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miRNA expression profiles of MDA-MB-231 TNBC cells with defected RARalpha serine-77 phosphorylation

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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE160295
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microRNAs have been shown to be involved in the pathogenesis of TNBC as important regulators of cell proliferation and apoptosis. However, whether the activation of retinoic acid receptor alpha (RARα), a transcription factor, is involved in mediating transcriptional regulation of microRNAs remains elusive. Here, we investigated the differentially expressed miRNAs in triple negative breast cancer cell line MDA-MB-231 overexpressing a phosphorylation-defective mutant RARαS77A, which mimicked activated RARα, in comparison to non-transfected control cells. MDA-MB-231 cells were transfected with lentiviral RARαS77A, a total amount of 3 μg total RNA per sample was used as input material for the small RNA library. Sequencing libraries were generated using NEBNext® Multiplex Small RNA Library Prep Set for Illumina® (NEB, USA.) following the manufacturer’s recommendations and index codes were added to attribute sequences to each sample. Non-transfected cells were used as controls, experiments were performed in triplicates.
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2021-05-05
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