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dc.contributor.authorMüşteri Oltulu, Yasemin
dc.contributor.authorCoşkunpınar, Ender
dc.contributor.authorYıldız, Pınar
dc.contributor.authorAynacı, Engin
dc.contributor.authorKarimova, Ayla
dc.contributor.authorYaylım, İlhan
dc.date.accessioned2023-07-20T11:12:14Z
dc.date.available2023-07-20T11:12:14Z
dc.date.issued2023en_US
dc.identifier.citationMüşteri Oltulu, Y., Coşkunpınar, E., Yıldız, P., Aynacı, E., Karimova, A. ve Yaylım, İ. (2023). Investigation of miR221 and miR222 as biomarkers in non-small cell lung cancer. In Vivo, 37(4), 1603-1608. https://dx.doi.org/10.21873/invivo.13245en_US
dc.identifier.issn0258-851X
dc.identifier.issn1791-7549
dc.identifier.urihttps://dx.doi.org/10.21873/invivo.13245
dc.identifier.urihttps://hdl.handle.net/20.500.12511/11229
dc.description.abstractBackground/Aim: MicroRNAs (miRNA) are a class of small non-coding RNAs of 18-25 nucleotides, which regulate gene expression at the post-transcriptional level by disrupting or blocking translation of messenger RNA targets. Non-small cell lung cancer (NSCLC) represents approximately 85% of all lung cancers. Early and accurate diagnosis of the disease affects the probability of success of treatment. The purpose of this study was to investigate the expression levels of serum specific miRNA221 and miRNA222 as a biomarker in NSCLC. Materials and Methods: Thirty-two NSCLC cases and 30 healthy control cases that were diagnosed at Istanbul Yedikule Chest Diseases and Thoracic Surgery Training Hospital were included in this study. miRNAs were detected using miRNAspecific quantitative real-time-PCR. The relative expression of miRNAs was calculated using the 2-ccCt method. Results: miR221 and miR222 showed 1.46 and 1.63-fold higher expression in the samples from patients with NSCLC compared to controls, and the difference of expression was statistically significant for miR221 (p=0.000095) but not for miR222 (p=0.084470). In the presence of metastasis in NSCLC patients, miR221 levels were 2.33-fold higher compared to non-metastatic cases (p=0.014), and those of miR221 and miR222 were expressed 1.44 and 1.52-fold higher, respectively, in advanced stage compared to early stage (p=0.000387, p=0.000302). Conclusion: The levels of miR221 and miR222 in the serum of patients could be used as biomarkers for the diagnosis, treatment, and prognosis of NSCLC.en_US
dc.description.sponsorshipIstanbul Universityen_US
dc.language.isoengen_US
dc.publisherInternational Institute of Anticancer Researchen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectNSCLCen_US
dc.subjectBiomarkeren_US
dc.subjectGene Expressionen_US
dc.subjectmiR221en_US
dc.subjectmiR222en_US
dc.titleInvestigation of miR221 and miR222 as biomarkers in non-small cell lung canceren_US
dc.typearticleen_US
dc.relation.ispartofIn Vivoen_US
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Göğüs Hastalıkları Ana Bilim Dalıen_US
dc.identifier.volume37en_US
dc.identifier.issue4en_US
dc.identifier.startpage1603en_US
dc.identifier.endpage1608en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.21873/invivo.13245en_US
dc.institutionauthorAynacı, Engin
dc.identifier.wosqualityQ4en_US
dc.identifier.wos001023493400001en_US
dc.identifier.scopus2-s2.0-85164210534en_US
dc.identifier.pmid37369478en_US
dc.identifier.scopusqualityQ2en_US


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