College of Life Sciences, Beijing Normal University, Beijing 100875, China.
National Institute of Biological Sciences, Beijing 102206, China.
Int J Mol Sci. 2022 Jan 20;23(3):1123. doi: 10.3390/ijms23031123.
Glioblastoma is an aggressive cancer of the nervous system that accounts for the majority of brain cancer-related deaths. Through cross-species transcriptome studies, we found that Engrailed 1 (EN1) is highly expressed in serum-free cultured glioma cells as well as glioma tissues, and increased expression level predicts a worse prognosis. EN1 controls glioma cell proliferation, colony formation, migration, and tumorigenic capacity in vivo. It also influences sensitivity of glioma cells to γ-ray irradiation by regulating intracellular ROS levels. Mechanistically, EN1 influences Hedgehog signaling by regulating the level of Gli1 as well as primary cilia length and the primary cilia transport-related protein TULP3. In conclusion, we demonstrate that EN1 acts as an oncogenic regulator that contributes to glioblastoma pathogenesis and could serve as a diagnostic/prognostic marker and therapeutic target for glioblastoma.
胶质母细胞瘤是一种侵袭性的神经系统癌症,占大多数与脑癌相关的死亡病例。通过跨物种转录组研究,我们发现 Engrailed 1(EN1)在无血清培养的神经胶质瘤细胞以及神经胶质瘤组织中高度表达,且表达水平升高预示着预后更差。EN1 控制神经胶质瘤细胞的增殖、集落形成、迁移和体内致瘤能力。它还通过调节细胞内 ROS 水平来影响神经胶质瘤细胞对γ射线照射的敏感性。从机制上讲,EN1 通过调节 Gli1 水平以及初级纤毛长度和与初级纤毛运输相关的蛋白 TULP3 来影响 Hedgehog 信号通路。总之,我们证明 EN1 作为一种致癌调节剂,有助于胶质母细胞瘤的发病机制,可作为胶质母细胞瘤的诊断/预后标志物和治疗靶点。