miR-219-5p targets TBXT and inhibits breast cancer cell EMT and cell migration and invasion

被引:11
|
作者
Ye, Qin [1 ]
Wang, Xing [1 ]
Yuan, Mei [1 ]
Cui, Shuaishuai [2 ]
Chen, Yuanyuan [2 ]
Hu, Zhaodi [1 ]
Liu, Dandan [1 ]
Han, Conghui [3 ]
Li, Bibo [4 ]
Chen, Dahu [2 ]
机构
[1] Jiangsu Normal Univ, Sch Life Sci, Xuzhou 221116, Jiangsu, Peoples R China
[2] Shandong Univ Technol, Sch Life Sci, Zibo 225000, Peoples R China
[3] Xuzhou Cent Hosp, Dept Urol, Xuzhou 221009, Jiangsu, Peoples R China
[4] Nanjing Univ Chinese Med, Dept Urol, Taizhou Hosp, Taizhou 225300, Peoples R China
基金
中国国家自然科学基金;
关键词
EPITHELIAL-MESENCHYMAL TRANSITION; T-BOX GENES; BRACHYURY; MICRORNA; METASTASIS; EXPRESSION; ZEB1;
D O I
10.1042/BSR20210318
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
miR-219-5p has been reported to act as either a tumor suppressor or a tumor promoter in different cancers by targeting different genes. In the present study, we demonstrated that miR-219-5p negatively regulated the expression of TBXT, a known epithelial-mesenchymal transition (EMT) inducer, by directly binding to TBXT 3'-untranslated region. As a result of its inhibition on TBXT expression, miR-219-5p suppressed EMT and cell migration and invasion in breast cancer cells. The re-introduction of TBXT in miR-219-5p overexpressing cells decreased the inhibitory effects of miR-219 on EMT and cell migration and invasion. Moreover, miR-219-5p decreased breast cancer stem cell (CSC) marker genes expression and reduced the mammosphere forming capability of cells. Overall, our study highlighted that TBXT is a novel target of miR-219-5p. By suppressing TBXT, miR-219-5p plays an important role in EMT and cell migration and invasion of breast cancer cells.
引用
收藏
页数:11
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