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1.
Mol Biol Rep ; 40(8): 4883-7, 2013 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-23649769

RESUMO

The close relationship between aflatoxins and 249ser TP53 gene mutation (AGG to AGT, Arg to Ser) in hepatocellular carcinoma (HCC) makes this mutation an indirect indicator of dietary contamination with this toxin. We have examined the prevalence of codon 249 TP53 mutation in 41 HCC and 74 liver cirrhosis (without HCC) cases diagnosed at the HUCAM University Hospital in Vitoria, Espírito Santo State, Brazil. DNA was extracted from paraffin sections and from plasma. The mutation was detected by DNA amplification, followed by restriction endonuclease digestion and confirmed by direct sequencing. DNA restriction showed 249ser mutation in 16 HCC and 13 liver cirrhosis, but sequencing confirmed mutations in only 6 HCC and 1 liver cirrhosis. In addition, sequencing revealed 4 patients with mutations at codon 250 (250ser and 250leu) in HCC cases. The prevalence of TP53 mutation was 10/41 (24.3%) in HCC and 1/74 (1.4%) in liver cirrhosis. No relationship between the presence of mutations and the etiology of HCC was observed. TP53 exon 7 mutations, which are related to aflatoxins exposure, were found at 14.6% (249ser), 7.3% (250leu) and 2.4% (250ser) in 41 cases of HCC and 1.4% in 74 liver cirrhosis (without HCC) cases, suggesting a moderate dietary exposure to aflatoxins in the Espírito Santo State, Brazil.


Assuntos
Aflatoxinas/toxicidade , Carcinoma Hepatocelular/genética , Cirrose Hepática/genética , Neoplasias Hepáticas/genética , Proteína Supressora de Tumor p53/genética , Sequência de Bases , Brasil , Primers do DNA/genética , Contaminação de Alimentos , Humanos , Dados de Sequência Molecular , Mutação de Sentido Incorreto/genética , Polimorfismo de Fragmento de Restrição , Análise de Sequência de DNA
2.
J Neurol Sci ; 269(1-2): 113-7, 2008 Jun 15.
Artigo em Inglês | MEDLINE | ID: mdl-18262566

RESUMO

There is a current lack of molecular studies analyzing the behavior of trinucleotide repeat expansions causative of Late Onset Spinocerebellar Ataxias in the Brazilian population. Therefore, this manuscript analyses normal families, as well as one hundred normal individuals of the Espirito Santo State to determine the trinucleotide repeat behavior and the allelic frequencies found in this population. The analysis of normal families demonstrated that, instead of being always stably transmitted over generations, expansions can occur between two generations of unaffected individuals, possibly contributing for the appearance of the ataxic phenotype. Allelic frequency studies demonstrated that some alleles are prevalent in the population, namely, allele 32 for the ATXN1 locus (21.5%); allele 21 for the ATXN2 locus (50%); allele 21 and 23 for the ATXN3 locus (14% each); allele 12 for the ATXN6 locus (21%) and allele 10 for the ATXN7 locus (22.5%).


Assuntos
Saúde da Família , Ataxias Espinocerebelares/genética , Expansão das Repetições de Trinucleotídeos/genética , Idade de Início , Brasil/epidemiologia , Análise Mutacional de DNA , Feminino , Frequência do Gene , Genótipo , Humanos , Masculino , Ataxias Espinocerebelares/epidemiologia
3.
Forensic Sci Int Genet ; 3(2): 125-7, 2009 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-19215882

RESUMO

DNA isolation is the initial step of most genetic studies, and ideally it should use a reliable and non-invasive method. Buccal samples are adequate for such purposes, being painless, easy to collect and a very reliable DNA source. FTA Elute Cards are relatively new on the market and are designed for rapid blood DNA extraction, in which DNA is solubilized in water, instead of attached to the paper matrix. In this study, we sought to test if FTA Elute Cards are suitable for buccal DNA extraction. Furthermore, several time and temperature conditions were analyzed in order to determine the best concentration/time ratio. Twenty-five different conditions were tested in quadruplicate and extracted DNA was quantified by real-time PCR.


Assuntos
DNA/isolamento & purificação , Mucosa Bucal/citologia , Papel , Manejo de Espécimes , DNA/análise , DNA/genética , Impressões Digitais de DNA/métodos , Humanos , Reação em Cadeia da Polimerase , Kit de Reagentes para Diagnóstico , Manejo de Espécimes/métodos , Fatores de Tempo
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