Department of Chemistry, Faculty of Science, Mansoura University, Egypt.
Gastroenterology Surgical Center, Mansoura University, Egypt.
Asian Pac J Cancer Prev. 2024 Jun 1;25(6):2185-2191. doi: 10.31557/APJCP.2024.25.6.2185.
Standard tools are not sensitive enough for hepatocellular carcinoma (HCC) early detection. This study aimed to evaluate the accuracy of dickkopf-1 (DKK1) and soluble Axl (sAxl) and their combined for early differentiating of HCC from premalignant benign liver diseases.
A total of 210 chronic hepatitis C (CHC) patients (55 fibrotic, 45 cirrhotic and 110 HCC) were enrolled. Both DKK1 and sAxl were tested using ELISA for all participants.
HCC patients were accompanied by a significant increase (P<0.05) in DKK1 (5.38±2.05 ng/mL) and sAxl (178.02±49.39 ng/mL) compared to patients with fibrosis (2.16±0.6, 97.63±19.71 ng/mL, respectively) and cirrhosis (2.62±0.8, 121.84±34.66 ng/mL, respectively). Both DKK1 (AUC=0.852) and sAxl (AUC=0.882) had a good diagnostic accuracy in separating HCC from all non-HCC patients. Multiplying DKK1 with sAXL yielded values that significantly (P=0.0001) increased in patients who developed HCC (674.3 (434.2-1413.9)) versus fibrotic (204.9 (161.7-262)) and cirrhotic (254.4 (205.4-343.7)) patients. This model improves HCC diagnostic performances [AUC=0.921; sensitivity 90.9%, specificity 87%, PPV 88.5%, NPV 89.7% and efficiency 89.1%]. Elevated DKK1×sAxl values were associated with aggressive tumor features including multiple nodules, large size, Child-Pugh and BCLC late stages.
combined use of DKK1×sAxl is simple and feasible HCC diagnostic model that could enhance HCC diagnostic accuracy and could replace AFP in follow up of patients with premalignant diseases.
标准工具对于肝细胞癌 (HCC) 的早期检测不够敏感。本研究旨在评估 Dickkopf-1 (DKK1) 和可溶性 Axl (sAxl) 的准确性,以及它们联合用于早期区分 HCC 与癌前良性肝病。
共纳入 210 名慢性丙型肝炎 (CHC) 患者(55 名纤维化,45 名肝硬化,110 名 HCC)。所有参与者均使用 ELISA 检测 DKK1 和 sAxl。
与纤维化患者(2.16±0.6ng/mL,97.63±19.71ng/mL)和肝硬化患者(2.62±0.8ng/mL,121.84±34.66ng/mL)相比,HCC 患者的 DKK1(5.38±2.05ng/mL)和 sAxl(178.02±49.39ng/mL)显著升高(P<0.05)。DKK1(AUC=0.852)和 sAxl(AUC=0.882)在区分 HCC 与所有非 HCC 患者方面均具有良好的诊断准确性。将 DKK1 与 sAXL 相乘,结果显示在发生 HCC 的患者中(674.3(434.2-1413.9))显著高于纤维化患者(204.9(161.7-262))和肝硬化患者(254.4(205.4-343.7))(P=0.0001)。该模型提高了 HCC 的诊断性能[AUC=0.921;灵敏度 90.9%,特异性 87%,PPV 88.5%,NPV 89.7%和效率 89.1%]。升高的 DKK1×sAxl 值与多个结节、大肿瘤、Child-Pugh 和 BCLC 晚期等侵袭性肿瘤特征相关。
DKK1×sAxl 的联合使用是一种简单可行的 HCC 诊断模型,可提高 HCC 的诊断准确性,并可替代 AFP 用于癌前疾病患者的随访。