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Allele frequencies of T-34C CYP17 and A66G MTRR polymorphisms in breast cancer samples and the correlation with clinicopathological data can contribute to the prognosis and knowledge of the genetic profile of a population. In this study, was analized the association of T-34C CYP17 and A66G MTRR polymorphisms with clinicopathological data in 82 samples of invasive ductal breast carcinoma in the Southwest region of Bahia. PCR-RFLP was used to determine the genotypes for A66G MTRR and T-34C CYP17 polymorphisms. The allele frequency was 0.369 and 0.631 for A66G MTRR; 0.672 and 0.328 for T-34C CYP17. The A66G MTRR genotypes showed deviation from Hardy-Weinberg equilibrium (p=0.000), the genotypes are not segregating independently (p=0.036). No association of polymorphisms with clinicopathological features was observed.
Juliana De Oliveira Cruz. 2020. \u201cAssociation of CYP17 and MTRR Gene Polymorphisms with Clinicopathological Features of Breast Cancer Patients\u201d. Global Journal of Medical Research - F: Diseases GJMR-F Volume 20 (GJMR Volume 20 Issue F7): .
Crossref Journal DOI 10.17406/gjmra
Print ISSN 0975-5888
e-ISSN 2249-4618
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Total Score: 107
Country: Brazil
Subject: Global Journal of Medical Research - F: Diseases
Authors: Juliana De Oliveira Cruz, Verena Silva Santos, Jakeline Santos Oliveira, Samuel Dos Santos Oliveira, Claudia Leal Macedo, Sandra Mara Bispo Sousa, Patricia Santos Pereira Lima (PhD/Dr. count: 0)
View Count (all-time): 129
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Publish Date: 2020 07, Fri
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Allele frequencies of T-34C CYP17 and A66G MTRR polymorphisms in breast cancer samples and the correlation with clinicopathological data can contribute to the prognosis and knowledge of the genetic profile of a population. In this study, was analized the association of T-34C CYP17 and A66G MTRR polymorphisms with clinicopathological data in 82 samples of invasive ductal breast carcinoma in the Southwest region of Bahia. PCR-RFLP was used to determine the genotypes for A66G MTRR and T-34C CYP17 polymorphisms. The allele frequency was 0.369 and 0.631 for A66G MTRR; 0.672 and 0.328 for T-34C CYP17. The A66G MTRR genotypes showed deviation from Hardy-Weinberg equilibrium (p=0.000), the genotypes are not segregating independently (p=0.036). No association of polymorphisms with clinicopathological features was observed.
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