Cancer Biology & Therapy · 2021 · 32 citations · 18 references
MedicineMolecular BiologyOncologyGene ExpressionMolecular OncologyTranscriptional RegulationBreast Cancer RadiobiologyCancer Cell SignalingNoncoding Rna BiologyNoncoding Rna FunctionNoncoding Rna In CancerRna StabilityCytoplasmic PolyadenylationLong Non-coding Ribonucleic AcidsLong Non-coding Rna FunctionLong Noncoding Rna RegulationLong Noncoding Rna-mediated ResistanceLuciferase Reporter AssaysNoncoding Rna-mediated Gene RegulationRna Immunoprecipitation
assays, it was confirmed that the knockdown of LINC00504 could enhance the radio-sensitivity of BC cells. The regulatory mechanism of LINC00504 in BC was also verified by chromatin immunoprecipitation (ChIP), RNA immunoprecipitation (RIP) and luciferase reporter assays. From the experimental results, we knew that the up-regulation of LINC00504 was mediated by signal transducer and activator of transcription 1 (STAT1). Moreover, LINC00504 stabilized the expression of cytoplasmic polyadenylation element-binding protein 2 (CPEB2) via binding to TATA-box binding protein associated factor 15 (TAF15). Furthermore, rescue assays validated that LINC00504 participated in regulating the radio-sensitivity of BC cells via up-regulating CPEB2. In summary, our study disclosed that STAT1 could mediate LINC00504 and weaken the radio-sensitivity of BC cells via binding to TAF15 and stabilizing CPEB2 expression.
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Breast cancer: basics, screening, diagnostics and treatment.
Bernhard Wörmann · PubMed · 2017 · 104 citations