MiR-205-3p suppresses bladder cancer progression via GLO1 mediated P38/ERK activation

被引:4
|
作者
Zou, Zhenhai [1 ]
Cheng, Qi [1 ]
Zhang, Shuchao [1 ]
Wang, Zhongqi [1 ]
Song, Xue [1 ,2 ]
Geng, Zhijun [2 ]
Mei, Zhijie [1 ]
Liu, Jianmin [1 ]
Liu, Beibei [1 ]
Guo, Yuanyuan [1 ]
机构
[1] Bengbu Med Coll, Affiliated Hosp 1, Dept Urol, 287 Changhuai Rd, Bengbu 233040, Anhui, Peoples R China
[2] Bengbu Med Coll, Affiliated Hosp 1, Cent Lab, Bengbu 233040, Anhui, Peoples R China
关键词
Bladder cancer; MiR-205-3p; GLO1; P38/ERK; MAPK PATHWAY; PROLIFERATION; EXPRESSION; TARGETS;
D O I
10.1186/s12885-023-11175-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs) have been reported to serve as potential biomarkers in bladder cancer and play important roles in cancer progression. This study aimed to investigate the biological role of miR-205-3p in bladder cancer. We showed that miR-205-3p was significantly down-regulated in bladder cancer tissues and cells. Moreover, overexpression of miR-205-3p inhibited bladder cancer progression in vitro. Then we confirmed that GLO1, a downstream target of miR-205-3p, mediated the effect of miR-205-3p on bladder cancer cells. In addition, we found that miR-205-3p inhibits P38/ERK activation through repressing GLO1. Eventually, we confirmed that miR-205-3p inhibits the occurrence and progress of bladder cancer by targeting GLO1 in vivo by nude mouse tumorigenesis and immunohistochemistry. In a word, miR-205-3p inhibits proliferation and metastasis of bladder cancer cells by activating the GLO1 mediated P38/ERK signaling pathway and that may be a potential therapeutic target for bladder cancer.
引用
收藏
页数:13
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