Suppr超能文献

去甲基化介导的miR-129-5p上调通过靶向人含缬酪肽蛋白(VCP)抑制成骨性骨肉瘤的恶性表型。

Demethylation-mediated miR-129-5p up-regulation inhibits malignant phenotype of osteogenic osteosarcoma by targeting Homo sapiens valosin-containing protein (VCP).

作者信息

Long Xin Hua, Zhou Yun Fei, Peng Ai Fen, Zhang Zhi Hong, Chen Xuan Yin, Chen Wen Zhao, Liu Jia Ming, Huang Shan Hu, Liu Zhi Li

机构信息

Department of Orthopedics, The First Affiliated Hospital of Nanchang University, Yong Wai Zheng Street 17, Nanchang, Jiangxi, 330006, People's Republic of China.

出版信息

Tumour Biol. 2015 May;36(5):3799-806. doi: 10.1007/s13277-014-3021-7. Epub 2015 Jan 8.

Abstract

Previous studies demonstrated that increased Homo sapiens valosin-containing protein (VCP) may be involved in osteosarcoma (OS) metastasis. However, the underlying mechanism of VCP over-expression in OS remains unknown. In the present study, we found a significantly negative correlation between miR-129-5p and VCP protein expression in OS tissues with pulmonary metastasis (Spearman's rho, rs = -0.948). Bioinformatical prediction, Luciferase reporter assay, Western blot, and RT-PCR assays performed on OS cells indicated that VCP is a target of miR-129-5p. In addition, three CPG islands in the region of miR-129-5p promoter were detected by bioinformatical prediction, and significantly higher expression of miR-129-5p and lower methylation level of miR-129-2 gene in OS cells treated with 5-Aza-2'-deoxycytidine (a potent DNA demethylating agent) than in those untreated cells were observed. Furthermore, lower migratory and invasive ability was found in cells with elevated miR-129-5p than in those with decreased miR-129-5p. These findings indicated that increased miR-129-5p may be mediated by demethylation and inhibit OS cell migration and invasion by targeting VCP in OS, and targeting miR-129-5p/VCP signaling pathway may serve as a therapeutic strategy for OS management, although further studies will be necessary.

摘要

先前的研究表明,人类含缬酪肽蛋白(VCP)水平升高可能与骨肉瘤(OS)转移有关。然而,OS中VCP过表达的潜在机制仍不清楚。在本研究中,我们发现肺转移OS组织中miR-129-5p与VCP蛋白表达之间存在显著负相关(Spearman秩相关系数,rs = -0.948)。对OS细胞进行的生物信息学预测、荧光素酶报告基因检测、蛋白质免疫印迹和逆转录-聚合酶链反应检测表明,VCP是miR-129-5p的靶标。此外,通过生物信息学预测在miR-129-5p启动子区域检测到三个CPG岛,并且观察到用5-氮杂-2'-脱氧胞苷(一种有效的DNA去甲基化剂)处理的OS细胞中miR-129-5p的表达显著高于未处理细胞,而miR-129-2基因的甲基化水平则较低。此外,与miR-129-5p降低的细胞相比,miR-129-5p升高的细胞迁移和侵袭能力更低。这些发现表明,miR-129-5p增加可能由去甲基化介导,并通过靶向OS中的VCP抑制OS细胞迁移和侵袭,尽管还需要进一步研究,但靶向miR-129-5p/VCP信号通路可能作为OS治疗的一种策略。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验