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Association of vitamin D receptor polymorphism [VDR rs 2238136] with colorectal cancer
Journal of Kerman University of Medical Sciences. 2012; 19 (1): 1-8
Dans Persan | IMEMR | ID: emr-137416
ABSTRACT
Many studies have demonstrated that Vitamin D has an important role in cell growth and proliferation and vitamin D receptor polymorphism has significant relationship with colorectal cancer [CRC]. The aim of this study was to assess the incidence of VDR rs 2238136 polymorphism in Iranian population and to investigate the relationship between this single nucleotide polymorphism [SNP] and increased risk of CRC. In this case-control study, genotyping of vitamin D receptor gene polymorphism [VDR rs2238136] was determined in a series of 112 colorectal cancer patients and 112 controls by using polymerase chain reaction and restriction fragment length polymorphism genotyping assays [PCR-RFLP]. Statistical analysis was done through SPSS 16. VDR polymorphism [rs 2238136] had no significant relationship with CRC risk. The result of statistical analysis for the genotype AG compared with GG was OR=0. 59, CI=0.33-1.03 and for AA versus GG was OR=0.8, Ct=0.29-2.17. Incidence of mutant allele in patients and controls did not show significant difference [OR=0.74, CI=0.49 -1.13]. These findings suggest that VDR [rs 2238136] is not associated with increased risk of CRC. Moreover age, sex and smoking are not predisposing factors for increased risk of CRC
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Indice: Méditerranée orientale Sujet Principal: Polymorphisme génétique / Vitamine D / Polymorphisme de restriction / Tumeurs colorectales / Études cas-témoins / Réaction de polymérisation en chaîne / Facteurs de risque / Prédisposition génétique à une maladie / Génotype Limites du sujet: Humains langue: Persan Texte intégral: J. Kerman Univ. Med. Sci. Année: 2012

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Recherche sur Google
Indice: Méditerranée orientale Sujet Principal: Polymorphisme génétique / Vitamine D / Polymorphisme de restriction / Tumeurs colorectales / Études cas-témoins / Réaction de polymérisation en chaîne / Facteurs de risque / Prédisposition génétique à une maladie / Génotype Limites du sujet: Humains langue: Persan Texte intégral: J. Kerman Univ. Med. Sci. Année: 2012