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Genetic polymorphisms of vitamin D receptor (VDR), CYP27B1 and CYP24A1 genes and the risk of colorectal cancer.
Vidigal, Verônica Marques; Silva, Tiago Donizetti; de Oliveira, Juliana; Pimenta, Célia Aparecida Marques; Felipe, Aledson Vitor; Forones, Nora Manoukian.
Afiliação
  • Vidigal VM; Oncology Division, Gastroenterology Department, Universidade Federal de São Paulo, São Paulo - Brazil.
  • Silva TD; Oncology Division, Gastroenterology Department, Universidade Federal de São Paulo, São Paulo - Brazil.
  • de Oliveira J; Oncology Division, Gastroenterology Department, Universidade Federal de São Paulo, São Paulo - Brazil.
  • Pimenta CAM; Oncology Division, Gastroenterology Department, Universidade Federal de São Paulo, São Paulo - Brazil.
  • Felipe AV; Oncology Division, Gastroenterology Department, Universidade Federal de São Paulo, São Paulo - Brazil.
  • Forones NM; Oncology Division, Gastroenterology Department, Universidade Federal de São Paulo, São Paulo - Brazil.
Int J Biol Markers ; 32(2): e224-e230, 2017 May 04.
Article em En | MEDLINE | ID: mdl-28009432
INTRODUCTION: Vitamin D receptor (VDR) and proteins encoded by the genes CYP27B2 and CYP24A1 involved in the production and inactivation of vitamin D can influence vitamin D and the susceptibility to colorectal cancer (CRC). The objective of this study was to investigate the relationship between the risk of CRC and polymorphisms in VDR, CYP27B1 and CYP24A1, lifestyle and dietary habits. METHODS: The study included 152 patients with CRC and 321 controls. All participants answered a questionnaire on their dietary habits, alcohol consumption and smoking habits. DNA was extracted from peripheral blood. Polymorphisms of BsmI and ApaI were identified by performing PCR-RFLP. Identification of CYP24A1 (rs6013897, rs158552 and rs17217119) and CYP27B1 (rs10877012) polymorphisms was performed by gene sequencing. RESULTS: Smoking, alcohol use, and low or no consumption of fruit, cereals and dairy products were associated with an increased risk of CRC. A heterozygous genotype Aa or an association genotype aa + Aa of the VDR ApaI polymorphism increased the risk of CRC. The VDR BsmI polymorphism was not significantly associated with the risk of CRC. Multivariate analysis showed that heterozygous and association genotype AT + AA of the rs6013897 polymorphism, genotype CT of the rs158552 polymorphism, association genotype CT + CC and genotypes AA and GG of the rs17217119 polymorphism of CYP24A1, and heterozygous genotype GT and association genotype GT + TT of the rs10877012 polymorphism in CYP27B1 were associated with a higher risk of CRC. CONCLUSIONS: Dietary habits, lifestyle, and polymorphisms in VDR (ApaI), CYP24A1 (rs6013897, rs158552, rs17217119) and CYP27B1 (rs10877012) were associated with a higher risk of CRC.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Receptores de Calcitriol / Vitamina D3 24-Hidroxilase / 25-Hidroxivitamina D3 1-alfa-Hidroxilase Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Receptores de Calcitriol / Vitamina D3 24-Hidroxilase / 25-Hidroxivitamina D3 1-alfa-Hidroxilase Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article