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miR-98 suppresses melanoma metastasis through a negative feedback loop with its target gene IL-6
Experimental & Molecular Medicine ; : e116-2014.
Article Dans Anglais | WPRIM | ID: wpr-222036
ABSTRACT
Dysregulated microRNA (miRNA) expression has a critical role in tumor development and metastasis. However, the mechanism by which miRNAs control melanoma metastasis is unknown. Here, we report reduced miR-98 expression in melanoma tissues with increasing tumor stage as well as metastasis; its expression is also negatively associated with melanoma patient survival. Furthermore, we demonstrate that miR-98 inhibits melanoma cell migration in vitro as well as metastatic tumor size in vivo. We also found that IL-6 is a target gene of miR-98, and IL-6 represses miR-98 levels via the Stat3-NF-kappaB-lin28B pathway. In an in vivo melanoma model, we demonstrate that miR-98 reduces melanoma metastasis and increases survival in part by reducing IL-6 levels; it also decreases Stat3 and p65 phosphorylation as well as lin28B mRNA levels. These results suggest that miR-98 inhibits melanoma metastasis in part through a novel miR-98-IL-6-negative feedback loop.
Sujets)
Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Transduction du signal / Régulation négative / Régulation de l'expression des gènes tumoraux / Analyse de survie / Interleukine-6 / MicroARN / Lignée cellulaire tumorale / Mélanome / Souris de lignée C57BL / Métastase tumorale Type d'étude: Étude pronostique Limites du sujet: Animaux / Humains / Mâle langue: Anglais Texte intégral: Experimental & Molecular Medicine Année: 2014 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Transduction du signal / Régulation négative / Régulation de l'expression des gènes tumoraux / Analyse de survie / Interleukine-6 / MicroARN / Lignée cellulaire tumorale / Mélanome / Souris de lignée C57BL / Métastase tumorale Type d'étude: Étude pronostique Limites du sujet: Animaux / Humains / Mâle langue: Anglais Texte intégral: Experimental & Molecular Medicine Année: 2014 Type: Article