Aging · 2019 · 43 citations · 29 references
Life SciencesCell BiologyMolecular BiologyGene ExpressionMolecular OncologyTranscriptomicsCancer TranscriptomicsCellular AgingCellular SenescenceNoncoding Rna BiologyNoncoding Rna In CancerNoncoding Rna TranscriptomicsCellular Senescence ResistanceCircular Rna FunctionCircular RnasNon-coding Rna RegulationNoncoding Rna-mediated EffectsSenescence ModulationSenescence-associated Beta-galactosidaseWhole Transcriptome Analysis
), termed CircCCNB1. Reduced CircCCNB1 expression triggered senescence in young 2BS cells, as measured by increased senescence associated-beta-galactosidase (SA-β-gal) activity, enhanced expression of cyclin-dependent kinase inhibitor 1A (CDKN1A)/P21 and tumor protein 53 (TP53) expression, and reduced cell proliferation. Mechanistically, reduced CircCCNB1 level inhibited cyclin E2 (CCNE2) expression by modulating micro RNA (miR)-449a activity, which repressed cellular proliferation. Our data suggested that CircCCNB1may serve as a sponge against miR-449a to delay cellular senescence by targeting CCNE2. Targeting CircCCNB1 may represent a promising strategy for aging and age-related disease interventions. Furthermore, we also identified and characterized several kinds of the CircCCNB1-binding proteins (CBPs), which may contribute to the degradation of CircCCNB1.
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