大小和HCC分级之间的相关性,并评估血清GP73,AFP和GGT-II的互补诊断价值。建立了用于检测血清GP73的TRFIA,它灵敏且可重现。与肝硬化和慢性肝炎患者或健康个体相比,HCC患者血清GP73的表达水平显着升高。根据接收器工作特征(ROC)曲线,截断值为78.1 ng / l的HCC的诊断敏感性和特异性分别为73.4%和79.0%。然而,在血清GP73与肿瘤大小或分级之间未发现相关性,并且在血清GP73,AFP和GGT-II之间未发现相关性。 GP73,AFP和GGT-II的TRFIA检测对HCC的诊断敏感性分别为73.4%,55.6%和68.4%,特异性分别为80.0%,86.7%和97.1%。这些标志物的综合测定将对HCC的诊断敏感性提高到96.3%。 TRFIA用作检测血清GP73的灵敏且可复制的测定法。与肝良性疾病患者相比,HCC组的血清GP73水平显着升高。血清GP73可以作为HCC的潜在独立诊断候选物,血清GP73,AFP和GGT-II的联合测定可以提高HCC的诊断效率。

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