Department of Cell Biology and Genetics, School of Medicine, Texas A&M University Health Science Center, Bryan, TX, 77807, USA.
59Th Medical Wing, San Antonio Air Force Base, San Antonio, TX, 78236, USA.
Sci Rep. 2023 Aug 11;13(1):13093. doi: 10.1038/s41598-023-38996-9.
The prognosis of high-grade gliomas, such as glioblastoma multiforme (GBM), is extremely poor due to the highly invasive nature of these aggressive cancers. Previous work has demonstrated that TNF-weak like factor (TWEAK) induction of the noncanonical NF-κB pathway promotes the invasiveness of GBM cells in an NF-κB-inducing kinase (NIK)-dependent manner. While NIK activity is predominantly regulated at the posttranslational level, we show here that NIK (MAP3K14) is upregulated at the transcriptional level in invading cell populations, with the highest NIK expression observed in the most invasive cells. GBM cells with high induction of NIK gene expression demonstrate characteristics of collective invasion, facilitating invasion of neighboring cells. Furthermore, we demonstrate that the E2F transcription factors E2F4 and E2F5 directly regulate NIK transcription and are required to promote GBM cell invasion in response to TWEAK. Overall, our findings demonstrate that transcriptional induction of NIK facilitates collective cell migration and invasion, thereby promoting GBM pathogenesis.
高级别神经胶质瘤(如多形性胶质母细胞瘤,GBM)的预后极差,因为这些侵袭性癌症具有高度侵袭性。先前的研究表明,TNF-weak like factor(TWEAK)诱导非经典 NF-κB 途径会促进 GBM 细胞的侵袭性,这是一种 NF-κB 诱导激酶(NIK)依赖性方式。虽然 NIK 活性主要在翻译后水平受到调节,但我们在这里表明,在侵袭性细胞群体中,NIK(MAP3K14)在转录水平上被上调,在最具侵袭性的细胞中观察到最高的 NIK 表达。NIK 基因表达诱导较高的 GBM 细胞表现出集体侵袭的特征,有助于邻近细胞的侵袭。此外,我们证明 E2F 转录因子 E2F4 和 E2F5 直接调节 NIK 转录,并在 TWEAK 刺激下促进 GBM 细胞侵袭。总的来说,我们的研究结果表明,NIK 的转录诱导促进了细胞的集体迁移和侵袭,从而促进了 GBM 的发病机制。