Cancer Management and Research · 2019 · 26 citations · 17 references
MedicineCancer BiologyMolecular BiologyGene ExpressionMolecular OncologyOncogenesCancer GenomicsCancer ProgressionNoncoding Rna FunctionNoncoding Rna In CancerTumor Suppressor GenesBreast Cancer ProgressionCancer-related Noncoding Rna FunctionLong Non-coding Rna FunctionLong Noncoding Rna RegulationMicrorna Function In CancerMicrorna-mediated OncogenesisNoncoding Rna Expression ProfilingOncogene Expression Analysis
Purpose: Long intergenic noncoding RNA 01121 ( LINC01121 ) has been reported to be aberrantly expressed and acts as an oncogene in pancreatic cancer. However, the detailed molecular mechanism of LINC01121 in breast cancer remains largely unclear. In this study, we aimed to investigate the expression and biological function of LINC01121 in breast cancer. Methods: LINC01121 and miR-150-5p expression were measured in breast cancer cell lines using quantitative reverse transcription PCR. MTS and flow cytometry assays were performed to determine cell proliferation, the cell cycle, and apoptosis. Cell migration and invasion were assessed by transwell assay. The protein expression of HMGA2 in breast cancer cell lines was measured by Western blotting. A luciferase reporter assay was used to assess the binding of LINC01121 and miR-150-5p . Results: We found that LINC01121 was markedly up-regulated in breast cancer cell lines compared with normal breast epithelial cells. LINC01121 down-regulation markedly suppressed cell proliferation, cell cycle progression, migration, and invasion and promoted apoptosis in breast cancer cells. Further investigation showed that LINC01121 could serve as a molecular sponge for miR-150-5p and indirectly modulate the expression of its target, HMGA2. Moreover, miR-150-5p knockdown rescued the effects of LINC01121 down-regulation on HMGA2 protein expression, cell proliferation, cell cycle progression, apoptosis, migration, and invasion in breast cancer cells. Conclusion: Knockdown LINC01121 inhibited breast cancer cell proliferation, migration, and invasion via the miR-150-5p /HMGA2 axis. Keywords: breast cancer, LINC01121 , growth, migration, invasion, miR-150-5p Corrigendum for this paper has been published
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