Kim Ji-Myung, Yeo Min-Kyung, Lim Jae Sung, Song In-Sang, Chun Kwangsik, Kim Kyung-Hee
Department of Laboratory Medicine, Chungnam National University Hospital, 282 Munwha-ro, Daejeon 35015, Korea.
Department of Pathology, Chungnam National University School of Medicine, 266 Munhwa Street, Daejeon 35015, Korea.
J Clin Med. 2019 Aug 1;8(8):1151. doi: 10.3390/jcm8081151.
Apurinic/apyrimidinic endonuclease 1/redox effector factor 1 (APEX1) has been known to play key roles in DNA repair, the regulation of diverse transcriptional activity, and cellular responses to redox activity. This study aimed to examine serum APEX1 (s-APEX1) expression as a possible screening biomarker for clear cell renal cell carcinoma (ccRCC), hepatocellular carcinoma (HCC), and proximal and distal cholangiocarcinoma (CC). A total of 216 frozen serum samples were collected from 39 healthy control cases, 32 patients with ≥58 copies/mL of hepatitis B viral DNA (HBV DNA (+)), 40 ccRCC cases, 59 HCC cases, and 46 CC cases. The serum samples were examined for s-APEX1 concentration by enzyme-linked immunosorbent assay. The association of APEX1 expression with clinicopathological characteristics was also studied by immunohistochemical staining in 106 ccRCC, 131 HCC, and 32 intrahepatic CC cases. The median s-APEX1 concentrations of the HCC, CC, ccRCC, healthy control, and HBV DNA (+) groups were 0.294, 0.710, 0.474, 0.038, and 2.384 ng/mL, respectively ( < 0.001). Univariate and multivariate analyses revealed that increased cytoplasmic APEX1 expression led to a shorter disease-free survival period in HCC and CC cases. We suggest that the s-APEX1 level could be a potential diagnostic biomarker of ccRCC, HCC, and CC. Additionally, cytoplasmic APEX1 expression in cancer cells could be used to predict relapses in patients with HCC or CC.
无嘌呤/无嘧啶内切酶1/氧化还原效应因子1(APEX1)在DNA修复、多种转录活性的调节以及细胞对氧化还原活性的反应中发挥关键作用。本研究旨在检测血清APEX1(s-APEX1)表达,将其作为肾透明细胞癌(ccRCC)、肝细胞癌(HCC)以及肝内、外胆管癌(CC)的一种可能的筛查生物标志物。共收集了216份冷冻血清样本,来自39例健康对照者、32例乙肝病毒DNA(HBV DNA)≥58拷贝/mL的患者(HBV DNA(+))、40例ccRCC患者、59例HCC患者以及46例CC患者。采用酶联免疫吸附测定法检测血清样本中的s-APEX1浓度。还通过免疫组织化学染色对106例ccRCC、131例HCC和32例肝内CC病例研究了APEX1表达与临床病理特征的相关性。HCC、CC、ccRCC、健康对照和HBV DNA(+)组的s-APEX1浓度中位数分别为0.294、0.710、0.474、0.038和2.384 ng/mL(<0.001)。单因素和多因素分析显示,HCC和CC病例中,细胞质APEX1表达增加导致无病生存期缩短。我们认为,s-APEX1水平可能是ccRCC、HCC和CC的潜在诊断生物标志物。此外,癌细胞中的细胞质APEX1表达可用于预测HCC或CC患者的复发情况。