Please use this identifier to cite or link to this item: https://doi.org/10.1038/srep36874
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dc.titleRs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk
dc.contributor.authorLiu, J
dc.contributor.authorLoncar, I
dc.contributor.authorColleé, J.M
dc.date.accessioned2020-10-21T08:17:41Z
dc.date.available2020-10-21T08:17:41Z
dc.date.issued2016
dc.identifier.citationLiu, J, Loncar, I, Colleé, J.M (2016). Rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk. Scientific Reports 6 : 36874. ScholarBank@NUS Repository. https://doi.org/10.1038/srep36874
dc.identifier.issn20452322
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/178759
dc.description.abstractNBS1, also known as NBN, plays an important role in maintaining genomic stability. Interestingly, rs2735383 G > C, located in a microRNA binding site in the 3?-untranslated region (UTR) of NBS1, was shown to be associated with increased susceptibility to lung and colorectal cancer. However, the relation between rs2735383 and susceptibility to breast cancer is not yet clear. Therefore, we genotyped rs2735383 in 1,170 familial non-BRCA1/2 breast cancer cases and 1,077 controls using PCR-based restriction fragment length polymorphism (RFLP-PCR) analysis, but found no association between rs2735383CC and breast cancer risk (OR = 1.214, 95% CI = 0.936-1.574, P = 0.144). Because we could not exclude a small effect size due to a limited sample size, we further analyzed imputed rs2735383 genotypes (r 2 > 0.999) of 47,640 breast cancer cases and 46,656 controls from the Breast Cancer Association Consortium (BCAC). However, rs2735383CC was not associated with overall breast cancer risk in European (OR = 1.014, 95% CI = 0.969-1.060, P = 0.556) nor in Asian women (OR = 0.998, 95% CI = 0.905-1.100, P = 0.961). Subgroup analyses by age, age at menarche, age at menopause, menopausal status, number of pregnancies, breast feeding, family history and receptor status also did not reveal a significant association. This study therefore does not support the involvement of the genotype at NBS1 rs2735383 in breast cancer susceptibility. © 2016 The Author(s).
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectBRCA1 protein
dc.subjectBRCA2 protein
dc.subjectcell cycle protein
dc.subjectmicroRNA
dc.subjectNBN protein, human
dc.subjectnuclear protein
dc.subject3' untranslated region
dc.subjectallele
dc.subjectbinding site
dc.subjectbreast tumor
dc.subjectfemale
dc.subjectgenetic predisposition
dc.subjectgenetics
dc.subjectgenotype
dc.subjecthuman
dc.subjectmetabolism
dc.subjectodds ratio
dc.subjectpathology
dc.subjectrisk factor
dc.subjectsingle nucleotide polymorphism
dc.subject3' Untranslated Regions
dc.subjectAlleles
dc.subjectBinding Sites
dc.subjectBRCA1 Protein
dc.subjectBRCA2 Protein
dc.subjectBreast Neoplasms
dc.subjectCell Cycle Proteins
dc.subjectFemale
dc.subjectGenetic Predisposition to Disease
dc.subjectGenotype
dc.subjectHumans
dc.subjectMicroRNAs
dc.subjectNuclear Proteins
dc.subjectOdds Ratio
dc.subjectPolymorphism, Single Nucleotide
dc.subjectRisk Factors
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.contributor.departmentSURGERY
dc.contributor.departmentPATHOLOGY
dc.description.doi10.1038/srep36874
dc.description.sourcetitleScientific Reports
dc.description.volume6
dc.description.page36874
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