Abstract

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.

Details

Title
Transcriptional induction of NF-κB-inducing kinase by E2F4/5 facilitates collective invasion of GBM cells
Author
Pflug, Kathryn M. 1 ; Lee, Dong W. 1 ; McFadden, Kassandra 2 ; Herrera, Linda 3 ; Sitcheran, Raquel 1 

 Texas A&M University Health Science Center, Department of Cell Biology and Genetics, School of Medicine, Bryan, USA (GRID:grid.412408.b) 
 Texas A&M University Health Science Center, Department of Cell Biology and Genetics, School of Medicine, Bryan, USA (GRID:grid.412408.b); San Antonio Air Force Base, 59Th Medical Wing, San Antonio, USA (GRID:grid.476822.d) (ISNI:0000 0004 6040 4031) 
 Texas A&M University Health Science Center, Department of Cell Biology and Genetics, School of Medicine, Bryan, USA (GRID:grid.412408.b); Massachusetts General Hospital, Boston, USA (GRID:grid.32224.35) (ISNI:0000 0004 0386 9924) 
Pages
13093
Publication year
2023
Publication date
2023
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2849187739
Copyright
© The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.