Department of Gastroenterology and Hepatology, Japan Community Health Care Organization Shimonoseki Medical Center, Shimonoseki, Yamaguchi 7500061, Japan.
Department of Physiology, Faculty of Medicine, Saitama Medical University, Iruma-gun, Saitama 3500495, Japan.
World J Gastroenterol. 2020 Apr 7;26(13):1463-1473. doi: 10.3748/wjg.v26.i13.1463.
The prognosis of hepatocellular carcinoma (HCC) patients remains poor despite advances in treatment modalities and diagnosis. It is important to identify useful markers for the early detection of HCC in patients. Preneoplastic antigen (PNA), originally reported in a rat carcinogenesis model, is increased in the tissues and serum of HCC patients.
To determine the diagnostic value of PNA for discriminating HCC and to characterize PNA-positive HCC.
Patients with hepatitis C virus (HCV)-related hepatic disorders were prospectively enrolled in this study, which included patients with hepatitis, with cirrhosis, and with HCC. A novel enzyme-linked immunosorbent assay was developed to measure serum PNA concentrations in patients.
Serum PNA concentrations were measured in 89 controls and 141 patients with HCV infections (50 hepatitis, 44 cirrhosis, and 47 HCC). Compared with control and non-HCC patients, PNA was increased in HCC. On receiver operating characteristic curve analysis, the sensitivity of PNA was similar to the HCC markers des-γ-carboxy-prothrombin (DCP) and α-fetoprotein (AFP), but the specificity of PNA was lower. There was no correlation between PNA and AFP and a significant but weak correlation between PNA and DCP in HCC patients. Importantly, the correlations with biochemical markers were completely different for PNA, AFP, and DCP; glutamyl transpeptidase was highly correlated with PNA, but not with AFP or DCP, and was significantly higher in PNA-high patients than in PNA-low patients with HCV-related HCC.
PNA may have the potential to diagnose a novel type of HCC in which glutamyl transpeptidase is positively expressed but AFP or DCP is weakly or negatively expressed.
尽管治疗方式和诊断技术有所进步,肝细胞癌(HCC)患者的预后仍然较差。因此,确定 HCC 患者早期检测的有用标志物非常重要。癌前期抗原(PNA)最初在大鼠致癌模型中报道,在 HCC 患者的组织和血清中增加。
确定 PNA 区分 HCC 的诊断价值,并对 PNA 阳性 HCC 进行特征描述。
本研究前瞻性纳入了丙型肝炎病毒(HCV)相关肝脏疾病患者,包括肝炎、肝硬化和 HCC 患者。开发了一种新的酶联免疫吸附试验来测量患者血清 PNA 浓度。
在 89 名对照和 141 名 HCV 感染患者(50 名肝炎、44 名肝硬化和 47 名 HCC)中测量了血清 PNA 浓度。与对照和非 HCC 患者相比,PNA 在 HCC 中增加。在接收者操作特征曲线分析中,PNA 的灵敏度与 HCC 标志物脱-γ-羧基凝血酶原(DCP)和甲胎蛋白(AFP)相似,但 PNA 的特异性较低。在 HCC 患者中,PNA 与 AFP 之间没有相关性,与 DCP 之间存在显著但较弱的相关性。重要的是,PNA、AFP 和 DCP 与生化标志物的相关性完全不同;谷氨酰转肽酶与 PNA 高度相关,但与 AFP 或 DCP 不相关,并且在 HCV 相关 HCC 的 PNA 高患者中明显高于 PNA 低患者。
PNA 可能具有诊断新型 HCC 的潜力,在这种 HCC 中,谷氨酰转肽酶呈阳性表达,但 AFP 或 DCP 呈弱阳性或阴性表达。