Dong Huixiao, Hao Xiuzhen, Cui Benliang, Guo Meiling
Jining First People's Hospital, Jining, Shandong, China.
Cell Biochem Funct. 2017 Jul;35(5):260-268. doi: 10.1002/cbf.3271.
Accumulating evidence has shown that miR-429 plays an important role in the development and progression of tumour. However, the role of miR-429 in glioblastoma multiforme (GBM) remains largely unknown. The present study is designed to investigate the function of miR-429 in GBM and to explore the molecular mechanism underlying its function. The expression level of miR-429 was detected in GBM tissues and cell lines by quantitative real-time polymerase chain reaction. The effect of overexpression of miR-429 on in vitro cell proliferation, apoptosis and invasion was examined. Western blot analysis was used to detect the influence of miR-429 on the expression of target gene, and Pearson analysis was used to calculate the correlation between the expression of targets gene and the miR-429 in GBM tissues. Our study shows that miR-429 is downregulated in GBM tissues compared with noncancerous tissues (P < .01). In addition, the expression of miR-429 in GBM cell lines is also significantly lower (P < .01). Enforced expression of miR-429 inhibits GBM cells proliferation, induces apoptosis and suppresses invasion and leads to the downregulation of the SOX2 protein. Moreover, the expression level of miR-429 in GBM tissues shows inverse relationship with the expression level of SOX2 protein. Our findings suggest that miR-429 represents a potential tumour-suppressive miRNA and plays an important role in GBM progression by directly targeting SOX2.
越来越多的证据表明,miR-429在肿瘤的发生发展过程中发挥着重要作用。然而,miR-429在多形性胶质母细胞瘤(GBM)中的作用仍不清楚。本研究旨在探讨miR-429在GBM中的功能,并探索其作用的分子机制。通过定量实时聚合酶链反应检测GBM组织和细胞系中miR-429的表达水平。检测miR-429过表达对体外细胞增殖、凋亡和侵袭的影响。采用蛋白质免疫印迹分析检测miR-429对靶基因表达的影响,并用Pearson分析计算GBM组织中靶基因表达与miR-429之间的相关性。我们的研究表明,与非癌组织相比,GBM组织中miR-429表达下调(P<0.01)。此外,miR-429在GBM细胞系中的表达也显著降低(P<0.01)。miR-429的过表达抑制GBM细胞增殖,诱导凋亡,抑制侵袭,并导致SOX2蛋白表达下调。此外,GBM组织中miR-429的表达水平与SOX2蛋白的表达水平呈负相关。我们的研究结果表明,miR-429是一种潜在的肿瘤抑制性miRNA,通过直接靶向SOX2在GBM进展中发挥重要作用。