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微小RNA-1297(HMGA1的一种新型调节因子)参与体内外胶质瘤细胞生长的调控

Involvement of microRNA-1297, a new regulator of HMGA1, in the regulation of glioma cell growth in vivo and in vitro.

作者信息

Wang Jiachong, Xu Xiaoyun, Mo Shaowei, Tian Ye, Wu Jian, Zhang Jianning, Zhao Jiannong

机构信息

Tianjin Neurological Institute, Department of Neurosurgery, General Hospital, Tianjin Medical UniversityTianjin 300052, China; Department of Neurosurgery, The People's Hospital of Hainan ProvinceHaikou 570311, Hainan, China.

Department of Neurosurgery, The People's Hospital of Hainan Province Haikou 570311, Hainan, China.

出版信息

Am J Transl Res. 2016 May 15;8(5):2149-58. eCollection 2016.

Abstract

MicroRNAs (miRNAs) are a class of versatile gene expression regulators, participating in the regulation of gene expression at the post-transcriptional level in both physiological and pathological conditions. Gliomas are the most common brain malignancy in adults, and deregulation of microRNAs takes part in the gliomagenesis process. Here, we found that the expression of miR-1297 is significantly reduced in both glioma cell lines and clinical glioma tissues. Using the MTT assay, soft agar colony formation assay and xenograft tumor formation assay, we show that miR-1297 is a tumor suppressor microRNA in gliomas. We demonstrate that the high mobility group protein A1 (HMGA1) is the functional target of miR-1297 in glioma cells. HMGA1 significantly promotes the growth of glioma cells both in vitro and in vivo. Together, we unveil a new molecular mechanism in gliomas that may shed new light on understanding this brain malignancy.

摘要

微小RNA(miRNA)是一类多功能的基因表达调节因子,在生理和病理条件下均参与转录后水平的基因表达调控。胶质瘤是成人中最常见的脑恶性肿瘤,微小RNA的失调参与了胶质瘤的发生过程。在此,我们发现miR-1297在胶质瘤细胞系和临床胶质瘤组织中的表达均显著降低。通过MTT法、软琼脂集落形成试验和异种移植瘤形成试验,我们表明miR-1297是胶质瘤中的一种肿瘤抑制性微小RNA。我们证明高迁移率族蛋白A1(HMGA1)是胶质瘤细胞中miR-1297的功能靶点。HMGA1在体外和体内均显著促进胶质瘤细胞的生长。总之,我们揭示了胶质瘤中的一种新分子机制,这可能为理解这种脑恶性肿瘤提供新的线索。

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