Department of Molecular Diagnosis, Graduate School of Medicine, Chiba University and Divisions of Laboratory Medicine, Clinical Genetics and Proteomics, Chiba University Hospital, Chiba, Japan.
Biochem Biophys Res Commun. 2012 May 18;421(4):837-43. doi: 10.1016/j.bbrc.2012.04.099. Epub 2012 Apr 25.
Hepatocellular carcinoma (HCC), the predominant form of primary liver cancer, is one of the most common cancers worldwide and the third most common cause of cancer-related death. Imaging studies including ultrasound and computed tomography are recommended for early detection of HCC, but they are operator dependent, costly and involve radiation. Therefore, there is a need for simple and sensitive serum markers for the early detection of hepatocellular carcinoma (HCC). In our recent proteomic studies, a number of proteins overexpressed in HCC tissues were identified. We thought if the serum autoantibodies to these overexpressed proteins were detectable in HCC patients. Of these proteins, we focused on Ku86, a nuclear protein involved in multiple biological processes and aimed to assess the diagnostic value of serum anti-Ku86 in the early detection of HCC. Serum samples were obtained prior to treatment from 58 consecutive patients with early or relatively early hepatitis C virus (HCV)-related HCC and 137 patients with HCV-related liver cirrhosis without evidence of HCC. Enzyme immunoassays were used to measure serum levels of autoantibodies. Serum levels of anti-Ku86 antibodies were significantly elevated in HCC patients compared to those in liver cirrhosis patients (0.41±0.28 vs. 0.18±0.08Abs at 450nm, P<0001). Setting the cut-off level to give 90% specificity, anti-Ku86 was positive in 60.7% of stage I solitary tumor <2cm in diameter, whereas the sensitivities of alpha-fetoprotein (AFP) and protein induced by vitamin K absence or antagonist II (PIVKA-II) were 17.8% and 21.4%, respectively. The results of ROC analyses indicated the better performance of anti-Ku86 for early detection of HCC. Serum anti-Ku86 levels decreased after surgical resection of the tumors in the 12 HCC cases tested, Elevation of anti-Ku86 in solid tumors other than liver was minimal. Serum anti-Ku86 is a potential biomarker for early detection of HCV-related HCC. Further studies in a larger number of HCC patients with various etiologies are needed to further evaluate the diagnostic and pathophysiological roles of elevation of serum anti-Ku86 in early HCC.
肝细胞癌(HCC)是原发性肝癌的主要形式,是全球最常见的癌症之一,也是癌症相关死亡的第三大主要原因。包括超声和计算机断层扫描在内的影像学研究被推荐用于早期发现 HCC,但它们依赖于操作者、成本高昂且涉及辐射。因此,需要一种简单而敏感的血清标志物来早期检测肝细胞癌(HCC)。在我们最近的蛋白质组学研究中,鉴定出了在 HCC 组织中过度表达的许多蛋白质。我们认为,如果这些过度表达的蛋白质在 HCC 患者的血清中可检测到自身抗体。在这些蛋白质中,我们专注于 Ku86,一种参与多种生物学过程的核蛋白,并旨在评估血清抗 Ku86 在早期检测 HCC 中的诊断价值。在治疗前,从 58 例连续的早期或相对早期丙型肝炎病毒(HCV)相关 HCC 患者和 137 例无 HCC 证据的 HCV 相关肝硬化患者中获得血清样本。酶免疫测定用于测量血清自身抗体水平。与肝硬化患者相比,HCC 患者的血清抗 Ku86 抗体水平显着升高(450nm 处为 0.41±0.28 与 0.18±0.08Abs,P<0001)。将截止值设置为 90%特异性,60.7%直径<2cm 的 I 期单发肿瘤的抗 Ku86 呈阳性,而甲胎蛋白(AFP)和维生素 K 缺乏或拮抗剂 II 诱导蛋白(PIVKA-II)的灵敏度分别为 17.8%和 21.4%。ROC 分析结果表明,抗 Ku86 对早期检测 HCC 的性能更好。在 12 例经测试的 HCC 病例中,肿瘤切除后血清抗 Ku86 水平下降,除肝脏以外的实体瘤中抗 Ku86 升高最小。血清抗 Ku86 是早期检测 HCV 相关 HCC 的潜在生物标志物。需要对更多具有不同病因的 HCC 患者进行更大规模的研究,以进一步评估血清抗 Ku86 升高在早期 HCC 中的诊断和病理生理作用。