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RETRACTED: MicroRNA-124 inhibits cell proliferation, invasion and migration by targeting CAV1 in bladder cancer (Retracted article. See vol. 23, 2022)
被引:28
|作者:
Zhou, Wandan
[1
]
He, Leye
[2
]
Dai, Yinbo
[2
]
Zhang, Yichuan
[2
]
Wang, Jinrong
[2
]
Liu, Bin
[2
]
机构:
[1] Cent South Univ, Xiangya Hosp 2, Urol Grp, Dept Operat Ctr, Changsha 410011, Hunan, Peoples R China
[2] Cent South Univ, Xiangya Hosp 3, Dept Urol, 138 Tongzipo Rd, Changsha 410013, Hunan, Peoples R China
关键词:
bladder cancer;
microRNA;
caveolin;
1;
tumour suppressor;
CAVEOLIN-1;
MIR-124;
EXPRESSION;
CARCINOMA;
METHYLATION;
APOPTOSIS;
GENES;
GRADE;
D O I:
10.3892/etm.2018.6537
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
MicroRNAs (miRs) may have promotive or suppressive roles in various human cancers types, but the molecular mechanisms underlying the role of miR-124 in bladder cancer (BC) progression have remained largely elusive. In the present study, it was observed that miR-124 was significantly downregulated in BC tissues compared with that in adjacent non-neoplastic tissues. Furthermore, its expression was also reduced in several human BC cell lines (T24, HT-1376 and 5637) compared with that in the normal bladder epithelial SV-HUC-1 cell line. A low expression of miR-124 in BC patients was significantly associated with advanced malignancy and a poor prognosis. Caveolin 1 (CAV1) was identified as a novel target gene of miR-124, and the expression of CAV1 was negatively regulated by miR-124 in T24 cells. Furthermore, CAV1 was identified to be significantly upregulated in BC tissues and cell lines, and a negative correlation was observed between the expression of miR-124 and CAV1 in BC tissues. Furthermore, restoration of miR-124 expression significantly inhibited the proliferation, migration and invasion of T24 cells, and these effects were impaired following overexpression of CAV1. Taken together, the present results demonstrate that miR-124 has a suppressive role in the proliferation, migration and invasion of BC cells by targeting CAV1, which suggests that miR-124 is a potential therapeutic candidate for BC.
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页码:2811 / 2820
页数:10
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