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A-to-I miR-378a-3p editing can prevent melanoma progression via regulation of PARVA expression

Previously we have reported that metastatic melanoma cell lines and tumor specimens have reduced expression of ADAR1 and consequently are impaired in their ability to perform A-to-I microRNA (miRNA) editing. The effects of A-to-I miRNAs editing on melanoma growth and metastasis are yet to be determi...

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Detalles Bibliográficos
Autores principales: Velazquez-Torres, Guermarie, Shoshan, Einav, Ivan, Cristina, Huang, Li, Fuentes-Mattei, Enrique, Paret, Harrison, Kim, Sun Jin, Rodriguez-Aguayo, Cristian, Xie, Victoria, Brooks, Denise, Jones, Steven J. M., Robertson, A. Gordon, Calin, George, Lopez-Berenstein, Gabriel, Sood, Anil, Bar-Eli, Menashe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5792646/
https://www.ncbi.nlm.nih.gov/pubmed/29386624
http://dx.doi.org/10.1038/s41467-018-02851-7
Descripción
Sumario:Previously we have reported that metastatic melanoma cell lines and tumor specimens have reduced expression of ADAR1 and consequently are impaired in their ability to perform A-to-I microRNA (miRNA) editing. The effects of A-to-I miRNAs editing on melanoma growth and metastasis are yet to be determined. Here we report that miR-378a–3p is undergoing A-to-I editing only in the non-metastatic but not in metastatic melanoma cells. The function of the edited form is different from its wild-type counterpart. The edited form of miR-378a-3p preferentially binds to the 3′-UTR of the PARVA oncogene and inhibits its expression, thus preventing the progression of melanoma towards the malignant phenotype. Indeed, edited miR-378a-3p but not its WT form inhibits melanoma metastasis in vivo. These results further emphasize the role of RNA editing in melanoma progression.