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

dc.contributor.author Turk, Okan
dc.contributor.author Demirel, Nail
dc.contributor.author Yaltirik, Cumhur Kaan
dc.contributor.author Kaya, Mustafa
dc.contributor.author Sahin, Omer Faruk
dc.contributor.author Yilmaz, Seda Guelec
dc.contributor.author Isbir, Turgay
dc.date.accessioned 2024-05-25T11:37:47Z
dc.date.available 2024-05-25T11:37:47Z
dc.date.issued 2024
dc.description kaya, mustafa/0000-0001-5548-4944 en_US
dc.description.abstract Background/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.citationcount 0
dc.identifier.doi 10.21873/invivo.13485
dc.identifier.issn 0258-851X
dc.identifier.issn 1791-7549
dc.identifier.scopus 2-s2.0-85186742393
dc.identifier.uri https://doi.org/10.21873/invivo.13485
dc.identifier.uri https://hdl.handle.net/20.500.14517/1218
dc.language.iso en
dc.publisher int inst Anticancer Research en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject miRNA-17 en_US
dc.subject glial tumors en_US
dc.subject cerebral metastases en_US
dc.subject molecular pathogenesis en_US
dc.title Unraveling the Impact of<i> miRNA-17</i> in Glial Tumors and Cerebral Metastases: A Step Towards Enhanced Diagnosis and Prognosis en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id kaya, mustafa/0000-0001-5548-4944
gdc.author.institutional Akdeniz F.T.
gdc.author.scopusid 57190660302
gdc.author.scopusid 57199176420
gdc.author.scopusid 57193702082
gdc.author.scopusid 57194435382
gdc.author.scopusid 58920368400
gdc.author.scopusid 56644016600
gdc.author.scopusid 57565083500
gdc.author.wosid kaya, mustafa/GLQ-8341-2022
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.description.department Okan University en_US
gdc.description.departmenttemp [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, Turkiye en_US
gdc.description.endpage 656 en_US
gdc.description.issue 2 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q3
gdc.description.startpage 652 en_US
gdc.description.volume 38 en_US
gdc.description.wosquality Q3
gdc.identifier.pmid 38418125
gdc.identifier.wos WOS:001179422300003
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed
gdc.scopus.citedcount 1
gdc.wos.citedcount 1

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