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pmid:31829261
miR-624-5p promoted tumorigenesis and metastasis by suppressing hippo signaling through targeting PTPRB in osteosarcoma cells.
Yongjun Luo · Wei Liu · Pengyu Tang · Dongdong Jiang · Changjiang Gu · Yumin Huang · Fangyi Gong · Yuluo Rong · Dingfei Qian · Jian Chen · Zheng Zhou · Shujie Zhao · Jiaxing Wang · Tao Xu · Yongzhong Wei · Guoyong Yin · Jin Fan · Weihua Cai
Journal of experimental & clinical cancer research : CR · 2019 doi:10.1186/s13046-019-1491-6
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Complete file
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This study aimed to elucidate the association between miR-624-5p expression and osteosarcoma (OS) development and to investigate its underlying mechanism.\nMETHODS: We analyzed GSE65071 from the GEO database and found miR-624-5p was the most upregulated miRNA. The expression of miR-624-5p and its specific target gene were determined in human OS specimens and cell lines by RT-PCR and western blot. The effects of miR-624-5p depletion or ectopic expression on OS proliferation, migration and invasion were evaluated in vitro using CCK-8 proliferation assay, colony formation assay, transwell assay, would-healing assay and 3D spheroid BME cell invasion assay respectively. We investigated in vivo effects of miR-624-5p using a mouse tumorigenicity model. Besides, luciferase reporter assays were employed to identify interactions between miR-624-5p and its specific target gene.\nRESULTS: miR-624-5p expression was upregulated in OS cells and tissues, and overexpressing miR-624-5p led to a higher malignant level of OS, including cell proliferation, migration and invasion in vitro and in vivo. Protein tyrosine phosphatase receptor type B (PTPRB) was negatively correlated with miR-624-5p expression in OS tissues. Using the luciferase reporter assay and Western blotting, PTPRB was confirmed as a downstream target of miR-624-5p. PTPRB restored the effects of miR-624-5p on OS migration and invasion. The Hippo signaling pathway was identified as being involved in the miR-624-5p/PTPRB axis.\nCONCLUSIONS: In conclusion, our results suggest that miR-624-5p is a negative regulator of PTPRB and a risk factor for tumor metastasis in OS progression.", "claims": [{"id": "claim-method", "statement": "The χ2 test was used to analyze the association of miR-624-5p expression level with clinicopathological features. Independent t-tests were used to compare differences between the two groups. A paired t-test was used to analyze miR-624-5p and PTPRB mRNA levels in tissue samples. One-way or two-way ANOVA with Bonferroni post hoc test was used for multivariate analysis. 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