Systematic review: Glycomics as diagnostic markers for hepatocellular carcinoma

Author:

Butaye Emma12ORCID,Somers Nicky12,Grossar Lorenz12,Pauwels Nele3,Lefere Sander12ORCID,Devisscher Lindsey24,Raevens Sarah25,Geerts Anja25,Meuris Leander67,Callewaert Nico67,Van Vlierberghe Hans25,Verhelst Xavier25ORCID

Affiliation:

1. Hepatology Research Unit, Department of Internal Medicine and Pediatrics Ghent University Ghent Belgium

2. Liver Research Center Ghent Ghent University, Ghent University Hospital Ghent Belgium

3. Knowledge Center for Health Ghent Ghent University Hospital, Ghent University Ghent Belgium

4. Gut‐Liver Immunopharmacology Unit, Department of Basic and Applied Medical Sciences Ghent University Ghent Belgium

5. Department of Gastroenterology and Hepatology Ghent University Hospital Ghent Belgium

6. Department of Biochemistry and Microbiology VIB‐UGent Center for Medical Biotechnology Ghent Belgium

7. Department of Biochemistry and Microbiology Ghent University Ghent Belgium

Abstract

SummaryBackgroundHepatocellular carcinoma (HCC) is the most prevalent primary liver cancer with one of the highest cancer‐related mortality rates worldwide. Early diagnosis is crucial for improving the therapeutic options and reducing the disease‐related mortality.AimTo investigate serum N‐glycomics as diagnostic markers for HCC.MethodsWe performed a comprehensive search in PubMed, EMBASE, Web of Science and Scopus through August 17, 2023. Eligible studies assessed the potential use of serum N‐glycomics as diagnostic biomarkers for HCC. Study selection, data extraction and quality assessment were performed by two independent reviewers.ResultsOf the 48 articles included, 11 evaluated the utility of N‐glycomics for the diagnosis of HCC in whole serum while the remaining articles focused on specific protein glycoforms or protein levels. Of these specific proteins, haptoglobin, alpha‐fetoprotein (AFP), kininogen (Kin), α‐1‐antitrypsin and Golgi protein 73 (GP73) were the most frequently studied. Increased levels of fucosylation and branching presented as the most prevalent post‐translational modifications of glycoproteins in patients with HCC compared to controls. Notably, glycomics‐based biomarkers may provide a clinical benefit for the diagnosis of early HCC, as several algorithms achieved AUCs between 0.92–0.97. However, these were based on single studies with limited sample sizes and should therefore be validated.ConclusionsAlterations in serum N‐glycomics, characterised by increased levels of fucosylation and branching, have potential as diagnostic biomarkers for HCC. Optimisation of study design, patient selection and analysing techniques are needed before clinical implementation will be possible.

Funder

Universitair Ziekenhuis Gent

Stichting Tegen Kanker

Kom op tegen Kanker

Publisher

Wiley

Subject

Pharmacology (medical),Gastroenterology,Hepatology

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