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Dickkopf-1 与可溶性 Axl 联合应用提高丙型肝炎患者肝癌诊断效能。

The Combined Use of Dickkopf-1 and Soluble Axl Improves Hepatocellular Carcinoma Diagnostic Efficacy in Hepatitis C Patients.

机构信息

Department of Chemistry, Faculty of Science, Mansoura University, Egypt.

Gastroenterology Surgical Center, Mansoura University, Egypt.

出版信息

Asian Pac J Cancer Prev. 2024 Jun 1;25(6):2185-2191. doi: 10.31557/APJCP.2024.25.6.2185.

DOI:10.31557/APJCP.2024.25.6.2185
PMID:38918682
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11382852/
Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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。

方法

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。

结果

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。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd3e/11382852/f782c8416b6a/APJCP-25-2185-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd3e/11382852/5637f7356811/APJCP-25-2185-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd3e/11382852/4746301249e2/APJCP-25-2185-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd3e/11382852/f782c8416b6a/APJCP-25-2185-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd3e/11382852/5637f7356811/APJCP-25-2185-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd3e/11382852/4746301249e2/APJCP-25-2185-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd3e/11382852/f782c8416b6a/APJCP-25-2185-g003.jpg

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Gas6 in chronic liver disease-a novel blood-based biomarker for liver fibrosis.慢性肝病中的Gas6——一种新型的基于血液的肝纤维化生物标志物。
Cell Death Discov. 2023 Aug 2;9(1):282. doi: 10.1038/s41420-023-01551-6.
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Recent advances in recurrent hepatocellular carcinoma therapy.复发性肝细胞癌治疗的最新进展
World J Hepatol. 2023 Apr 27;15(4):460-476. doi: 10.4254/wjh.v15.i4.460.
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Current Status of Management of Hepatocellular Carcinoma in The Gulf Region: Challenges and Recommendations.海湾地区肝细胞癌的管理现状:挑战与建议
Cancers (Basel). 2023 Mar 28;15(7):2001. doi: 10.3390/cancers15072001.
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DKK1-CKAP4 signal axis promotes hepatocellular carcinoma aggressiveness.DKK1-CKAP4 信号轴促进肝癌侵袭性。
Cancer Sci. 2023 May;114(5):2063-2077. doi: 10.1111/cas.15743. Epub 2023 Mar 9.
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Circulating tumor cells as a prognostic biomarker in patients with hepatocellular carcinoma.循环肿瘤细胞作为肝细胞癌患者的预后生物标志物。
Sci Rep. 2022 Nov 4;12(1):18686. doi: 10.1038/s41598-022-21888-9.
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Global burden of primary liver cancer in 2020 and predictions to 2040.2020 年全球原发性肝癌负担及 2040 年预测。
J Hepatol. 2022 Dec;77(6):1598-1606. doi: 10.1016/j.jhep.2022.08.021. Epub 2022 Oct 5.
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Blood-based biomarkers for hepatocellular carcinoma screening: Approaching the end of the ultrasound era?基于血液的肝细胞癌筛查生物标志物:即将结束超声时代?
J Hepatol. 2023 Jan;78(1):207-216. doi: 10.1016/j.jhep.2022.08.036. Epub 2022 Sep 8.
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