MicroRNA-940 Inhibits Epithelial-mesenchymal Transition of Glioma Cells Via Targeting ZEB2
Overview
Affiliations
MicroRNAs have been found ectopically expressed in many cancers and play essential roles in tumor EMT progress. Recent studies identified decreased miR-940 expression in glioma cells and may serve as a tumor-suppressor. However, whether miR-940 involve in glioma EMT remain poorly understood. Here we confirmed that miR-940 was significantly reduced in glioma cells and tissues. Introduction of miR-940 dramatically suppressed invasion and migration of glioma cells. Gain-of-function experiments showed ZEB2 as a direct target of miR-940, knockdown of ZEB2 evidently repressed invasive capacity of glioma cells through EMT. Moreover, reintroduction of ZEB2 effectively reversed the tumor suppressive effect of miR-940 treatment. In vivo study showed reduced tumor cell motion in miR-940-injected groups. Spearman's correlation analysis indicated inversely correlated expression of ZEB2 and miR-940 in gliomas and NBTs. Altogether, miR-940-ZEB2 cascade may play important roles in glioma cells invasion and EMT progression, and might provide new therapeutic approaches for better outcomes of GBM patients.
Zhang X, Fang F, Zhang J, Zhang S, Li H, Li B Appl Biochem Biotechnol. 2024; 197(1):497-517.
PMID: 39172343 DOI: 10.1007/s12010-024-05028-9.
A multi-omics approach for biomarker discovery in neuroblastoma: a network-based framework.
Hussein R, Abou-Shanab A, Badr E NPJ Syst Biol Appl. 2024; 10(1):52.
PMID: 38760476 PMC: 11101461. DOI: 10.1038/s41540-024-00371-3.
Xu C, Hou P, Li X, Xiao M, Zhang Z, Li Z Cancer Biol Med. 2024; 21(5).
PMID: 38712813 PMC: 11131044. DOI: 10.20892/j.issn.2095-3941.2023.0510.
miR-940 modulates CD47 to suppress biological functions of lung adenocarcinoma cells.
Long S, Long X, Guo J, Fu L, Huang X, Liu H Am J Cancer Res. 2024; 14(3):1157-1173.
PMID: 38590419 PMC: 10998766. DOI: 10.62347/YYJN3674.
Mo H, Shen J, Zhong Y, Chen Z, Wu T, Lv Y Oncol Res. 2023; 30(4):187-199.
PMID: 37304410 PMC: 10208074. DOI: 10.32604/or.2022.027534.