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Blood Cells Mol Dis ; 57: 54-7, 2016 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-26852656

RESUMO

The classical chromosome Philadelphia-negative myeloproliferative neoplasms (MPNs) are a group of disorders that share clinical, hematological, and histological features. Proinflammatory cytokines such as tumor necrosis factor-α (TNF-α) are elevated in patients with MPN. The aim of this study was to verify the association between the polymorphisms of TNF gene (-308G/A and -238 G/A) in BCR-ABL-negative MPN in our population. Blood samples obtained from MPN patients were genotyped for the JAK2V617F mutation and both TNF polymorphisms using PCR-RFLP. Thirty three (26.8%) patients with polycythemia vera (PV), 35 (28.7%) essential thrombocythemia (ET), 22 (17.7%) primary myelofibrosis (PMF), and 33 (26.8%) with unclassifiable MPN (MPNu) were included in the study. The JAK2 V617F mutation was detected in 94 (76.42%) patients. Were observed a significant increase on the frequency of the TNF-238 GA genotype in MPN patients compared to controls (OR=2.21, 95% CI=1.02-4.80, P<0.04). The distribution of the genotypes and allelic frequencies of TNF-308 was significantly different among the MPNs, JAK2V617F positive, PV and PMF, and controls. Our data has demonstrated that the polymorphisms on TNF-238 GA, TNF-308 GA were associated to MPN development in this population, triggered by JAK2 V617F mutation.


Assuntos
Janus Quinase 2/genética , Leucemia Mieloide Crônica Atípica BCR-ABL Negativa/genética , Policitemia Vera/genética , Polimorfismo Genético , Mielofibrose Primária/genética , Trombocitemia Essencial/genética , Fator de Necrose Tumoral alfa/genética , Adulto , Idoso , Alelos , Brasil , Estudos de Casos e Controles , Análise Mutacional de DNA , Feminino , Expressão Gênica , Predisposição Genética para Doença , Humanos , Leucemia Mieloide Crônica Atípica BCR-ABL Negativa/diagnóstico , Leucemia Mieloide Crônica Atípica BCR-ABL Negativa/patologia , Masculino , Pessoa de Meia-Idade , Policitemia Vera/diagnóstico , Policitemia Vera/patologia , Mielofibrose Primária/diagnóstico , Mielofibrose Primária/patologia , Regiões Promotoras Genéticas , Trombocitemia Essencial/diagnóstico , Trombocitemia Essencial/patologia
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