Centre for Host-Microbiome Interactions, Faculty of Dentistry, Oral and Craniofacial Sciences, King's College London, London SE1 9RT, UK.
Science for Life Laboratory, KTH-Royal Institute of Technology, SE-17121 Stockholm, Sweden.
Int J Mol Sci. 2024 Jul 18;25(14):7868. doi: 10.3390/ijms25147868.
Glioblastoma (GBM), a highly malignant tumour of the central nervous system, presents with a dire prognosis and low survival rates. The heterogeneous and recurrent nature of GBM renders current treatments relatively ineffective. In our study, we utilized an integrative systems biology approach to uncover the molecular mechanisms driving GBM progression and identify viable therapeutic drug targets for developing more effective GBM treatment strategies. Our integrative analysis revealed an elevated expression of in GBM tumours, designating it as an unfavourable prognostic gene in GBM, as supported by data from two independent GBM cohorts. Further, we pinpointed WZ-4002 as a potential drug candidate to modulate through computational drug repositioning. WZ-4002 directly targeted () and , affecting their dimerization and influencing the activity of adjacent genes, including . We validated our findings by treating U-138 MG cells with WZ-4002, observing a decrease in CHST2 protein levels and a reduction in cell viability. In summary, our research suggests that the WZ-4002 drug candidate may effectively modulate and adjacent genes, offering a promising avenue for developing efficient treatment strategies for GBM patients.
胶质母细胞瘤(GBM)是一种高度恶性的中枢神经系统肿瘤,预后极差,生存率低。GBM 的异质性和复发性使得目前的治疗方法相对无效。在我们的研究中,我们利用综合系统生物学方法来揭示驱动 GBM 进展的分子机制,并确定可行的治疗药物靶点,以开发更有效的 GBM 治疗策略。我们的综合分析显示,在 GBM 肿瘤中表达上调,表明它是 GBM 中不利的预后基因,这得到了两个独立的 GBM 队列数据的支持。此外,我们通过计算药物重定位确定 WZ-4002 是一种潜在的药物候选物,可以调节。WZ-4002 直接靶向()和(),影响它们的二聚化并影响相邻基因的活性,包括。我们通过用 WZ-4002 处理 U-138 MG 细胞来验证我们的发现,观察到 CHST2 蛋白水平下降和细胞活力降低。总之,我们的研究表明,WZ-4002 药物候选物可能有效地调节和相邻基因,为开发有效的 GBM 患者治疗策略提供了有前途的途径。