Pflug Kathryn, Lee Dong, McFadden Kassandra, Herrera Linda, Sitcheran Raquel
Texas A&M Health Science Center.
Res Sq. 2023 Mar 7:rs.3.rs-2622363. doi: 10.21203/rs.3.rs-2622363/v1.
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 increases the invasiveness of glioma 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 ( ) is upregulated at the transcriptional level in invading cell populations, with the highest expression observed in the most invasive cells. Glioma 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 glioma cell invasion in response to TWEAK. Overall, our findings demonstrate that transcriptional induction of NIK facilitates collective cell migration and invasion, thereby promoting glioma pathogenesis.
由于这些侵袭性癌症具有高度侵袭性,多形性胶质母细胞瘤(GBM)等高等级胶质瘤的预后极差。先前的研究表明,肿瘤坏死因子弱样因子(TWEAK)诱导非经典核因子κB(NF-κB)信号通路以核因子κB诱导激酶(NIK)依赖的方式增加胶质瘤细胞的侵袭性。虽然NIK活性主要在翻译后水平受到调控,但我们在此表明,NIK( )在侵袭性细胞群体中在转录水平上调,在侵袭性最强的细胞中表达最高。NIK基因表达高度诱导的胶质瘤细胞表现出集体侵袭的特征,促进邻近细胞的侵袭。此外,我们证明E2F转录因子E2F4和E2F5直接调节NIK转录,并且是响应TWEAK促进胶质瘤细胞侵袭所必需的。总体而言,我们的研究结果表明,NIK的转录诱导促进集体细胞迁移和侵袭,从而促进胶质瘤发病机制。