Evidence map›Paper›PMID 38918682›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2024

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

Ereny Samuell, Abdel-Aziz F Abdel-Aziz, Ahmed S Shehata, Mohamed Abdel-Wahab, Rehab A Elmougy

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Article in Asian Pacific journal of cancer prevention : APJCP, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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5 authors.

Ereny SamuellDepartment of Chemistry, Faculty of Science, Mansoura University, Egypt.
Abdel-Aziz F Abdel-AzizDepartment of Chemistry, Faculty of Science, Mansoura University, Egypt.
Ahmed S ShehataGastroenterology Surgical Center, Mansoura University, Egypt.
Mohamed Abdel-WahabGastroenterology Surgical Center, Mansoura University, Egypt.
Rehab A ElmougyDepartment of Chemistry, Faculty of Science, Mansoura University, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStandard 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.

methodsA 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.

resultsHCC 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.

conclusionscombined 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.

Indexed as

Axl Receptor Tyrosine KinaseBiomarkers, TumorCarcinoma, HepatocellularHepatitis C, ChronicIntercellular Signaling Peptides and ProteinsLiver NeoplasmsProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesAdultAgedEarly Detection of CancerFemaleFollow-Up StudiesHepacivirusHumansLiver CirrhosisAXL protein, humanAxl Receptor Tyrosine KinaseBiomarkers, TumorDKK1 protein, humanIntercellular Signaling Peptides and ProteinsProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesDKK1early detectionHCCHCVsoluble Axl

Identifiers

PMID38918682
PMCPMC11382852

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.