Zheng Kebin, Xie Haipeng, Wu Wensong, Wen Xichao, Zeng Zhaomu, Shi Yanfang
Department of Neurosurgery, Affiliated Hospital of Hebei University, No.212Yuhua Road, Lianchi District, Baoding, 071000, Hebei, China.
Cancer Cell Int. 2021 Jan 7;21(1):27. doi: 10.1186/s12935-020-01699-6.
Increasing studies have revealed that circular RNAs (CircRNAs) make great contributions to regulating tumor progression. Therefore, we intended to explore the expression characteristics, function, and related mechanisms of a novel type of circRNA, PIP5K1A, in glioma.
Firstly, reverse transcription-polymerase chain reaction (RT-PCR) was carried out to examine CircPIP5K1A expression in glioma tissues and adjacent normal tissues, and the correlation between CircPIP5K1A level and the clinical-pathological indicators of glioma was analyzed. Then, the CircPIP5K1A expression in various glioma cell lines was detected, and CircPIP5K1A overexpression and knockdown cell models were constructed. Subsequently, cell proliferation and viability were detected by the CCK8 method and BrdU staining. Cell apoptosis was detected by flow cytometry, and cell invasion was examined by Transwell assay. The expression of TCF12, PI3K/AKT pathway apoptotic related proteins (Caspase3, Bax, and Bcl2) and epithelial-mesenchymal transition (EMT) markers (E-cadherin, Vimentin, and N-cadherin) was determined by western blot or RT-PCR.
The results manifested that CircPIP5K1A was upregulated in glioma tissues (compared with that in normal adjacent tissues), and overexpressed CircPIP5K1A was related to glioma volume and histopathological grade. Functionally, overexpressing CircPIP5K1A notably elevated glioma cell proliferation, invasion, and EMT and inhibited apoptosis both in vivo and in vitro. Besides, CircPIP5K1A upregulated TCF12 and PI3K/AKT activation. Bioinformatics analysis testified that miR-515-5p was a common target of CircPIP5K1A and TCF12, while the dual-luciferase reporter assay and RNA immunoprecipitation (RIP) experiment further confirmed that CircPIP5K1A targeted miR-515-5p, which bound the 3'-untranslated region (UTR) of TCF12.
Overall, the study illustrated that CircPIP5K1A is a potential prognostic marker in glioma and regulates glioma evolvement by modulating the miR-515-5p-mediated TCF12/PI3K/AKT axis.
越来越多的研究表明,环状RNA(CircRNAs)在调节肿瘤进展方面发挥着重要作用。因此,我们旨在探讨一种新型环状RNA,即PIP5K1A,在胶质瘤中的表达特征、功能及相关机制。
首先,进行逆转录-聚合酶链反应(RT-PCR)检测CircPIP5K1A在胶质瘤组织和相邻正常组织中的表达,并分析CircPIP5K1A水平与胶质瘤临床病理指标之间的相关性。然后,检测各种胶质瘤细胞系中CircPIP5K1A的表达,并构建CircPIP5K1A过表达和敲低细胞模型。随后,采用CCK8法和BrdU染色检测细胞增殖和活力。通过流式细胞术检测细胞凋亡,采用Transwell实验检测细胞侵袭。通过蛋白质印迹法或RT-PCR检测TCF12、PI3K/AKT通路凋亡相关蛋白(Caspase3、Bax和Bcl2)以及上皮-间质转化(EMT)标志物(E-钙黏蛋白、波形蛋白和N-钙黏蛋白)的表达。
结果表明,CircPIP5K1A在胶质瘤组织中上调(与相邻正常组织相比),且CircPIP5K1A过表达与胶质瘤体积和组织病理学分级相关。在功能上,过表达CircPIP5K1A显著提高了胶质瘤细胞的增殖、侵袭能力以及EMT水平,并在体内和体外均抑制了细胞凋亡。此外,CircPIP5K1A上调了TCF12和PI3K/AKT的激活。生物信息学分析证实miR-515-5p是CircPIP5K1A和TCF12的共同靶点,而双荧光素酶报告基因检测和RNA免疫沉淀(RIP)实验进一步证实CircPIP5K1A靶向miR-515-5p,后者与TCF12的3'-非翻译区(UTR)结合。
总体而言,该研究表明CircPIP5K1A是胶质瘤中一种潜在的预后标志物,并通过调节miR-515-5p介导的TCF12/PI3K/AKT轴来调节胶质瘤的进展。