Your browser doesn't support javascript.
loading
RRM1, RRM2 and ERCC2 Gene Polymorphisms in Coronary Artery Disease.
Altinkilic, Emre Murat; Isbir, Selim; Gormus, Uzay; Yilmaz, Seda Gulec; Dalan, Altay Burak; Duman, Selvi; Isbir, Turgay.
Affiliation
  • Altinkilic EM; Department of Molecular Medicine, Institute of Health Sciences, Yeditepe University, Istanbul, Turkey.
  • Isbir S; Department of Cardiovascular Surgery, Marmara University Pendik Education and Research Hospital, Istanbul, Turkey.
  • Gormus U; Department of Biochemistry, Faculty of Medicine, Istanbul Bilim University, Istanbul, Turkey.
  • Yilmaz SG; Department of Molecular Medicine, Institute of Health Sciences, Yeditepe University, Istanbul, Turkey.
  • Dalan AB; Department of Biochemistry, Faculty of Medicine, Yeditepe University, Istanbul, Turkey.
  • Duman S; Department of Cardiovascular Surgery, Marmara University Pendik Education and Research Hospital, Istanbul, Turkey.
  • Isbir T; Department of Medical Biology, Faculty of Medicine, Yeditepe University, Istanbul, Turkey turgay.isbir@yeditepe.edu.tr tisbir@superonline.com.
In Vivo ; 30(5): 611-5, 2016.
Article in En | MEDLINE | ID: mdl-27566080
BACKGROUND/AIM: Coronary artery disease (CAD) is a chronic inflammatory disease seen as formation of atherosclerotic plaques (atheroma) in coronary arteries. Recent published papers show that DNA damage and repair mechanisms play a crucial role on the development and severity of atheromas. In this study, we investigated nucleotide excision repair (NER) pathway-related gene polymorphisms in atherosclerosis. XPD, encoded by ERCC2 gene, is an ATP-depended helicase enzyme involved in the NER pathway. Ribonucleotide reductase (RR) is a tetra meric enzyme, synthesizing deoxyribonucleotides from ribonucleotides for DNA synthesis. RR is encoded by the RRM1 and RRM2 genes, which are two subunits of RR enzyme. MATERIALS AND METHODS: DNA samples isolated from peripheral blood were genotyped with real-time polymerase chain reaction (RT-PCR) for RRM1 (rs12806698), RRM2(rs6859180) and ERCC2 (rs13181) genes. RESULTS: The frequency of the RRM1 AC heterozygote genotype was found to be significantly lower (odds ratio (OR)=0.369, 95% confidence interval (CI)=0.179-0.760; p=0.006), whereas the CC homozygote genotype was found to be significantly higher in patients compared to controls (OR=7.636, 95% CI=2.747-21.229; p=0.000). In addition, the RRM1 A allele was higher in control group (p=0.000, OR=0.131 95%CI=0.047-0.364). For the ERCC2 gene, GG genotype was significantly higher in control group (p=0.017, OR=0.387, 95%CI=0.175-0.152) and TT genotype (p=0.021) was higher in CAD group. TT genotype had a ~3-fold increased risk (OR=3.615, 95%CI=1.148-11.380) for CAD. Carrying T allele appears to be a risk factor for CAD (p=0.017, OR=2.586, 95%CI=1.173-5.699), while the G allele might be a risk-reducing factor (p=0.021, OR=0.277, 95%CI=0.088-0.871) for CAD. CONCLUSION: RRM1 and ERCC gene polymorphisms, having homozygous mutant genotype, might be a risk factor for CAD. RRM1 and ERCC wild type alleles are risk-reducing factor for CAD. Also, carrying RRM1 A allele might have a protective effect for smokers.
Subject(s)
Key words
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Ribonucleoside Diphosphate Reductase / Coronary Artery Disease / Tumor Suppressor Proteins / Xeroderma Pigmentosum Group D Protein Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: In Vivo Journal subject: NEOPLASIAS Year: 2016 Document type: Article Affiliation country: Turquía Country of publication: Grecia
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Ribonucleoside Diphosphate Reductase / Coronary Artery Disease / Tumor Suppressor Proteins / Xeroderma Pigmentosum Group D Protein Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: In Vivo Journal subject: NEOPLASIAS Year: 2016 Document type: Article Affiliation country: Turquía Country of publication: Grecia