Study of circulating MicroRNA-125b levels in serum exosomes in advanced melanoma

Context: Malignant melanoma is an aggressive tumor that produces exosomes, which contain microRNAs (miRNAs) that could be of utility in following tumoral cell dysregulation. MicroR-125b is a miRNA whose down-regulation seems to be implicated in melanoma progression. Objective: To analyze miR-125b le...

ver descrição completa

Detalhes bibliográficos
Autores: Fernández-de-Sanmamed-Gutiérrez, M. (Miguel)|||/items/35ac602c-f0ff-4664-bbd2-506afc96db09, Rodríguez, C. (Carmen)|||/items/ac57e710-2f7d-40f6-a327-cbdaace019a0, Carranza, O. (Omar)|||/items/6dd07135-53d5-4995-ac8e-9e484da8507d, Martin-Algarra, S. (Salvador)|||/items/2fba8e8b-e087-4ab0-82e3-a4d157f1e0cc, Alegre-Martinez, E. (Estibaliz)|||/items/95dd1405-2d49-46b9-b1de-ebfc074792bf, Gonzalez-Hernandez, Á. (Álvaro)|||/items/901d58bd-7116-4c53-ae90-206bbc0afbd3
Tipo de documento: artigo
Data de publicação:2014
País:España
Recursos:Universidad de Navarra
Repositório:Dadun. Depósito Académico Digital de la Universidad de Navarra
Idioma:inglês
OAI Identifier:oai:dadun.unav.edu:10171/68524
Acesso em linha:https://hdl.handle.net/10171/68524
Access Level:Acceso aberto
Palavra-chave:Malignant melanoma
Exosomes
MicroRNAs (miRNAs)
Tumoral cell dysregulation
Descrição
Resumo:Context: Malignant melanoma is an aggressive tumor that produces exosomes, which contain microRNAs (miRNAs) that could be of utility in following tumoral cell dysregulation. MicroR-125b is a miRNA whose down-regulation seems to be implicated in melanoma progression. Objective: To analyze miR-125b levels in serum, and in exosomes obtained from serum, from patients with advanced melanoma. Design: Serum samples were obtained from 21 patients with advanced melanoma, from 16 disease-free patients with melanoma, and from 19 healthy volunteers. Exosomes were isolated from serum by precipitation, and miR-16 and miR-125b levels were quantified by real-time polymerase chain reaction. Results: MicroR-16, but not miR-125b, was detected in all samples, and miR-16 levels were significantly higher in serum than they were in exosomes. MicroR-16 expression levels did not differ significantly between the 2 groups (patients with melanoma and healthy donors). There was a significant relationship between miR-125b and miR-16 levels in exosomes. Additionally, miR-125b levels in exosomes were significantly lower in patients with melanoma compared with disease-free patients with melanoma and healthy controls. Conclusions: Exosomes can provide a suitable material to measure circulating miRNA in melanoma, and miR-16 can be used as an endogenous normalizer. Lower levels of miR-125b in exosomes obtained from serum are associated with advanced melanoma disease, probably reflecting the tumoral cell dysregulation.