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dc.contributor.authorSoleimani, Z
dc.contributor.authorKheirkhah, D
dc.contributor.authorSharif, MR
dc.contributor.authorSharif, A
dc.contributor.authorKarimian, M
dc.contributor.authorAftabi, Y
dc.date.accessioned2018-08-26T08:36:17Z
dc.date.available2018-08-26T08:36:17Z
dc.date.issued2017
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/52727
dc.description.abstractCyclin D1 (CCND1) plays an essential role in regulating the progress of the cell cycle from G1 to S phase. There is a common c.870G>A polymorphism in the CCND1 gene. The aim of this study was to investigate the association of CCND1 gene c.870G>A polymorphism with breast cancer risk in a case-control study, which followed by a meta-analysis and an in silico analysis. Three hundred and thirty-five subjects composed of 174 women with breast cancer and 161 healthy controls were included in the case-control study. CCND1 gene c.870G>A genotyping was performed by PCR-RFLP. Meta-analysis was done for 14 studies composed of 7281 cases and 6820 controls. Some bioinformatics tools were applied to investigate the effects of c.870G>A on the mRNA splicing and structure. Our data obtained from case-control study revealed that GA genotype (OR: 1.89, 95%CI: 1.12-3.17, pآ =آ 0.017), AA genotype (OR: 1.95, 95%CI: 1.08-3.53, pآ =آ 0.027), and A allele (OR: 1.44, 95%CI: 1.06-1.95, pآ =آ 0.019) were significantly associated with breast cancer risk. The results of meta-analysis showed a significant association between CCND1 c.870G>A polymorphism and breast cancer risk, especially in Caucasian population. In silico analysis revealed that c.870G>A transition affect CCND1 mRNA splicing and secondary structure. é 2016, Ar?nyi Lajos Foundation.
dc.language.isoEnglish
dc.relation.ispartofPathology and Oncology Research
dc.subjectadenine
dc.subjectguanine
dc.subjectmessenger RNA
dc.subjectCCND1 protein, human
dc.subjectcyclin D1
dc.subjectadult
dc.subjectallele
dc.subjectArticle
dc.subjectbreast cancer
dc.subjectbreast carcinogenesis
dc.subjectcase control study
dc.subjectCCND1 gene
dc.subjectcomputer model
dc.subjectcontrolled study
dc.subjectfemale
dc.subjectgene
dc.subjectgenetic association
dc.subjectgenotype
dc.subjecthuman
dc.subjectmajor clinical study
dc.subjectRNA splicing
dc.subjectRNA structure
dc.subjectsingle nucleotide polymorphism
dc.subjectsystematic review
dc.subjectbreast tumor
dc.subjectgenetic predisposition
dc.subjectgenetics
dc.subjectmeta analysis
dc.subjectmiddle aged
dc.subjectrestriction fragment length polymorphism
dc.subjectrisk factor
dc.subjectsingle nucleotide polymorphism
dc.subjectAlleles
dc.subjectBreast Neoplasms
dc.subjectCase-Control Studies
dc.subjectCyclin D1
dc.subjectFemale
dc.subjectGenetic Predisposition to Disease
dc.subjectGenotype
dc.subjectHumans
dc.subjectMiddle Aged
dc.subjectPolymorphism, Restriction Fragment Length
dc.subjectPolymorphism, Single Nucleotide
dc.subjectRisk Factors
dc.titleAssociation of CCND1 Gene c.870G>A Polymorphism with Breast Cancer Risk: A Case-ControlStudy and a Meta-Analysis
dc.typeArticle
dc.citation.volume23
dc.citation.issue3
dc.citation.spage621
dc.citation.epage631
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.1007/s12253-016-0165-3


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