Unraveling the Impact of<i> miRNA-17</i> in Glial Tumors and Cerebral Metastases: A Step Towards Enhanced Diagnosis and Prognosis

dc.authoridkaya, mustafa/0000-0001-5548-4944
dc.authorscopusid57190660302
dc.authorscopusid57199176420
dc.authorscopusid57193702082
dc.authorscopusid57194435382
dc.authorscopusid58920368400
dc.authorscopusid56644016600
dc.authorscopusid57565083500
dc.authorwosidkaya, mustafa/GLQ-8341-2022
dc.contributor.authorTurk, Okan
dc.contributor.authorDemirel, Nail
dc.contributor.authorYaltirik, Cumhur Kaan
dc.contributor.authorKaya, Mustafa
dc.contributor.authorSahin, Omer Faruk
dc.contributor.authorYilmaz, Seda Guelec
dc.contributor.authorIsbir, Turgay
dc.contributor.otherGenetik ve Biyomühendislik / Genetic and Bio-Engineering
dc.date.accessioned2024-05-25T11:37:47Z
dc.date.available2024-05-25T11:37:47Z
dc.date.issued2024
dc.departmentOkan Universityen_US
dc.department-temp[Turk, Okan; Demirel, Nail] Univ Hlth Sci, Istanbul Training & Res Hosp, Dept Neurosurg, Org Abdurrahman Nafiz Gurman Cd 24, TR-34098 Istanbul, Turkiye; [Akdeniz, Fatma Tuba] Univ Hlth Sci, Umraniye Training & Res Hosp, Dept Neurosurg, Istanbul, Turkiye; [Kaya, Mustafa] Sakarya Univ, Sakarya Training & Res Hosp, Dept Neurosurg, Sakarya, Turkiye; [Sahin, Omer Faruk] Ordu Training & Res Hosp, Dept Neurosurg, Ordu, Turkiye; [Yilmaz, Seda Guelec] Yeditepe Univ, Fac Med, Dept Med Biol, Istanbul, Turkiye; [Akdeniz, Fatma Tuba] Okan Univ, Fac Engn & Nat Sci, Dept Genet & Bioengn, Istanbul, Turkiye; [Isbir, Turgay] Yeditepe Univ, Inst Hlth Sci, Dept Mol Med, Istanbul, Turkiyeen_US
dc.descriptionkaya, mustafa/0000-0001-5548-4944en_US
dc.description.abstractBackground/Aim: MicroRNAs (miRNAs) have been identified as key regulators in various cancer types, including brain tumors. This study aimed to investigate the differential expression of miRNA-17 in glial tumors, cerebral metastases, and normal glial tissues. Materials and Methods: A total of 42 patients were included in this cross-sectional study. Tissue samples were obtained from patients with glial tumors or cerebral metastases and from normal glial tissues. miRNA-17 expression levels were computed by using real-time polymerase chain reaction. Receiver operating characteristics analysis was used to determine the predictive potential of miRNA-17. Results: In this study, we demonstrated a statistically significant difference in miRNA-17 expression levels between glial tumors and the control group (p=0.001), with higher miRNA-17 expression observed in glial tumors. Similarly, there was statistically higher miRNA-17 expression in metastatic cases compared with the control group (p=0.007). Conclusion: These findings suggest miRNA-17 might be a potential biomarker for differentiating glial tumors and cerebral metastases from normal glial tissue, although further research is necessary to validate these findings and investigate the potential role of miRNA-17 in the pathogenesis of these brain tumors.en_US
dc.identifier.citation0
dc.identifier.doi10.21873/invivo.13485
dc.identifier.endpage656en_US
dc.identifier.issn0258-851X
dc.identifier.issn1791-7549
dc.identifier.issue2en_US
dc.identifier.pmid38418125
dc.identifier.scopus2-s2.0-85186742393
dc.identifier.scopusqualityQ3
dc.identifier.startpage652en_US
dc.identifier.urihttps://doi.org/10.21873/invivo.13485
dc.identifier.urihttps://hdl.handle.net/20.500.14517/1218
dc.identifier.volume38en_US
dc.identifier.wosWOS:001179422300003
dc.identifier.wosqualityQ4
dc.institutionauthorAkdeniz F.T.
dc.institutionauthorFatma Tuba, Akdeniz
dc.language.isoen
dc.publisherint inst Anticancer Researchen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectmiRNA-17en_US
dc.subjectglial tumorsen_US
dc.subjectcerebral metastasesen_US
dc.subjectmolecular pathogenesisen_US
dc.titleUnraveling the Impact of<i> miRNA-17</i> in Glial Tumors and Cerebral Metastases: A Step Towards Enhanced Diagnosis and Prognosisen_US
dc.typeArticleen_US
dspace.entity.typePublication
relation.isAuthorOfPublication7ae75335-993a-40c1-b33e-6207ca2b7989
relation.isAuthorOfPublication.latestForDiscovery7ae75335-993a-40c1-b33e-6207ca2b7989
relation.isOrgUnitOfPublication2b8689c6-2a28-45db-b81c-7f828c944e77
relation.isOrgUnitOfPublication.latestForDiscovery2b8689c6-2a28-45db-b81c-7f828c944e77

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