Journal
SCIENCEASIA
Volume 48, Issue 6, Pages 711-717Publisher
SCIENCE SOCIETY THAILAND
DOI: 10.2306/scienceasia1513-1874.2022.100
Keywords
glioma; MYT1L; migration; invasion; Notch signaling
Categories
Funding
- Open Foundation of Zhejiang Provincial Key Laboratory of Aging and Neurological Disorder Research
Ask authors/readers for more resources
This study reveals that MYT1L gene plays a role in promoting migration and invasion of glioma cells. Through activation of the Notch signaling pathway, MYT1L enhances cell migration and invasion, while inhibition of MYT1L or blocking the Notch pathway suppresses these processes. These findings suggest that MYT1L could be a potential target for glioma treatment.
MYT1L gene has been associated with various brain diseases as it affects many neuronal and biological processes of nerve cells. However, the role of MYT1L in glioma cell migration and invasion and its mechanism of action are still unclear. In this study, MYT1L was successfully silenced in U87 and A172 cells, and overexpressed in U251 cells using lentiviral vectors. The expression levels of MYT1L in glioma cells were assessed by real-time PCR and Western blot analysis. The effect of MYT1L on migration and invasion was examined by a Transwell assay. We found that MYT1L enhanced cell migration and invasion whereas knockdown of MYT1L suppressed migration and invasion in glioma cells. We also demonstrated that MYT1L activated the Notch signaling pathway, and that treatment with the Notch inhibitor DAPT inhibited the migration and invasion of glioma cells. These results suggest that MYT1L may be considered a useful and potential target in the treatment of glioma.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available