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dc.contributor.authorBardakci, F.
dc.contributor.authorArslan, S.
dc.contributor.authorBardakci, S.
dc.contributor.authorBinatli, A. O.
dc.contributor.authorBudak, M.
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T10:15:44Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T10:15:44Z
dc.date.issued2008
dc.identifier.issn0171-5216
dc.identifier.urihttps://dx.doi.org/10.1007/s00432-007-0256-3
dc.identifier.urihttps://hdl.handle.net/20.500.12418/10462
dc.descriptionWOS: 000250722100014en_US
dc.descriptionPubMed ID: 17605044en_US
dc.description.abstractPurpose Sulfotransferase 1A1 is a member of sulfotransferase family that plays an important role in the biotransformation of numerous carcinogenic and mutagenic compounds through sulfation. The present study has investigated the association between SULT1A1 polymorphism and primary brain tumor incidence. Methods SULT1A1 genotypes were successfully detected using the PCR-RFLP assay in 60 primary brain tumor patients and 156 hospital-based healthy control individuals with no history of cancer or precancerous disorder. Results There was a significant difference in genotypes distribution (GG vs. GA + AA) between brain tumor patients (GG genotype frequency = 48.3%) and control population (GG genotype frequency = 65.4%; OR = 2.019, 95% CI = 1.103-3.695; P = 0.022). In order to determine the association between SULT1A1 polymorphism and specific types of brain tumors, the patients were classified according to the type of brain tumors they suffer from: glial and non-glial. Results of the statistical analyses of each group of patients in comparison with the control individuals showed a significant difference only between SULT1A1 polymorphism and non-glial brain tumors (OR = 2.615; 95% CI = 1.192 5.739; P = 0.014) but glial tumors (OR = 1.535; 95% CI = 0.688-3.425; P = 0.293). When non-glial tumors were classifed as meningiomal and others (pituitary adenoma, craniopharyngioma, acoustic neuroma and hemangioblastoma), statistical analysis showed that this significance is only due to the meningiomal tumors (OR = 3.238; CI = 1.205-8.704; P = 0.015). We also estimated a reduced risk of brain tumor in non-smokers (OR = 1.700; CI = 0.800-3.615) in comparison to smokers (OR = 2.773; CI = 0.993-7.749), but this was not statistically significant. Conclusion Our findings have suggested that there was a significant association between brain tumor and SULT1A1*2 2 allele (A allele that is also known as His allele) and this allele is an important risk factor in the development of meningiomal brain tumors.en_US
dc.language.isoengen_US
dc.publisherSPRINGERen_US
dc.relation.isversionof10.1007/s00432-007-0256-3en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectsulfotranferaseen_US
dc.subjectepidemiologyen_US
dc.subjectcanceren_US
dc.subjectpolymorphismen_US
dc.subjectsulfationen_US
dc.titleSulfotransferase 1A1 (SULT1A1) polymorphism and susceptibility to primary brain tumorsen_US
dc.typearticleen_US
dc.relation.journalJOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGYen_US
dc.contributor.departmentAdnan Menderes Univ, Fac Sci & Literature, Dept Biol, TR-09100 Aydin, Turkey -- Cumhuriyet Univ, Fac Sci & Literature, Dept Mol Biol & Genet, TR-58140 Sivas, Turkey -- Tepecik Hosp, Dept Neurosurg, Izmir, Turkey -- Cumhuriyet Univ, Fac Sci & Literature, Dept Biol, TR-58140 Sivas, Turkeyen_US
dc.contributor.authorIDBudak, Mahir -- 0000-0001-5610-486Xen_US
dc.identifier.volume134en_US
dc.identifier.issue1en_US
dc.identifier.endpage114en_US
dc.identifier.startpage109en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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