MicroRNA‑466 inhibits osteosarcoma cell proliferation and induces apoptosis by targeting CCND1

癌基因 癌症研究 小RNA 细胞周期 细胞凋亡 骨肉瘤 细胞周期蛋白D1 细胞生长 生物 分子医学 癌症 细胞 基因 遗传学 生物化学
作者
Wei Cao,Le Fang,Siyong Teng,Hongwei Chen,Tiejun Liu
出处
期刊:Experimental and Therapeutic Medicine [Spandidos Publications]
被引量:10
标识
DOI:10.3892/etm.2018.6888
摘要

Emerging pieces of evidence indicate that microRNA-466 (miR-466) serves as a tumor suppressor in several human tumors, including colorectal cancer and prostate cancer. However, whether miR-466 is involved in osteosarcoma (OS) progression remains largely unknown. The present study demonstrated that miR-466 was significantly downregulated in OS tissues and cell lines. Furthermore, it was revealed that the expression of miR-466 was negatively correlated with OS severity. Moreover, low miR-466 expression in patients with OS predicted poor prognosis. Through functional experiments, miR-466 overexpression significantly inhibited the proliferation and cell cycle of OS cells while inducing cellular apoptosis. In terms of mechanism, it was revealed that CCND1 was a target of miR-466 in OS cells. miR-466 overexpression suppressed CCND1 expression in OS cells. A reverse association was observed between the expression levels of miR-466 and CCND1 in OS tissues. Furthermore, CCND1 restoration in OS cells significantly rescued the effects of miR-466 on cellular proliferation and apoptosis. Overall, the results of the present study demonstrated that miR-466 suppressed OS progression by targeting CCND1, suggesting that miR-466 may be a promising biomarker and therapeutic target for OS prognosis and treatment.

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