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4-(Methylnitrosamino)-1-(3-pyridyl) -1-butanone induces circulating microRNA deregulation in early lung carcinogenesis / 生物医学与环境科学(英文)
Biomedical and Environmental Sciences ; (12): 10-16, 2014.
Artículo en Inglés | WPRIM | ID: wpr-247092
ABSTRACT
<p><b>OBJECTIVE</b>To study the alteration of circulating microRNAs in 4-(methylnitrosamino)-1-(3-pyridyl) -1-butanone (NNK)-induced early stage lung carcinogenesis.</p><p><b>METHODS</b>A lung cancer model of male F344 rats was induced with systemic NNK and levels of 8 lung cancer-associated miRNAs in whole blood and serum of rats were measured by quantitative RT-PCR of each at weeks 1, 5, 10, and 20 following NNK treatment.</p><p><b>RESULTS</b>No lung cancer was detected in control group and NNK treatment group at week 20 following NNK treatment. The levels of some circulating miRNAs were significantly higher in NNK treatment group than in control group. The miR-210 was down-regulated and the miR-206 was up-regulated in NNK treatment group. The expression level of circulating miRNAs changed from week 1 to week 20 following NNK treatment.</p><p><b>CONCLUSION</b>The expression level of circulating miRNAs is related to NNK-induced early stage lung carcinogenesis in rats and can therefore serve as its potential indicator.</p>
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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Patología / Farmacología / Fisiología / Ratas Endogámicas F344 / Sangre / Adenocarcinoma / Regulación de la Expresión Génica / MicroARNs / Línea Celular Tumoral / Carcinogénesis Límite: Animales / Humanos / Masculino Idioma: Inglés Revista: Biomedical and Environmental Sciences Año: 2014 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Patología / Farmacología / Fisiología / Ratas Endogámicas F344 / Sangre / Adenocarcinoma / Regulación de la Expresión Génica / MicroARNs / Línea Celular Tumoral / Carcinogénesis Límite: Animales / Humanos / Masculino Idioma: Inglés Revista: Biomedical and Environmental Sciences Año: 2014 Tipo del documento: Artículo