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miRNA-22 suppresses colon cancer cell migration and invasion by inhibiting the expression of T-cell lymphoma invasion and metastasis 1 and matrix metalloproteinases 2 and 9
被引:76
|作者:
Li, Bo
[1
]
Song, Yan
[1
]
Liu, Tong-Jun
[1
]
Cui, You-Bin
[2
]
Jiang, Yang
[1
]
Xie, Zhong-Shi
[1
]
Xie, Shu-Li
[3
]
机构:
[1] Jilin Univ, Affiliated Hosp 3, Dept Colorectal & Anal Surg, Changchun 130033, Jilin, Peoples R China
[2] Jilin Univ, Affiliated Hosp 1, Dept Thorac Surg, Changchun 130033, Jilin, Peoples R China
[3] Jilin Univ, Affiliated Hosp 1, Dept Hepatobiliary Surg, Changchun 130033, Jilin, Peoples R China
关键词:
miRNA-22;
colon cancer;
invasion;
T-cell lymphoma invasion and metastasis 1;
PREDICTS POOR-PROGNOSIS;
TIAM1;
OVEREXPRESSION;
MICRORNA-22;
CARCINOMA;
MIR-22;
ACTIVATION;
D O I:
10.3892/or.2013.2300
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Emerging evidence has demonstrated the altered expression of mRNAs in cancer development and progression. In this study, the precise role of miRNA-22 (miR-22) in colon cancer cells was investigated. Upon transfection with a miR-22 expression vector, the viability of HCT-116 human colon cancer cells was significantly reduced and tumor cell migration and invasion capacity were also suppressed. Computational in silico analysis predicted that T-cell lymphoma invasion and metastasis 1 (TIAM1) is a target gene of miR-22. This was confirmed by qRT-PCR and western blotting, which showed that miR-22 expression inhibited TIAM1 mRNA and protein expression, respectively. In addition, the expression of pro-invasive gene matrix metalloproteinases 2 and 9 (MMP-2 and MMP-9) and pro-angiogenic protein vascular endothelial growth factor (VEGF) were also reduced by miR-22 expression. Collectively, these data suggest that miR-22 may act as a tumor suppressor in colon cancer, most likely by targeting TIAM1 expression.
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页码:1932 / 1938
页数:7
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