Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/2022
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dc.contributor.authorNikolić, Zorana Z.en_US
dc.contributor.authorSavić Pavićević, Dušanka Lj.en_US
dc.contributor.authorVukotić, Vinka D.en_US
dc.contributor.authorTomović, Saša M.en_US
dc.contributor.authorCerović, Snežana J.en_US
dc.contributor.authorFilipović, Natašaen_US
dc.contributor.authorRomac, Stanka P.en_US
dc.contributor.authorBrajušković, Goran N.en_US
dc.date.accessioned2019-10-20T20:13:28Z-
dc.date.available2019-10-20T20:13:28Z-
dc.date.issued2014-11-
dc.identifier.issn0957-5243-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/2022-
dc.description.abstract© 2014, Springer International Publishing Switzerland. Purpose: Two previous studies of association between rs2910164 in miR-146a gene and prostate cancer (PCa) risk have provided opposing results. Furthermore, no evidence of association of this SNP with standard prognostic parameters of PCa progression was obtained in mentioned studies. The main aim of this study was to evaluate the possible association between PCa onset and progression to a more aggressive form, since it has not been assessed in a population of European descent.Methods: In this study, 286 samples of peripheral blood were obtained from patients with PCa, while the control group comprised 199 volunteers derived from general population who gave samples of buccal swabs. For individuals diagnosed with PCa clinicopathological characteristics including serum prostate-specific antigen level at diagnosis, Gleason score (GS), and clinical stage were determined. Genotyping of rs2910164 was performed using Taqman®SNP Genotyping Assay. Analysis of SNP association was done using PLINK and SNPStats software.Results: rs2910164 showed no association with PCa risk. Nevertheless, heterozygous genotype was found to be associated with higher GS, as well as with the presence of distant metastases. rs2910164 was also shown to be associated with cancer aggressiveness (p = 0.0067; ORGC = 2.22, 95 %CI 1.24–3.97; ORCC = 0.47, 95 %CI 0.13–1.68).Conclusions: Our results show no evidence of association between rs2910164 and PCa risk in Serbian population. Conversely, this variant was found to be associated with PCa aggressiveness.en_US
dc.language.isoenen_US
dc.relation.ispartofCancer Causes and Controlen_US
dc.subjectAssociation studyen_US
dc.subjectmicroRNAen_US
dc.subjectmiR-146aen_US
dc.subjectProstate canceren_US
dc.subjectSingle-nucleotide polymorphismen_US
dc.titleAssociation between genetic variant in hsa-miR-146a gene and prostate cancer progression: evidence from Serbian populationen_US
dc.typeArticleen_US
dc.identifier.doi10.1007/s10552-014-0452-9-
dc.identifier.pmid25084752-
dc.identifier.scopus2-s2.0-84911953535-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84911953535-
item.fulltextWith Fulltext-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.grantfulltextrestricted-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptChair of Biochemistry and Molecular Biology-
crisitem.author.deptChair of Biochemistry and Molecular Biology-
crisitem.author.orcid0000-0002-2079-4077-
crisitem.author.orcid0000-0002-3935-6755-
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