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MiR-1281是一种p53反应性微小RNA,通过靶向USP39在内质网应激时损害人骨肉瘤细胞的存活。

MiR-1281, a p53-responsive microRNA, impairs the survival of human osteosarcoma cells upon ER stress via targeting USP39.

作者信息

Jiang Jian, Ma Binbin, Li Xiaojie, Jin Wenlong, Han Chuanchun, Wang Ling, Wang Hong

机构信息

Department of Spine Surgery, First Affiliated Hospital, Institute of Cancer Stem Cell of Dalian Medical University Dalian 116011, China.

Department of Neurosurgery, Second Affiliated Hospital of Dalian Medical University Dalian 116027, China.

出版信息

Am J Cancer Res. 2018 Sep 1;8(9):1764-1774. eCollection 2018.

Abstract

MicroRNAs (miRNAs) are small regulatory non-coding RNAs that have been reported to play an important role in a variety of cellular functions. Recent studies indicated that some miRNAs are involved in regulating endoplasmic reticulum (ER) stress adaptation. However, the miRNAs were still unknown in osteosarcoma. In this study, we demonstrated that miR-1281 induced by ER stress promoted cell apoptosis and decreased ER stress adaptation of osteosarcoma and . Further mechanistic studies revealed that p53, an important tumor suppressor, directly bound to the promoter of miR-1281, leading to its increase under ER stress. Additionally, our data suggest that USP39 was the target of miR-1281 and participated in ER stress-induced cell apoptosis. Thus, our findings suggest a new role for miR-1281 in osteosarcoma and suggest that the p53-dependent, miR-1281-mediated USP39 pathway inhibits the survival of human osteosarcoma cells under ER stress.

摘要

微小RNA(miRNA)是一类小的调节性非编码RNA,据报道其在多种细胞功能中发挥重要作用。最近的研究表明,一些miRNA参与调节内质网(ER)应激适应。然而,骨肉瘤中这些miRNA仍不清楚。在本研究中,我们证明内质网应激诱导的miR-1281促进骨肉瘤细胞凋亡并降低内质网应激适应能力。进一步的机制研究表明,重要的肿瘤抑制因子p53直接结合到miR-1281的启动子上,导致其在内质网应激下表达增加。此外,我们的数据表明USP39是miR-1281的靶标,并参与内质网应激诱导的细胞凋亡。因此,我们的研究结果表明miR-1281在骨肉瘤中具有新的作用,并表明p53依赖性、miR-1281介导的USP39途径在内质网应激下抑制人骨肉瘤细胞的存活。

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