Nature Communications · 2018 · 86 citations · 22 references
Life SciencesMolecular BiologyOncologyMetastasisMolecular OncologyTumor ProgressionMicrorna BiogenesisMicrorna BiologyNoncoding Rna In CancerRna EditingRna Editing RegulationRna ModificationCancer Gene EditingEditing Regulation In Noncoding RnasMalignant ProgressionMelanoma ProgressionMicrorna EditingMicrorna Function In CancerMicrorna In CancerMicrorna Regulation In Cancer
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.
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Rebecca L. Siegel, Kimberly D. Miller, Ahmedin Jemal · CA A Cancer Journal for Clinicians · 2017 · 15K citations · Full text