Cargando…

Dysregulated miR-27a-3p promotes nasopharyngeal carcinoma cell proliferation and migration by targeting Mapk10

miRNA-27a-3p is an important regulator of carcinogenesis and other pathological processes. However, its role in laryngeal carcinoma is still unknown. In our previous research, we found that miR-27a-3p expression was upregulated in nasopharyngeal carcinoma (NPC) using a microarray chip. In the presen...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Lihua, Luo, Zhaohui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428281/
https://www.ncbi.nlm.nih.gov/pubmed/28393229
http://dx.doi.org/10.3892/or.2017.5544
Descripción
Sumario:miRNA-27a-3p is an important regulator of carcinogenesis and other pathological processes. However, its role in laryngeal carcinoma is still unknown. In our previous research, we found that miR-27a-3p expression was upregulated in nasopharyngeal carcinoma (NPC) using a microarray chip. In the present study, we identified miR-27a-3p as an endogenous promoter of metastatic invasion. The expression levels of miR-27a-3p were correlated with human metastatic progression outcomes and Kaplan-Meier survival. In silico database analyses revealed that Mapk10 is a potential target of miR-27a-3p, and luciferase reporter assay results revealed that miR-27a-3p directly inhibits the Mapk10 3 untranslated region (3′UTR). Real-time PCR and western blotting results ascertained that Mapk10 expression was regulated by miR-27a-3p. In addition, miR-27a-3p gain-of-function promoted cell proliferation, migration and invasion in 5–8 F NPC cells. These effects partially depended on Mapk10, and loss of miR-27a-3p function had the opposite effects.