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1.
Ann Oncol ; 24(10): 2571-2575, 2013 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-23852308

RESUMO

BACKGROUND: TNF-α has been proposed as a predictive factor for venous thromboembolism (VTE). Genetic polymorphisms could regulate TNF-α production. However, the relationship between TNFA gene variants and VTE is not clarified. This study aims to investigate the predictive role of five different TNFA gene promoter SNPs, or their haplotype combination(s), for a first VTE episode in gastrointestinal cancer out-patients treated with chemotherapy. PATIENTS AND METHODS: Serum TNF-α levels and TNFA -863C/A, -857C/T, -376G/A, -308G/A and -238G/A gene promoter polymorphisms were retrospectively evaluated in 314 subjects, including 157 controls and 157 Caucasian patients with histologically diagnosed GI cancers beginning chemotherapy delivery (5-fluorouracil either as monotherapy or in combination with platinum compounds or irinotecan). RESULTS: Haplotype analysis showed that a five-loci haplotype (CTGGG haplotype) has higher frequency in GI cancer patients who developed VTE (n = 15) during chemotherapy [odds ratio = 2.7, 95% confidence interval (CI) 1.04-7.11, P = 0.04]. GI patients who remained VTE-free did not differ in CTGGG haplotype frequency from controls. No association was observed between serum TNF-α levels and TNFA haplotype, but both were independent predictors of VTE. Approximately 20% of GI cancer patients carrying the CTGGG haplotype developed VTE compared with 4% of the remaining 101 patients (hazard ratio = 5.6, 95% CI 1.8-17.6, P = 0.003). CONCLUSION: These results suggest that TNFA might represent a candidate gene contributing to VTE pathogenesis in GI cancer patients and suggest that VTE risk during chemotherapy might be genetically identified. Validation studies are needed for translation into clinical practice.


Assuntos
Neoplasias Gastrointestinais/tratamento farmacológico , Fator de Necrose Tumoral alfa/genética , Tromboembolia Venosa/induzido quimicamente , Tromboembolia Venosa/genética , Adulto , Idoso , Idoso de 80 Anos ou mais , Antimetabólitos Antineoplásicos/efeitos adversos , Antimetabólitos Antineoplásicos/uso terapêutico , Antineoplásicos Fitogênicos/efeitos adversos , Antineoplásicos Fitogênicos/uso terapêutico , Camptotecina/efeitos adversos , Camptotecina/análogos & derivados , Camptotecina/uso terapêutico , Estudos de Casos e Controles , Feminino , Fluoruracila/efeitos adversos , Fluoruracila/uso terapêutico , Predisposição Genética para Doença , Haplótipos/genética , Humanos , Irinotecano , Masculino , Pessoa de Meia-Idade , Polimorfismo de Nucleotídeo Único , Regiões Promotoras Genéticas/genética , Estudos Retrospectivos , Risco , Fator de Necrose Tumoral alfa/sangue
3.
Leukemia ; 23(5): 856-62, 2009 May.
Artigo em Inglês | MEDLINE | ID: mdl-19151778

RESUMO

In the acute promyelocytic leukemia (APL) bearing the t(15;17), all-trans-retinoic acid (ATRA) treatment induces granulocytic maturation and complete remission of leukemia. We identified miR-342 as one of the microRNAs (miRNAs) upregulated by ATRA during APL differentiation. This miRNA emerged as a direct transcriptional target of the critical hematopoietic transcription factors PU.1 and interferon regulatory factor (IRF)-1 and IRF-9. IRF-1 maintains miR-342 at low levels, whereas the binding of PU.1 and IRF-9 in the promoter region following retinoic ATRA-mediated differentiation, upregulates miR-342 expression. Moreover, we showed that enforced expression of miR-342 in APL cells stimulated ATRA-induced differentiation. These data identified miR-342 as a new player in the granulocytic differentiation program activated by ATRA in APL.


Assuntos
Diferenciação Celular , Granulócitos/citologia , Fator Regulador 1 de Interferon/genética , Fator Gênico 3 Estimulado por Interferon, Subunidade gama/genética , Leucemia Promielocítica Aguda/genética , MicroRNAs/genética , MicroRNAs/fisiologia , Proteínas Proto-Oncogênicas/genética , Transativadores/genética , Tretinoína/farmacologia , Antineoplásicos/farmacologia , Moléculas de Adesão Celular/genética , Moléculas de Adesão Celular/metabolismo , Imunoprecipitação da Cromatina , Granulócitos/efeitos dos fármacos , Granulócitos/metabolismo , Humanos , Immunoblotting , Imunofenotipagem , Fator Regulador 1 de Interferon/metabolismo , Fator Gênico 3 Estimulado por Interferon, Subunidade gama/metabolismo , Íntrons/genética , Leucemia Promielocítica Aguda/metabolismo , Leucemia Promielocítica Aguda/patologia , Regiões Promotoras Genéticas , Proteínas Proto-Oncogênicas/metabolismo , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Transativadores/metabolismo , Células Tumorais Cultivadas
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