Literature DB >> 26909997

Analysis of polymorphisms in codons 11, 72 and 248 of TP53 in Brazilian women with breast cancer.

B C Almeida1, J P F O Kleine1, C M Camargo-Kosugi1,2, M R Lisboa1, C N França3, J P França4, I D C G Silva1.   

Abstract

The association between TP53 gene polymorphisms and breast cancer (BC) in Brazilian women is a controversial topic. In this cross-sectional study, we evaluated the association between clinical pathological variables and three polymorphisms (TP53*11, TP53*72, and TP53*248) in BC patients and controls. Genomic DNA was extracted from the blood cells of 393 participants; the cancer-free control subjects were 26-72 years old (41 ± 11.03) and the BC patients were 28-80 years old (51 ± 10.70). We used standard polymerase chain reaction-restriction fragment length polymorphism and confirmed the results by genetic sequencing. In TP53*11, there was 100% homozygous Glu distribution in both groups. TP53*72 showed genotypic distribution: in the control group, there was 16.10% homozygous Pro, and 42.44% heterozygous and 41.46% homozygous Arg; in the BC group, there was 15.43% homozygous Pro, and 42.55% heterozygous and 42.02% homozygous Arg. The relative frequency of each allele was 0.37% for Pro and 0.63% for Arg in the control group, and 0.37% for Pro and 0.63% for Arg in the BC group. The nuclear grade (P = 0.0084) and adapted histological grade (P = 0.0265) were associated with TP53*72. The distribution of the codon 72 genotypes did not deviate from Hardy-Weinberg equilibrium in either group. In TP53*248, there was 100% homozygous Arg distribution in both groups. In codon 72, the Arg allele is the most prevalent in Brazilian women. TP53*72 may be associated with susceptibility to BC, although more studies are required to evaluate the profile of Brazilian women with BC.

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Year:  2016        PMID: 26909997     DOI: 10.4238/gmr.15017055

Source DB:  PubMed          Journal:  Genet Mol Res        ISSN: 1676-5680


  4 in total

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Authors:  Valentina A Zavala; Silvia J Serrano-Gomez; Julie Dutil; Laura Fejerman
Journal:  Genes (Basel)       Date:  2019-02-18       Impact factor: 4.096

2.  Gene-Environment Interaction between Arg72Pro SNP and Selected Environmental Exposures among Brazilian Women Diagnosed with Benign Breast Disease.

Authors:  Rafaela Soares Senra Da Costa; Rosalina Jorge Koifman; Viviane Ferreira Esteves; Marla Presa Raulino Schilling; Sergio Koifman; Ilce Ferreira Da Silva
Journal:  Asian Pac J Cancer Prev       Date:  2020-12-01

3.  p53 p.Pro72Arg (rs1042522) and Mouse Double Minute 2 (MDM2) Single-Nucleotide Polymorphism (SNP) 309 Variants and Their Interaction in Chronic Lymphocytic Leukemia(CLL): A Survey in CLL Patients from Western Iran.

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Journal:  Int J Hematol Oncol Stem Cell Res       Date:  2021-07-01

Review 4.  Landscape of Germline Mutations in DNA Repair Genes for Breast Cancer in Latin America: Opportunities for PARP-Like Inhibitors and Immunotherapy.

Authors:  Laura Keren Urbina-Jara; Augusto Rojas-Martinez; Emmanuel Martinez-Ledesma; Dione Aguilar; Cynthia Villarreal-Garza; Rocio Ortiz-Lopez
Journal:  Genes (Basel)       Date:  2019-10-10       Impact factor: 4.096

  4 in total

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