RETRACTED: MiR-129-5p Inhibits Proliferation and Invasion of Chondrosarcoma Cells by Regulating SOX4/Wnt/β-Catenin Signaling Pathway (Retracted article. See vol. 57, pg. 50, 2023)

被引:53
|
作者
Zhang, Peng [1 ]
Li, Jifeng [1 ]
Song, Yuze [1 ]
Wang, Xiao [1 ]
机构
[1] Henan Univ, Huaihe Hosp, Dept Osteol, Kaifeng 475000, Henan, Peoples R China
关键词
Chondrosarcoma; miR-129-5p; SOX4; Wnt/beta-catenin signaling pathway; WNT/BETA-CATENIN PATHWAY; UP-REGULATION; DOWN-REGULATION; BETA-CATENIN; SOX4; EXPRESSION; CARCINOMA; MIGRATION; OSTEOSARCOMA; ASSOCIATION;
D O I
10.1159/000477323
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background/Aims: Recently, microRNAs (miRNA) have been identified as novel regulators in Chondrosarcoma (CHS). This study was aimed to identify the roles of miR-129-5p-5p in regulation of SOX4 and Wnt/beta-catenin signaling pathway, as well as cell proliferation and apoptosis in chondrosarcomas. Materials and Methods: Tissue samples were obtained from chondrosarcoma patients. Immunohistochemistry, real-time quantitative RT-PCR (RT-qPCR) and western blot analysis were performed to detect the expressions of miR-129-5p and SOX4. Luciferase assay was conducted to confirm that miR-129-5p directly targeted SOX4 mRNA. Manipulations of miR-129-5p and SOX4 expression were achieved through cell transfection. Cell proliferation, migration and apoptosis were evaluated by CCK-8 assay, colony forming assay, wound healing assay and flow cytometry in vitro. For in vivo experiment, the tumor xenograft model was established to evaluate the effects of miR-129-5p and SOX4 on chondrosarcomas. Results: The expression of miR-129-5p was significantly down-regulated in chondrosarcoma tissues as well as cells in comparison with normal ones, while SOX4 was overactivated. Further studies suggested that miR-129-5p suppressed cell proliferation, migration and promoted apoptosis by inhibiting SOX4 and Wnt/beta-catenin pathway. Conclusion: MiR129-5p inhibits the Wnt/beta-catenin signaling pathway by targeting SOX4 and further suppresses cell proliferation, migration and promotes apoptosis in chondrosarcomas.
引用
收藏
页码:242 / 253
页数:12
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