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Chinese medical journal · Feb 2021
miRNA-296-5p functions as a potential tumor suppressor in human osteosarcoma by targeting SND1.
- Ya-Zeng Huang, Jun Zhang, Jian-Jian Shen, Ting-Xiao Zhao, and You-Jia Xu.
- Department of Orthopedics, The Second Affiliated Hospital of Soochow University, Soochow, Jiangsu 215004, China.
- Chin. Med. J. 2021 Feb 9; 134 (5): 564-572.
BackgroundThe pathogenesis of osteosarcoma (OS) is still unclear, and it is still necessary to find new targets and drugs for anti-OS. This study aimed to investigate the role and mechanism of the anti-OS effects of miR-296-5p.MethodsWe measured the expression of miR-296-5p in human OS cell lines and tissues. The effect of miR-296-5p and its target gene staphylococcal nuclease and tudor domain containing 1 on proliferation, migration, and invasion of human OS lines was examined. The Student's t test was used for statistical analysis.ResultsWe found that microRNA (miR)-296-5p was significantly downregulated in OS cell lines and tissues (control vs. OS, 1.802 ± 0.313 vs. 0.618 ± 0.235, t = 6.402, P < 0.01). Overexpression of miR-296-5p suppressed proliferation, migration, and invasion of OA cells. SND1 was identified as a target of miR-296-5p by bioinformatic analysis and dual-luciferase reporter assay. Overexpression of SND1 abrogated the effects induced by miR-296-5p upregulation (miRNA-296-5p vs. miRNA-296-5p + SND1, 0.294 ± 0.159 vs. 2.300 ± 0.277, t = 12.68, P = 0.003).ConclusionOur study indicates that miR-296-5p may function as a tumor suppressor by targeting SND1 in OS.Copyright © 2021 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license.
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