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Title:Thymidine kinase as a biomarker of chemoresistance in epithelial ovarian cancer using the KELIM model
Authors:ID Lukanović, David (Author)
ID Osredkar, Joško (Author)
ID Škof, Erik (Author)
ID Cviič, Diana (Author)
ID Jerin, Aleš (Author)
ID Lešnik, Kaja (Author)
ID Matjašič, Miha (Author)
ID Meglič, Leon (Author)
Files:.pdf PDF - Presentation file, download (2,28 MB)
MD5: 354821780B8AECCBCB4EA984CDFB1CFF
 
URL URL - Source URL, visit https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2026.1617484/full
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo UKC LJ - Ljubljana University Medical Centre
Abstract:Background: Ovarian cancer (OC) remains the most lethal gynecological malignancy, with platinum sensitivity being a key determinant of treatment outcomes. The KELIM model, derived from CA-125 kinetics, is a promising biomarker for predicting chemosensitivity. Thymidine kinase 1 (TK1), a proliferation marker, has shown relevance in various cancers but its role in chemotherapy response for OC is unclear.Methods: In this retrospective study, we assessed the association between TK1 protein (TK1p) and enzymatic activity (TK1a) and chemosensitivity (KELIM), platinum-free interval (PFI), and chemotherapy response score (CRS) in 28 patients with epithelial OC treated with platinum-based chemotherapy. Biomarker dynamics were measured at multiple timepoints. KELIM was calculated using CA-125 kinetics; relationships with CRS and PFI were evaluated.Results: KELIM demonstrated robust predictive performance (correlating with favorable CRS [rho = 0.731, p = 0.011] and longer PFI [rho = 0.437, p = 0.007]). TK1p and TK1a showed no significant correlations with KELIM, PFI, or CRS. ROC analysis for preoperative TK1p yielded an AUC of 0.6941, indicating moderate discriminative potential. TK1a increased postoperatively but lacked predictive value for chemoresistance.Conclusion: Our findings reinforce the value of KELIM as a reliable predictor of platinum sensitivity in OC. TK1 dynamics reflect tumor proliferation but did not significantly predict chemotherapy response. Larger cohorts and further research are required to explore whether TK1 can complement established biomarkers.
Keywords:biomarker, CA-125, chemoresistance, epithelial ovarian cancer, KELIM, ovarian cancer, thymidine kinase
Publication status:Published
Publication version:Version of Record
Year of publishing:2026
Number of pages:11 str.
Numbering:Vol. 17, [article no.] ǂ1617484
PID:20.500.12556/DiRROS-29262 New window
UDC:616-006:618.11
ISSN on article:1663-9812
DOI:10.3389/fphar.2026.1617484 New window
COBISS.SI-ID:276854531 New window
Note:Nasl. z nasl. zaslona; Opis vira z dne 4. 5. 2026;
Publication date in DiRROS:05.05.2026
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Downloads:36
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Record is a part of a journal

Title:Frontiers in pharmacology
Shortened title:Front Pharmacol
Publisher:Frontiers Media
ISSN:1663-9812
COBISS.SI-ID:29551833 New window

Document is financed by a project

Funder:Other - Other funder or multiple funders
Funding programme:Univerzitetni klinični center Ljubljana
Project number:20190069
Name:Biomarkerji v diagnostiki raka trebušne slinavke in vpliv različnih polimorfizmov na uspešnost

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

Secondary language

Language:Slovenian
Keywords:biomarkerji, CA-125, kemorezistentnost, epitelijski rak jajčnikov, KELIM, rak jajčnikov, timidin kinaza


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