MiR-92b inhibits proliferation and invasion of lung cancer by targeting EZH2

Autor: L, Chen, H-Z, Zhuo, J-Y, Wu, L-Y, Lin, Z-L, Huang, J-X, Lu, K-L, Cheng
Rok vydání: 2020
Předmět:
Zdroj: European review for medical and pharmacological sciences. 24(6)
ISSN: 2284-0729
Popis: To verify that miR-92b inhibits proliferation and invasion of lung cancer by targeting EZH2.The expression levels of miR-92b and EZH2 in human bronchial epithelial cell line BEAS-2B and human lung cancer cell line (A549, NCI-H23, NCI-H358, NCI-H1975, PC-9) were detected, and miR-92b mimic, sh-EZH2 expression vector, and plasmid blank vector (blank group) were constructed. Blank group, miR-92b mimic, miR-92b mimic+sh-EZH2 group (combined group) were set up, MTT and transwell were used to detect the proliferation and invasion ability of A549 and NCI-H23 cells, and fluorescein report verified the regulatory relationship of miR-92b to EZH2.The expression level of miR-92b in A549, NCI-H23, NCI-H358, NCI-H1975, and PC-9 cells was lower than that in BEAS-2B cells (p0.05). The expression level of EZH2 was higher than that of BEAS-2B cells (p0.05). A549 and NCI-H23 cells were selected for transfection. After that, the expression level of miR-92 in miR-92b mimic, combined group A549 and NCI-H23 cells was higher than that in blank group (p0.05), and miR-92b mimic had no difference with joint group (p0.05). The expression level of EZH2 in cells of miR-92b mimic, blank group A549, and NCI-H23 was lower than that of combined group (p0.05), and miR-92b mimic was lower than that of blank group (p0.05). After the overexpression of miR-92b, pmirGLO-EZH2-3'UT Wt luciferase activity decreased significantly (p0.05) but had no effect on pmirGLO-EZH2-3'UTR Mut Luciferase activity (p0.05). Cell proliferation ability and invasion ability of A549 cells and NCI-H23 cells in miR-92b mimic group were lower than those in blank group (p0.05), while those in combined group were higher than those in miR-92b mimic group (p0.05).MiR-92b inhibits proliferation and invasion of lung cancer cells through targeted inhibition of EZH2, which is a potential target for future treatment of lung cancer.
Databáze: OpenAIRE