Department of Orthopaedics, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China; Department of Orthopaedics, West China Hospital Sichuan University, Chengdu, Sichuan, China.
Department of Orthopaedics, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China; Department of Orthopaedics, Zhongda Hospital Southeast University, Nanjing, Jiangsu, China.
Biochem Biophys Res Commun. 2019 Mar 12;510(3):479-486. doi: 10.1016/j.bbrc.2019.01.139. Epub 2019 Feb 5.
Osteosarcoma (OS) has emerged as the most common primary musculoskeletal malignant tumor which affects children and adolescents. A growing number of relevant studies have shown that many microRNAs (miRNAs) play a vital regulatory role in the etiology of various types of cancer. miR-1258 has been widely studied in various cancers, but there have been few studies of its role in OS. In this present study, miR-1258 expression was dramatically decreased in OS tissues as well as OS cell lines. In addition, decreased expression of miR-1258 was significantly associated with malignant clinical manifestations and poor clinical prognosis of patients with OS. Moreover, upregulation of miR-1258 significantly inhibited cell proliferation as well as promoting cell cycle arrest at G0/G1. AKT3 was identified as a direct target of miR-1258 by binding to its 3'-UTR, and miR-1258 was negatively correlated with AKT3 expression in clinical OS tissues. AKT3 was evidently upregulated in OS tissues and cells and upregulation of AKT3 accelerated the progression of OS. Moreover, through a series of rescue experiments, we demonstrated that AKT3 can abolish the role of miR-1258 in suppressing proliferation as well as regulating the cell cycle in OS cells. In conclusion, our results suggest that the miR-1258-AKT3 axis may be a promising prognostic marker and therapeutic target for human OS.
骨肉瘤(OS)已成为影响儿童和青少年的最常见原发性肌肉骨骼恶性肿瘤。越来越多的相关研究表明,许多 microRNAs(miRNAs)在各种类型癌症的发病机制中发挥着重要的调节作用。miR-1258 在各种癌症中都得到了广泛研究,但在 OS 中的作用研究较少。在本研究中,miR-1258 在 OS 组织和 OS 细胞系中的表达显著降低。此外,miR-1258 的表达降低与 OS 患者恶性临床表现和不良临床预后显著相关。此外,miR-1258 的上调显著抑制细胞增殖,并促进细胞周期停滞在 G0/G1 期。AKT3 通过结合其 3'UTR 被鉴定为 miR-1258 的直接靶标,并且 miR-1258 在临床 OS 组织中与 AKT3 表达呈负相关。AKT3 在 OS 组织和细胞中明显上调,上调 AKT3 加速了 OS 的进展。此外,通过一系列的挽救实验,我们证明 AKT3 可以消除 miR-1258 在抑制 OS 细胞增殖和调节细胞周期中的作用。总之,我们的研究结果表明,miR-1258-AKT3 轴可能是人类 OS 的一个有前途的预后标志物和治疗靶点。