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Braz J Med Biol Res ; 51(3): e6426, 2018 Jan 11.
Artículo en Inglés | MEDLINE | ID: mdl-29340520

RESUMEN

Occupational noise-induced hearing loss (ONIHL) is a prevalent occupational disorder that impairs auditory function in workers exposed to prolonged noise. However, serum microRNA expression in ONIHL subjects has not yet been studied. We aimed to compare the serum microRNA expression profiles in male workers of ONIHL subjects and controls. MicroRNA microarray analysis revealed that four serum microRNAs were differentially expressed between controls (n=3) and ONIHL subjects (n=3). Among these microRNAs, three were upregulated (hsa-miR-3162-5p, hsa-miR-4484, hsa-miR-1229-5p) and one was downregulated (hsa-miR-4652-3p) in the ONIHL group (fold change >1.5 and Pbon value <0.05). Real time quantitative PCR was conducted for validation of the microRNA expression. Significantly increased serum levels of miR-1229-5p were found in ONIHL subjects compared to controls (n=10 for each group; P<0.05). A total of 659 (27.0%) genes were predicted as the target genes of miR-1229-5p. These genes were involved in various pathways, such as mitogen-activated protein kinase (MAPK) signaling pathway. Overexpression of miR-1229-5p dramatically inhibited the luciferase activity of 3' UTR segment of MAPK1 (P<0.01). Compared to the negative control, HEK293T cells expressing miR-1229-5p mimics showed a significant decline in mRNA levels of MAPK1 (P<0.05). This preliminary study indicated that serum miR-1229-5p was significantly elevated in ONIHL subjects. Increased miR-1229-5p may participate in the pathogenesis of ONIHL through repressing MAPK1 signaling.


Asunto(s)
Pérdida Auditiva Provocada por Ruido/sangre , MicroARNs/sangre , Proteína Quinasa 1 Activada por Mitógenos/análisis , Enfermedades Profesionales/sangre , Exposición Profesional/efectos adversos , Adulto , Biomarcadores/sangre , Estudios de Casos y Controles , Regulación de la Expresión Génica , Ontología de Genes , Pérdida Auditiva Provocada por Ruido/genética , Humanos , Masculino , MicroARNs/genética , Persona de Mediana Edad , Enfermedades Profesionales/genética , Reacción en Cadena en Tiempo Real de la Polimerasa
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