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eNOS gene polymorphisms in paraffin-embedded tissues of prostate cancer patients.
Polat, Fikriye; Turaçlar, Nesrin; Yilmaz, Meral; Bingöl, Günsel; Cingilli Vural, Hasibe.
Afiliación
  • Polat F; Department of Primary Education, Faculty of Education, Elementary Sciences Education, Kocaeli University, Campus of Umuttepe, Kocaeli, Turkey.
  • Turaçlar N; Vocational School of Health Services, Selçuk University, Konya, Turkey.
  • Yilmaz M; Department of Research Centre, Faculty of Medicine, Cumhuriyet University, Sivas, Turkey.
  • Bingöl G; Biomedical Engineering, Faculty of Engineering and Natural Sciences, Yildirim Beyazit University, Ankara, Turkey.
  • Cingilli Vural H; Department of Biology, Molecular Biology, Selçuk University, Selçuklu, Konya, Turkey.
Turk J Med Sci ; 46(3): 673-9, 2016 Apr 19.
Article en En | MEDLINE | ID: mdl-27513240
BACKGROUND/AIM: The purpose of the present study was to investigate whether endothelial nitric oxide synthase (eNOS) gene polymorphisms play a role in prostate cancer (PCa). MATERIALS AND METHODS: We examined three eNOS gene polymorphisms (T-786C promoter region, G894T, and Intron 4 VNTR 4a/b) at extracted DNAs from 50 formalin-fixed paraffin-embedded tissues of PCa patients. For the controls, blood samples obtained from 50 healthy men were studied. Genotyping of molecular variants was performed by PCR-RFLP technique. RESULTS: We found that the TC genotype of the T-786C polymorphism was associated with PCa risk (OR: 3.325, CI: 1.350-8.188, P = 0.008). The eNOS G894T polymorphism was also associated with PCa. The frequency of the 894T allele was significantly higher in PCa patients. No association was identified between intron 4 VNTR polymorphism and PCa. CONCLUSION: We found significant differences in genotypic and allelic frequencies between PCa patients and controls for eNOS T-786C and G894T polymorphisms. The presence of the T-786C genotype and 894T allele in carriers increased the risk of PCa. No association was found between intron 4 VNTR polymorphism and PCa patients.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polimorfismo Genético Tipo de estudio: Prognostic_studies Límite: Humans / Male Idioma: En Revista: Turk J Med Sci Año: 2016 Tipo del documento: Article País de afiliación: Turquía Pais de publicación: Turquía

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polimorfismo Genético Tipo de estudio: Prognostic_studies Límite: Humans / Male Idioma: En Revista: Turk J Med Sci Año: 2016 Tipo del documento: Article País de afiliación: Turquía Pais de publicación: Turquía