Effect of silencing mir-373 on proliferation and apoptosis of laryngeal cancer cells and its mechanism
10.16066/j.1672-7002.2024.06.002
- VernacularTitle:沉默miR-373对喉癌细胞增殖、凋亡能力的影响及作用机制研究
- Author:
Lina PENG
1
;
Chuanjun WU
;
Zhaoxu YAO
;
Qian ZHAO
;
Haiping HAN
Author Information
1. 邯郸市中心医院耳鼻喉头颈外二科,河北 邯郸 056001
- Keywords:
Laryngeal Neoplasms;
Cell Proliferation;
Apoptosis;
microrna-373
- From:
Chinese Archives of Otolaryngology-Head and Neck Surgery
2024;31(6):346-350
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE To explore the effect of silencing RNA-373(mir-373)on the proliferation and apoptosis of laryngeal cancer cells and its mechanism.METHODS Laryngeal cancer cells were divided into control group,overexpression group and silence group.Stable overexpression group and silence group were established by cell transfection.MTT assay was used to detect cell proliferation,TUNEL method was used to detect the apoptotic ability,cell invasion was detected by Transwell chamber,cell migration was detected by cell scratch test,Western blot was used to detect the expression of β-Catenin,c-myc,CyclinD1,MMP-9,bc1-2 and Bax in Wnt/β-catenin signaling pathway.RESULTS Compared with over expression group,the expression of mir-373 in silence group was significantly decreased(t=15.062,P<0.05).Compared with the overexpression group,the apoptosis rate was higher and the proliferation rate was lower in the silencing group at different time points(t=31.025,16.453,22.475,29.672,P<0.05).Compared with overexpression group,the invasion ability and migration number of cells in silencing group were lower(t=35.254,37.205,P<0.05).Compared with overexpression group,the expression levels of β-Catenin,c-myc,CyclinD1,MMP-9,bc1-2 protein in silencing group were lower,and Bax protein was higher(t=4.218,5.307,4.609,5.005,4.328,3.984,P<0.05).CONCLUSION Silencing mir-373 may promote apoptosis and inhibit invasion,proliferation and migration of laryngeal cancer cells by promoting Bax expression,inhibiting the expression of β-Catenin,c-myc,CyclinD1,MMP-9 and bc1-2,and blocking Wnt/β-catenin signaling pathway.
