dc.contributor.author | Soleimani, Z | |
dc.contributor.author | Kheirkhah, D | |
dc.contributor.author | Sharif, MR | |
dc.contributor.author | Sharif, A | |
dc.contributor.author | Karimian, M | |
dc.contributor.author | Aftabi, Y | |
dc.date.accessioned | 2018-08-26T08:36:17Z | |
dc.date.available | 2018-08-26T08:36:17Z | |
dc.date.issued | 2017 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/52727 | |
dc.description.abstract | Cyclin 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.iso | English | |
dc.relation.ispartof | Pathology and Oncology Research | |
dc.subject | adenine | |
dc.subject | guanine | |
dc.subject | messenger RNA | |
dc.subject | CCND1 protein, human | |
dc.subject | cyclin D1 | |
dc.subject | adult | |
dc.subject | allele | |
dc.subject | Article | |
dc.subject | breast cancer | |
dc.subject | breast carcinogenesis | |
dc.subject | case control study | |
dc.subject | CCND1 gene | |
dc.subject | computer model | |
dc.subject | controlled study | |
dc.subject | female | |
dc.subject | gene | |
dc.subject | genetic association | |
dc.subject | genotype | |
dc.subject | human | |
dc.subject | major clinical study | |
dc.subject | RNA splicing | |
dc.subject | RNA structure | |
dc.subject | single nucleotide polymorphism | |
dc.subject | systematic review | |
dc.subject | breast tumor | |
dc.subject | genetic predisposition | |
dc.subject | genetics | |
dc.subject | meta analysis | |
dc.subject | middle aged | |
dc.subject | restriction fragment length polymorphism | |
dc.subject | risk factor | |
dc.subject | single nucleotide polymorphism | |
dc.subject | Alleles | |
dc.subject | Breast Neoplasms | |
dc.subject | Case-Control Studies | |
dc.subject | Cyclin D1 | |
dc.subject | Female | |
dc.subject | Genetic Predisposition to Disease | |
dc.subject | Genotype | |
dc.subject | Humans | |
dc.subject | Middle Aged | |
dc.subject | Polymorphism, Restriction Fragment Length | |
dc.subject | Polymorphism, Single Nucleotide | |
dc.subject | Risk Factors | |
dc.title | Association of CCND1 Gene c.870G>A Polymorphism with Breast Cancer Risk: A Case-ControlStudy and a Meta-Analysis | |
dc.type | Article | |
dc.citation.volume | 23 | |
dc.citation.issue | 3 | |
dc.citation.spage | 621 | |
dc.citation.epage | 631 | |
dc.citation.index | Scopus | |
dc.identifier.DOI | https://doi.org/10.1007/s12253-016-0165-3 | |