Glycoprofiling of proteins as prostate cancer biomarkers: A multinational population study.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2024
Historique:
received: 14 07 2023
accepted: 27 02 2024
medline: 19 3 2024
pubmed: 19 3 2024
entrez: 18 3 2024
Statut: epublish

Résumé

The glycoprofiling of two proteins, the free form of the prostate-specific antigen (fPSA) and zinc-α-2-glycoprotein (ZA2G), was assessed to determine their suitability as prostate cancer (PCa) biomarkers. The glycoprofiling of proteins was performed by analysing changes in the glycan composition on fPSA and ZA2G using lectins (proteins that recognise glycans, i.e. complex carbohydrates). The specific glycoprofiling of the proteins was performed using magnetic beads (MBs) modified with horseradish peroxidase (HRP) and antibodies that selectively enriched fPSA or ZA2G from human serum samples. Subsequently, the antibody-captured glycoproteins were incubated on lectin-coated ELISA plates. In addition, a novel glycoprotein standard (GPS) was used to normalise the assay. The glycoprofiling of fPSA and ZA2G was performed in human serum samples obtained from men undergoing a prostate biopsy after an elevated serum PSA, and prostate cancer patients with or without prior therapy. The results are presented in the form of an ROC (Receiver Operating Curve). A DCA (Decision Curve Analysis) to evaluate the clinical performance and net benefit of fPSA glycan-based biomarkers was also performed. While the glycoprofiling of ZA2G showed little promise as a potential PCa biomarker, the glycoprofiling of fPSA would appear to have significant clinical potential. Hence, the GIA (Glycobiopsy ImmunoAssay) test integrates the glycoprofiling of fPSA (i.e. two glycan forms of fPSA). The GIA test could be used for early diagnoses of PCa (AUC = 0.83; n = 559 samples) with a potential for use in therapy-monitoring (AUC = 0.90; n = 176 samples). Moreover, the analysis of a subset of serum samples (n = 215) revealed that the GIA test (AUC = 0.81) outperformed the PHI (Prostate Health Index) test (AUC = 0.69) in discriminating between men with prostate cancer and those with benign serum PSA elevation.

Identifiants

pubmed: 38498504
doi: 10.1371/journal.pone.0300430
pii: PONE-D-23-22079
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0300430

Informations de copyright

Copyright: © 2024 Pinkeova et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Andrea Pinkeova (A)

Glycanostics, Ltd., Bratislava, Slovak Republic.
Institute of Chemistry, Bratislava, Slovak Republic.

Adela Tomikova (A)

Glycanostics, Ltd., Bratislava, Slovak Republic.

Aniko Bertokova (A)

Glycanostics, Ltd., Bratislava, Slovak Republic.

Eva Fabinyova (E)

Glycanostics, Ltd., Bratislava, Slovak Republic.

Radka Bartova (R)

Glycanostics, Ltd., Bratislava, Slovak Republic.

Eduard Jane (E)

Glycanostics, Ltd., Bratislava, Slovak Republic.
Institute of Chemistry, Bratislava, Slovak Republic.

Stefania Hroncekova (S)

Institute of Chemistry, Bratislava, Slovak Republic.

Karl-Dietrich Sievert (KD)

Klinikum Lippe - Clinic for Urology, Detmold, Germany.

Roman Sokol (R)

Private Urological Ambulance, Trencin, Slovak Republic.

Michal Jirasko (M)

Department of Pharmacology and Toxicology, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.

Radek Kucera (R)

Department of Pharmacology and Toxicology, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Department of Immunochemistry Diagnostics, University Hospital in Pilsen, Pilsen, Czech Republic.

Iris E Eder (IE)

Division of Experimental Urology, Department of Urology, Medical University Innsbruck, Innsbruck, Austria.

Wolfgang Horninger (W)

Division of Experimental Urology, Department of Urology, Medical University Innsbruck, Innsbruck, Austria.

Helmut Klocker (H)

Division of Experimental Urology, Department of Urology, Medical University Innsbruck, Innsbruck, Austria.

Petra Ďubjaková (P)

University Hospital Bratislava, Bratislava, Slovakia.

Juraj Fillo (J)

University Hospital Bratislava, Bratislava, Slovakia.

Tomas Bertok (T)

Glycanostics, Ltd., Bratislava, Slovak Republic.
Institute of Chemistry, Bratislava, Slovak Republic.

Jan Tkac (J)

Glycanostics, Ltd., Bratislava, Slovak Republic.
Institute of Chemistry, Bratislava, Slovak Republic.

Classifications MeSH