MiR-381 functions as a tumor suppressor in colorectal cancer by targeting Twist1

被引:53
作者
He, Xinxin [1 ]
Wei, Yangnian [1 ]
Wang, Yong [1 ]
Liu, Ling [1 ]
Wang, Wen [1 ]
Li, Nianfeng [1 ]
机构
[1] Cent South Univ, Xiangya Hosp, Dept Hepatobiliary & Pancreat Surg, 87 Xiangya Rd, Changsha 410008, Hunan, Peoples R China
关键词
colorectal cancer; miR-381; twist family bHLH transcription factor 1; Twist1; epithelial-mesenchymal transition; EMT; MESENCHYMAL TRANSITION; UP-REGULATION; N-CADHERIN; MICRORNAS; TUMORIGENESIS; METASTASIS; INVASION; GROWTH; EXPRESSION; DIAGNOSIS;
D O I
10.2147/OTT.S99228
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
MiR-381 has been reported to be dysregulated in several human cancers. However, the function and mechanism of miR-381 in colorectal cancer (CRC) remains unclear. In the present study, the miR-381 expression was assessed in a cohort of 113 CRC specimens using real-time quantitative polymerase chain reaction (RTq-PCR), which demonstrated that miR-381 was significantly downregulated in CRC and correlated with distant metastasis and tumor, node, and metastasis (TNM) stage. Functional study revealed that restoration of miR-381 significantly inhibited the invasion, migration, and epithelial-mesenchymal transition (EMT) of CRC cells. Luciferase reporter assay validated that Twist1, an important EMT inducer, was a direct target of miR-381, and rescued Twist1 attenuated the function of miR-381 in CRC cells. Correlation analysis also revealed an inverse correlation between miR-381 and Twist1 expression levels in CRC specimens. Taken together, our results highlight the significance of miR-381/Twist1 interaction in the development and progression of CRC, and suggest that restoration of miR-381 may be a potential therapeutic strategy for the patients with CRC.
引用
收藏
页码:1231 / 1239
页数:9
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