Serum Insights: Leveraging the Power of miRNA Profiling as an Early Diagnostic Tool for Non-Small Cell Lung Cancer

dc.contributor.authorCharkiewicz Radoslaw
dc.contributor.authorSulewska Anetta
dc.contributor.authorMroz Robert
dc.contributor.authorCharkiewicz Alicja
dc.contributor.authorNaumnik Wojciech
dc.contributor.authorKraska Marcin
dc.contributor.authorGyenesei Attila
dc.contributor.authorGalik Bence
dc.contributor.authorJunttila Sini
dc.contributor.authorMiskiewicz Borys
dc.contributor.authorStec Rafal
dc.contributor.authorKarabowicz Piotr
dc.contributor.authorZawada Magdalena
dc.contributor.authorMiltyk Wojciech
dc.contributor.authorNiklinski Jacek
dc.contributor.organizationfi=Turun biotiedekeskus|en=Turku Bioscience Centre|
dc.contributor.organization-code1.2.246.10.2458963.20.18586209670
dc.converis.publication-id182031047
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/182031047
dc.date.accessioned2025-08-28T00:33:11Z
dc.date.available2025-08-28T00:33:11Z
dc.description.abstract<p>Non-small cell lung cancer is the predominant form of lung cancer and is associated with a poor prognosis. MiRNAs implicated in cancer initiation and progression can be easily detected in liquid biopsy samples and have the potential to serve as non-invasive biomarkers. In this study, we employed next-generation sequencing to globally profile miRNAs in serum samples from 71 early-stage NSCLC patients and 47 non-cancerous pulmonary condition patients. Preliminary analysis of differentially expressed miRNAs revealed 28 upregulated miRNAs in NSCLC compared to the control group. Functional enrichment analyses unveiled their involvement in NSCLC signaling pathways. Subsequently, we developed a gradient-boosting decision tree classifier based on 2588 miRNAs, which demonstrated high accuracy (0.837), sensitivity (0.806), and specificity (0.859) in effectively distinguishing NSCLC from non-cancerous individuals. Shapley Additive exPlanations analysis improved the model metrics by identifying the top 15 miRNAs with the strongest discriminatory value, yielding an AUC of 0.96 ± 0.04, accuracy of 0.896, sensitivity of 0.884, and specificity of 0.903. Our study establishes the potential utility of a non-invasive serum miRNA signature as a supportive tool for early detection of NSCLC while also shedding light on dysregulated miRNAs in NSCLC biology. For enhanced credibility and understanding, further validation in an independent cohort of patients is warranted.<br></p>
dc.identifier.eissn2072-6694
dc.identifier.jour-issn2072-6694
dc.identifier.olddbid205920
dc.identifier.oldhandle10024/188947
dc.identifier.urihttps://www.utupub.fi/handle/11111/36529
dc.identifier.urlhttps://www.mdpi.com/2072-6694/15/20/4910
dc.identifier.urnURN:NBN:fi-fe2025082791086
dc.language.isoen
dc.okm.affiliatedauthorJunttila, Sini
dc.okm.discipline3122 Cancersen_GB
dc.okm.discipline3122 Syöpätauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherMDPI
dc.publisher.countrySwitzerlanden_GB
dc.publisher.countrySveitsifi_FI
dc.publisher.country-codeCH
dc.relation.articlenumber4910
dc.relation.doi10.3390/cancers15204910
dc.relation.ispartofjournalCancers
dc.relation.issue20
dc.relation.volume15
dc.source.identifierhttps://www.utupub.fi/handle/10024/188947
dc.titleSerum Insights: Leveraging the Power of miRNA Profiling as an Early Diagnostic Tool for Non-Small Cell Lung Cancer
dc.year.issued2023

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