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dc.contributor.authorBeysel, Selvihan
dc.contributor.authorEyerci, Nilnur
dc.contributor.authorAlparslan Pınarlı, Ferda
dc.contributor.authorApaydın, Mahmut
dc.contributor.authorKızılgül, Muhammed
dc.contributor.authorÇalışkan, Mustafa
dc.contributor.authorÖzçelik, Özgür
dc.contributor.authorKan, Seyfullah
dc.contributor.authorÇakal, Erman
dc.date.accessioned2021-05-05T22:11:54Z
dc.date.available2021-05-05T22:11:54Z
dc.date.issued2018
dc.identifier.issn1010-4283
dc.identifier.urihttps://doi.org/10.1177/1010428318811766
dc.identifier.urihttps://hdl.handle.net/20.500.12933/228
dc.descriptionPubMed: 30486759en_US
dc.description2-s2.0-85057533408en_US
dc.description.abstractThis is the first study to investigate the effect of vitamin D receptor (VDR) gene single-nucleotide polymorphisms on the clinicopathologic features of papillary thyroid cancer in Turkey. A total of 165 patients with papillary thyroid cancer and 172 controls were included in this case–control study. VDR gene single-nucleotide polymorphisms FokI (rs2228570), BsmI (rs1544410), ApaI (rs7975232), and TaqI (rs731236) were evaluated using reverse-transcription polymerase chain reaction. VDR gene polymorphisms BsmI, ApaI, and TaqI did not differ between the papillary thyroid cancer group and control group (p > 0.05, each). BsmI, ApaI, and TaqI were not associated with papillary thyroid cancer risk. The VDR gene FokI CT/TT genotype was associated with an increased papillary thyroid cancer risk (CT vs CC: odds ratio = 1.71, 95% confidence interval = 1.15–2.76, p = 0.028; TT vs CC: odds ratio = 2.44, 95% confidence interval = 1.29–4.62, p = 0.005; CT/TT vs CC: odds ratio = 1.88, 95% confidence interval = 1.20–2.96, p = 0.006; CT/CC vs TT: odds ratio = 1.80, 95% confidence interval = 1.05–3.20, p = 0.041). VDR gene polymorphisms were not in linkage disequilibrium. The FokI TT genotype was associated with having T3 and T4, stage III/IV, extra-thyroidal invasion. The FokI CT/TT or TT genotype was associated with developing N1 status, multifocality, tumor size ?10 mm, and treatment with radioiodine therapy. Persistence/recurrence did not differ between the FokI genotypes. Carriers of the FokI T allele were at an increased risk of more advanced tumor-node-metastasis stage, greater tumor size, multifocality, and extra-thyroidal invasion of papillary thyroid cancer compared with the CC genotype. VDR gene FokI T allele and TT genotype correlated with aggressiveness of papillary thyroid cancer; thus, FokI could be useful as a poor prognostic factor to assess the high risk of papillary thyroid cancer. © The Author(s) 2018.en_US
dc.language.isoengen_US
dc.publisherSAGE Publications Ltden_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectFokI polymorphismen_US
dc.subjectpapillary thyroid canceren_US
dc.subjectVDR geneen_US
dc.titleVDR gene FokI polymorphism as a poor prognostic factor for papillary thyroid canceren_US
dc.typearticleen_US
dc.departmentAFSÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, İç Hastalıkları Ana Bilim Dalı
dc.contributor.institutionauthorBeysel, Selvihan
dc.identifier.doi10.1177/1010428318811766
dc.identifier.volume40en_US
dc.identifier.issue11en_US
dc.relation.journalTumor Biologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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