Department of Neurosurgery, The First Affiliated Hospital of China Medical University, Shenyang, Liaoning, 110001, People's Republic of China.
Department of Tumor Biotherapy and Cancer Research, The First Affiliated Hospital of China Medical University, Shenyang, Liaoning, 110001, People's Republic of China.
Cell Mol Neurobiol. 2022 Oct;42(7):2321-2335. doi: 10.1007/s10571-021-01107-1. Epub 2021 May 28.
Glioblastomas (GBMs) are the most frequent primary malignancies in the central nervous system. Aberrant activation of WNT/β-catenin signaling pathways is critical for GBM malignancy. However, the regulation of WNT/β-catenin signaling cascades remains unclear. Presently, we observed the increased expression of ZEB2 and the decreased expression of miR-637 in GBM. The expression of miR-637 was negatively correlated with ZEB2 expression. miR-637 overexpression overcame the ZEB2-enhanced cell proliferation and G1/S phase transition. Besides, miR-637 suppressed the canonical WNT/β-catenin pathways by targeting WNT7A directly. Gain- and loss-of-function experiments with U251 mice demonstrated that miR-637 inhibited cell proliferation and arrested the G1/S phase transition, leading to tumor growth suppression. The collective findings suggest that ZEB2 and WNT/β-catenin cascades merge at miR-637, and the ectopic expression of miR-637 disturbs ZEB2/WNT/β-catenin-mediated GBM growth. The findings provide new clues for improving β-catenin-targeted therapy against GBM.
胶质母细胞瘤(GBM)是中枢神经系统中最常见的原发性恶性肿瘤。WNT/β-catenin 信号通路的异常激活对 GBM 的恶性转化至关重要。然而,WNT/β-catenin 信号级联的调节仍不清楚。目前,我们观察到 GBM 中 ZEB2 的表达增加和 miR-637 的表达减少。miR-637 的表达与 ZEB2 表达呈负相关。miR-637 的过表达克服了 ZEB2 增强的细胞增殖和 G1/S 期转变。此外,miR-637 通过直接靶向 WNT7A 抑制经典的 WNT/β-catenin 途径。使用 U251 小鼠的增益和缺失功能实验表明,miR-637 抑制细胞增殖并阻止 G1/S 期转变,从而抑制肿瘤生长。综上所述,ZEB2 和 WNT/β-catenin 级联在 miR-637 处融合,miR-637 的异位表达扰乱了 ZEB2/WNT/β-catenin 介导的 GBM 生长。这些发现为改善针对 GBM 的β-catenin 靶向治疗提供了新的线索。