
doi: 10.4149/neo_2014_034
pmid: 24824927
Accumulative evidence has confirmed that, miR-17-92, a typical polycistronic mRNA cluster, was up-regulated in various solid tumors, and play an important role in the occurrence and development progress of tumors. In our study, we detected the six members of miR-17-92 cluster in osteosarcoma cell line, finding that the expression of miR-17 and miR-19b was up-regulated significantly. Further studies have found that Mfn1 was one of the target genes of miR-19b and the transcription and expression level of Mfn1 were down-regulated by miR-19b. MTS, flow cytometry, TUNEL-DAPI, Annexin V-FITC and transwell assay demonstrated that Mfn1 significantly blocked the cell cycle, promoted apoptosis and inhibited proliferation and invasion of osteosarcoma cells. Whereas, miR-19b targets 3'UTR sequences of Mfn1 genes inhibit the expression of Mfn1, thus inhibited Mfn1 triggered anti-cancer effect. Taken together, miR-19b functions by targeting Mfn1 reduce the protein expression level, thus provides a novel target to understand the molecular biology and genetics mechanisms of occurrence and development of osteosarcoma, contributing to the diagnosis and therapy of osteosarcoma.
Osteosarcoma, Apoptosis, Bone Neoplasms, Cell Cycle Checkpoints, Mitochondrial Membrane Transport Proteins, GTP Phosphohydrolases, Gene Expression Regulation, Neoplastic, MicroRNAs, Cell Line, Tumor, Humans, Neoplasm Invasiveness, 3' Untranslated Regions
Osteosarcoma, Apoptosis, Bone Neoplasms, Cell Cycle Checkpoints, Mitochondrial Membrane Transport Proteins, GTP Phosphohydrolases, Gene Expression Regulation, Neoplastic, MicroRNAs, Cell Line, Tumor, Humans, Neoplasm Invasiveness, 3' Untranslated Regions
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