Jin Zheng, Piao Lianhua, Sun Guangchao, Lv Chuanxiang, Jing Yi, Jin Rihua
Department of Neurosurgery, The First Hospital of Jilin University, Changchun 130021, People's Republic of China.
Department of Physiology, College of Basic Medical Sciences, Jilin University, Changchun 130021, People's Republic of China.
Onco Targets Ther. 2020 Feb 4;13:1073-1086. doi: 10.2147/OTT.S232848. eCollection 2020.
Glioma is the most commonly diagnosed primary brain tumor. Dysregulation of long non-coding RNA (lncRNA) is associated with initiation and development of various cancer types including glioma.
The relative expression of lncRNA was analyzed by real time-quantitative polymerase chain reaction (RT-qPCR). Cell counting kit (CCK-8) and flow cytometry analysis were applied to explore the role of prostate androgen-regulated transcript 1 (PART1) in glioma cell lines. Luciferase reporter assay, Western blotting and RT-qPCR were used to investigate the association between PART1, miR-190a-3p and phosphatase and tensin homolog deleted on chromosome ten (PTEN) in glioma cell lines.
In the present study, we elucidated a pivotal role and molecular mechanism of lncRNA PART1 in glioma cell lines. It was found that PART1 was significantly downregulated in glioma tissues compared to normal tissues according to TCGA data and our RT-qPCR results. The cell-based assays showed that PART1 suppressed cell proliferation and triggered cell apoptosis in glioma cell lines. PART1 inactivated PI3K/AKT cascade in glioma cell lines. Transfection of constitutively activated AKT (Myr-AKT) reversed PART1 induced cell apoptosis and cell growth arrest. The bioinformatic analysis suggested that miR-190a-3p might bind to PART1. In the dual luciferase reporter assay, we validated that PART1 directly bound to miR-190a-3p in glioma cell lines. Furthermore, there was a reciprocal repression between PART1 and miR-190-3p. In addition, PART1 upregulated PTEN and inactivated PI3K/AKT pathway in glioma cell lines. Moreover, silencing of PTEN reversed PART1 overexpression induced cell growth arrest and apoptosis. In glioma tissues, the Pearson Correlation analysis showed that there was a strong-positive correlation between PART1 level and PTEN mRNA level.
Taken together, the current study revealed a PART1/miR-190a-3p/PTEN/PI3K/AKT axis in glioma and provided novel insights for understanding the complex lncRNA-miRNA network in glioma.
胶质瘤是最常见的原发性脑肿瘤。长链非编码RNA(lncRNA)失调与包括胶质瘤在内的多种癌症类型的发生和发展相关。
通过实时定量聚合酶链反应(RT-qPCR)分析lncRNA的相对表达。应用细胞计数试剂盒(CCK-8)和流式细胞术分析探讨前列腺雄激素调节转录本1(PART1)在胶质瘤细胞系中的作用。采用荧光素酶报告基因检测、蛋白质免疫印迹法和RT-qPCR研究胶质瘤细胞系中PART1、miR-190a-3p与第10号染色体缺失的磷酸酶和张力蛋白同源物(PTEN)之间的关系。
在本研究中,我们阐明了lncRNA PART1在胶质瘤细胞系中的关键作用和分子机制。根据TCGA数据和我们的RT-qPCR结果发现,与正常组织相比,PART1在胶质瘤组织中显著下调。基于细胞的实验表明,PART1抑制胶质瘤细胞系中的细胞增殖并触发细胞凋亡。PART1使胶质瘤细胞系中的PI3K/AKT级联失活。组成型激活的AKT(Myr-AKT)转染逆转了PART1诱导的细胞凋亡和细胞生长停滞。生物信息学分析表明,miR-190a-3p可能与PART1结合。在双荧光素酶报告基因检测中,我们验证了PART1在胶质瘤细胞系中直接与miR-190a-3p结合。此外,PART1与miR-190-3p之间存在相互抑制作用。此外,PART1上调PTEN并使胶质瘤细胞系中的PI3K/AKT通路失活。此外,PTEN沉默逆转了PART1过表达诱导的细胞生长停滞和凋亡。在胶质瘤组织中,Pearson相关性分析表明,PART1水平与PTEN mRNA水平之间存在强正相关。
综上所述,本研究揭示了胶质瘤中的PART1/miR-190a-3p/PTEN/PI3K/AKT轴,并为理解胶质瘤中复杂的lncRNA-miRNA网络提供了新的见解。