Suppr超能文献

miR-1258 的过表达通过靶向 AKT3 抑制骨肉瘤细胞增殖。

Overexpression of miR-1258 inhibits cell proliferation by targeting AKT3 in osteosarcoma.

机构信息

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.

出版信息

Biochem Biophys Res Commun. 2019 Mar 12;510(3):479-486. doi: 10.1016/j.bbrc.2019.01.139. Epub 2019 Feb 5.

Abstract

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.

摘要

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验