MiR-183-5p promotes migration and invasion of prostate cancer by targeting TET1

被引:1
|
作者
Feng, Yuehua [1 ]
Wang, Kai [2 ]
Qin, Minchao [3 ]
Zhuang, Qianfeng [3 ]
Chen, Zhen [3 ]
机构
[1] Soochow Univ, Affiliated Hosp 3, Clin Med Res Ctr, Changzhou, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Sir Run Run Hosp, Dept Urol, Nanjing, Jiangsu, Peoples R China
[3] Soochow Univ, Affiliated Hosp 3, Dept Urol, Changzhou, Jiangsu, Peoples R China
关键词
Prostatic cancer; miR-183-5p; Migration; Invasion; CELL-PROLIFERATION; BREAST-CANCER; PROGRESSION; SUPPRESSES; DEMETHYLATION; MICRORNAS; APOPTOSIS; CLUSTER;
D O I
10.1186/s12894-023-01286-7
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
BackgroundProstate cancer (PCa) is one of the common malignant tumors worldwide. MiR-183-5p has been reported involved in the initiation of human PCa, this study aimed to investigate whether miR-183-5p affects the development of prostate cancer.MethodsIn this study, we analyzed the expression of miR-183-5p in PCa patients and its correlation with clinicopathological parameters based on TCGA data portal. CCK-8, migration assay and invasion and wound-healing assay were performed to detect proliferation, migration and invasion in PCa cells.ResultsWe found the expression of miR-183-5p was significantly increased in PCa tissues, and high expression of miR-183 was positively associated with poor prognosis of PCa patients. Over-expression of miR-183-5p promoted the migration, invasion capacities of PCa cells, whereas knockdown of miR-183-5p showed reversed function. Furthermore, luciferase reporter assay showed TET1 was identified as a direct target of miR-183-5p, which was negatively correlation with miR-183-5p expression level. Importantly, rescue experiments demonstrated TET1 over-expression could reverse miR-183-5p mimic induced-acceleration of PCa malignant progression.ConclusionOur results indicated that miR-183-5p could act as a tumor promoter in PCa and it accelerated the malignant progression of PCa by directly targeting and down-regulating TET1.
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页数:9
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