Journal of Cellular Biochemistry · 2019 · 49 citations · 30 references
MedicineCancer BiologyOncologyGene ExpressionMolecular OncologyTumor ProgressionCancer ProgressionCancer TranscriptomicsCell Cycle SignalingNoncoding Rna BiologyNoncoding Rna FunctionNoncoding Rna In CancerCancer BioinformaticsCell Cycle DynamicsCell Cycle InhibitionGlioblastoma Molecular PathwaysGlioblastoma Tumor BiologyLong Noncoding Rna RegulationNoncoding Rna Expression ProfilingNoncoding Rna-mediated Gene Regulation
Long noncoding RNAs (lncRNAs) are vital mediators involved in cancer progression. Previous studies confirmed that FOXD2 adjacent opposite strand RNA 1 (FOXD2-AS1) is upregulated in tumor diseases. The potential influence of FOXD2-AS1 in glioma progression, however, remains unknown. In this paper, FOXD2-AS1 was found to be upregulated in glioma tissues. Its level was linked with glioma stage. Moreover, glioma patients expressing high level of FOXD2-AS1 suffered worse prognosis. Biological functions of FOXD2-AS1 in glioma cells were analyzed through integrative bioinformatics and TCGA RNA sequencing data analysis. Pathway enrichment analysis uncovered that FOXD2-AS1 was mainly linked with cell cycle regulation in both low-grade glioma and glioblastoma. Further experiments demonstrated that silence of FOXD2-AS1 inhibited proliferation, arrested cell cycle and downregulated cyclin-dependent kinase 1 (CDK1) in human glioma cells. Dual-luciferase reporter assay confirmed that FOXD2-AS1 upregulated CDK1 by sponging miR-31. Rescue assays were performed and confirmed the regulatory loop FOXD2-AS1/miR-31/CDK1 in glioma. Collectively, our results indicated that the FOXD2-AS1/miR-31/CDK1 axis influenced glioma progression, providing a potential new target for glioma patients.
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