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Genetic Variations of DNA Repair Genes in Breast Cancer

dc.contributor.authorOzgoz, Asuman
dc.contributor.authorSamli, Hale
dc.contributor.authorOzturk, Kuyas Hekimler
dc.contributor.authorIcduygu, Fadime Mutlu
dc.contributor.authorBaskan, Zuhal
dc.contributor.authorBacaksiz, Mehmet
dc.contributor.authorYukselturk, Aysegul
dc.date.accessioned2026-01-03T10:11:40Z
dc.date.issued2017-10-05
dc.description.abstractGenetic variations in DNA repair genes may affect DNA repair capacity therefore increase risk for cancer. In our study, we evaluted the relation between DNA repair gene polymorphisms XRCC1 rs1799782, rs25487, rs25489; XPC rs2228000, rs2228001; XPD rs1799793, rs13181; XRCC3 rs861539; RAD51B rs10483813, rs1314913 and breast cancer risk for 202 Turkish cases in total, in which 102 patients with breast cancer and 100 controls. Genotyping of the DNA samples was carried out by multiplex PCR and matrix-assisted laser desorption/ionization mass spectrometry with time of flight measurement (MALDI-TOF) using Sequenom MassARRAY 4 analyzer. Genotype and allele distributions were calculated between the groups. Odds ratios (ORs) and 95% confidence intervals (CIs) were reported. rs25487 AA genotype and A allele was found to be increased in the control group (respectively, OR 0.16 95% CI 0.02-1.06, p = 0.058; OR 1.55, 95% CI 1.01-2.36, p = 0.043) and rs861539 T allele was found to be decreased in the patient group (OR 1.53, 95% CI 1.01-2.30, p = 0.049). No association with breast cancer was found for the remaining SNPs. Our findings suggest that XRCC1 rs25487 AA genotype and A allele, XRCC3 rs861539 T allele may have protective effects in breast cancer for Turkish population.
dc.description.urihttps://doi.org/10.1007/s12253-017-0322-3
dc.description.urihttps://pubmed.ncbi.nlm.nih.gov/28983784
dc.description.urihttps://dx.doi.org/10.1007/s12253-017-0322-3
dc.description.urihttps://avesis.uludag.edu.tr/publication/details/28216856-0b74-432c-82fd-55fc73c34bd7/oai
dc.description.urihttps://hdl.handle.net/20.500.12697/2934
dc.description.urihttps://doi.org/https://doi.org/10.1007/s12253-017-0322-3
dc.identifier.doi10.1007/s12253-017-0322-3
dc.identifier.eissn1532-2807
dc.identifier.endpage114
dc.identifier.issn1219-4956
dc.identifier.openairedoi_dedup___::b32902f9b3a9b68f7d2db6cef416da31
dc.identifier.pubmed28983784
dc.identifier.scopus2-s2.0-85030717744
dc.identifier.startpage107
dc.identifier.urihttps://hdl.handle.net/20.500.12597/36547
dc.identifier.volume25
dc.identifier.wos000456915500012
dc.language.isoeng
dc.publisherSpringer Science and Business Media LLC
dc.relation.ispartofPathology & Oncology Research
dc.rightsOPEN
dc.subjectDNA Repair
dc.subjectGenotype
dc.subjectBreast Neoplasms
dc.subjectMiddle Aged
dc.subjectPrognosis
dc.subjectPolymorphism, Single Nucleotide
dc.subjectGene Expression Regulation, Neoplastic
dc.subjectDNA Repair Enzymes
dc.subjectCase-Control Studies
dc.subjectLymphatic Metastasis
dc.subjectBreast Cancer
dc.subjectBiomarkers, Tumor
dc.subjectHumans
dc.subjectFemale
dc.subjectGenetic Predisposition to Disease
dc.subjectPolymorphism
dc.subjectDNA Damage
dc.subjectFollow-Up Studies
dc.subject.sdg3. Good health
dc.titleGenetic Variations of DNA Repair Genes in Breast Cancer
dc.typeArticle
dspace.entity.typePublication
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No association with breast cancer was found for the remaining SNPs. 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