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Dysregulated miR-671-5p / CDR1-AS / CDR1 / VSNL1 axis is involved in glioblastoma multiforme

MiR-671-5p is encoded by a gene localized at 7q36.1, a region amplified in human glioblastoma multiforme (GBM), the most malignant brain cancer. To investigate whether expression of miR-671-5p were altered in GBM, we analyzed biopsies from a cohort of forty-five GBM patients and from five GBM cell l...

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Detalles Bibliográficos
Autores principales: Barbagallo, Davide, Condorelli, Angelo, Ragusa, Marco, Salito, Loredana, Sammito, Mariangela, Banelli, Barbara, Caltabiano, Rosario, Barbagallo, Giuseppe, Zappalà, Agata, Battaglia, Rosalia, Cirnigliaro, Matilde, Lanzafame, Salvatore, Vasquez, Enrico, Parenti, Rosalba, Cicirata, Federico, Di Pietro, Cinzia, Romani, Massimo, Purrello, Michele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4826240/
https://www.ncbi.nlm.nih.gov/pubmed/26683098
http://dx.doi.org/10.18632/oncotarget.6621
Descripción
Sumario:MiR-671-5p is encoded by a gene localized at 7q36.1, a region amplified in human glioblastoma multiforme (GBM), the most malignant brain cancer. To investigate whether expression of miR-671-5p were altered in GBM, we analyzed biopsies from a cohort of forty-five GBM patients and from five GBM cell lines. Our data show significant overexpression of miR-671-5p in both biopsies and cell lines. By exploiting specific miRNA mimics and inhibitors, we demonstrated that miR-671-5p overexpression significantly increases migration and to a less extent proliferation rates of GBM cells. Through a combined in silico and in vitro approach, we identified CDR1-AS, CDR1, VSNL1 as downstream miR-671-5p targets in GBM. Expression of these genes significantly decreased both in GBM biopsies and cell lines and negatively correlated with that of miR-671-5p. Based on our data, we propose that the axis miR-671-5p / CDR1-AS / CDR1 / VSNL1 is functionally altered in GBM cells and is involved in the modification of their biopathological profile.