Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/2024
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dc.contributor.authorNikolić, Zorana Z.en_US
dc.contributor.authorSavić Pavićević, Dušanka Lj.en_US
dc.contributor.authorRomac, Stanka P.en_US
dc.contributor.authorBrajušković, Goran N.en_US
dc.date.accessioned2019-10-20T20:20:02Z-
dc.date.available2019-10-20T20:20:02Z-
dc.date.issued2015-02-
dc.identifier.issn1752-8054-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/2024-
dc.description.abstract© 2014 Wiley Periodicals, Inc. Several variants within gene-encoding endothelial isoform of nitric oxide synthase have been reported to confer prostate cancer (PCa) susceptibility and/or progression. Nevertheless, studies referring to this issue have yielded inconsistent results. In order to elucidate the involvement of these variants in prostate carcinogenesis, we have conducted a meta-analysis of previously published case-control and relevant case-only studies. Eleven studies comprising in total 3,806 cases and 4,466 controls were included in the meta-analysis which yielded evidence of association of rs2070744 (ORCC = 1.43, 95% CI 1.04-1.97; p = 0.03) and intron 4a/b variant (ORab+aa = 1.47, 95% CI 1.00-2.14; p = 0.05) with PCa risk under recessive and dominant model, respectively. Furthermore, PCa patients carrying 4a/b a allele were found to have an increased risk of cancer progression to a less differentiated form, characterized by a high Gleason score (OR = 2.29, 95% CI 1.51-3.49; p < 0.01) and to higher TNM stage (OR = 2.55, 95% CI 1.71-3.81; p < 0.01). These results support the involvement of NOS3 variants in molecular pathogenesis of PCa.en_US
dc.language.isoenen_US
dc.relation.ispartofClinical and Translational Scienceen_US
dc.subject4a/ben_US
dc.subjectMeta-analysisen_US
dc.subjectNOS3en_US
dc.subjectProstate canceren_US
dc.subjectRs1799983en_US
dc.subjectRs2070744en_US
dc.titleGenetic Variants within Endothelial Nitric Oxide Synthase Gene and Prostate Cancer: A Meta-Analysisen_US
dc.typeArticleen_US
dc.identifier.doi10.1111/cts.12203-
dc.identifier.pmid25164276-
dc.identifier.scopus2-s2.0-84922573938-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84922573938-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.grantfulltextrestricted-
item.openairetypeArticle-
item.languageiso639-1en-
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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