基因敲除
下调和上调
糖酵解
癌症研究
转移
胶质母细胞瘤
肿瘤进展
细胞凋亡
生物
信号转导
U87型
细胞生物学
化学
细胞生长
肺
癌基因
细胞培养
肺癌
蛋白质表达
基因表达调控
免疫组织化学
医学
作者
Liang Zhang,Fei Li,Lingxue Zhang,Jiaqi Ma,Bochuan Liu,Yingying Chen,Xiaobing Jiang,Wenwen Gao,Wei Yao,Xue Li,Haikang Zhao,Jun Xu
摘要
Glioblastoma (GBM) is the most common and lethal primary intracranial tumor, and glycolysis has been reported to play a critical role in its progression. Formin-binding protein 1 (FNBP1) has been implicated in GBM progression; however, the precise molecular mechanisms remain unclear. In this study, we demonstrated that FNBP1 expression was significantly higher in GBM tissues compared with adjacent tissues. Elevated FNBP1 expression was correlated with higher tumor grade and reduced 5-year survival in GBM patients. In vitro, knockdown of FNBP1 inhibited proliferation, invasion, and glycolysis, while promoting apoptosis in GBM cells. Mechanistically, RNA-binding motif protein 15B (RBM15B) increased the m6A modification level of FNBP1 mRNA, and insulin-like growth factor 2 mRNA-binding protein 2 (IGF2BP2) recognized this m6A mark and enhanced the stability of FNBP1 mRNA. Furthermore, FNBP1 interacted with LIM and SH3 Domain Protein 1 (LASP1), upregulating LASP1 protein expression and subsequently activating the Smad3 signaling pathway to promote glycolysis. In vivo, subcutaneous xenograft models were established using U251/U87 cells, and a lung metastasis model was generated via tail vein injection of U87 cells. FNBP1 knockdown significantly suppressed tumor growth in the subcutaneous model and reduced the number of lung nodules in the metastasis model. In conclusion, FNBP1, regulated by the RBM15B-m6A-IGF2BP2 axis, promotes GBM progression by interacting with LASP1 to activate Smad3-mediated glycolysis.
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