Effect of interference in YAP expression on apoptosis of bladder cancer cells by regulation of Wnt/β-catenin signaling pathway
10.3969/j.issn.1000-4718.2018.02.008
- VernacularTitle:干扰Yes相关蛋白表达调控Wnt/β-catenin信号通路影响膀胱癌细胞凋亡
- Author:
Bang-Jian LIU
1
;
Qi WANG
;
De-Xin YU
;
Ren ZHAO
Author Information
1. 太和县第二人民医院泌尿外科
- Keywords:
Bladder cancer;
Apoptosis;
Yes-associated protein;
Wnt/β-catenin signaling pathway
- From:
Chinese Journal of Pathophysiology
2018;34(2):239-244
- CountryChina
- Language:Chinese
-
Abstract:
AIM:To investigate the effect of interference in Yes-associated protein(YAP)expression on blad-der cancer cell apoptosis and its mechanisms.METHODS:Bladder cancer cell line T-24 was used as the target and divid-ed into control group(no treatment),small interfering RNA negative control(siRNA-NC)group,and YAP siRNA group. The expression levels of YAP at mRNA and protein levels in the transfected cells of each group were detected by real -time PCR and Western blot,respectively.The cell viability was measured by MTT assay.The apoptosis was analyzed by flow cytometry.The protein expression levels of β-catenin and c-Myc were determined by Western blot.The cells in YAP siRNA group were treated with Wnt/β-catenin signaling pathway inhibitor FH 535, and then the cell viability and apoptosis were analyzed by MTT assay and flow cytometry,respectively.RESULTS:The expression of YAP at mRNA and protein levels in YAP siRNA group was significantly lower than that in control group(P<0.05).The cell viability and the expression levels of c-Myc and β-catenin in YAP siRNA group were significantly lower than those in control group(P<0.05),while the apoptotic rate was significantly higher than that in control group(P<0.05).The cell viability in YAP siRNA+FH535 group was decreased significantly,while the apoptotic rate was increased as compared with YAP siRNA group(P<0.05). CONCLUSION:Interfering with the expression of YAP inhibits the viability of bladder cancer cells by inhibiting the Wnt /β-catenin signaling pathway,thus promoting apoptosis of bladder cancer cells.
