MicroRNA-182 downregulates metastasis suppressor 1 and contributes to metastasis of hepatocellular carcinoma

被引:139
|
作者
Wang, Jian [1 ]
Li, Jingwu [2 ,3 ]
Shen, Junling [4 ]
Wang, Chen [1 ]
Yang, Lili [1 ]
Zhang, Xinwei [1 ]
机构
[1] Tianjin Med Univ, Canc Hosp & Inst, Dept Abdominal Oncol 4, Tianjin 300060, Peoples R China
[2] Tangshan Peoples Hosp, Dept Abdominal Oncol, Tangshan 063001, Peoples R China
[3] Hebei Med Univ, Shijiazhuang 050017, Peoples R China
[4] Qingdao Agr Univ, Qingdao 266109, Peoples R China
来源
BMC CANCER | 2012年 / 12卷
基金
中国国家自然科学基金;
关键词
Hepatocellular carcinoma; miR-182; Metastasis suppressor 1; Metastasis; TARGET RECOGNITION; BLADDER-CANCER; MIM-B; EXPRESSION; PROTEIN; ACTIN; RECURRENCE; REPRESSION; RESECTION; MTSS1;
D O I
10.1186/1471-2407-12-227
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: miR-182 is one of the most significantly up-regulated miRNAs in hepatocellular carcinoma (HCC). Metastasis suppressor 1 (MTSS1), one target gene of miR-182, plays an important role in the metastasis of cancers. However, it remains unclear what role does function and mechanism of miR-182 and MTSS1play in HCC. Methods: miR-182 expression was tested in 86 cases of paired HCC and normal tissues by real-time PCR and the relationships between miR-182 expression and clinicopathological parameters were analyzed. The expression of MTSS1 was evaluated by immunohistochemistry and western blot in the above tissues and its correlation with miR-182 expression was analyzed. Moreover, western blot and invasion assays were performed after transfection of pre-miR-182 or anti-miR-182 to HCC cell lines. In addition, luciferase assays was performed to confirm the regulation of miR-182 on MTSS1. Results: Compared with normal tissue, miR-182 was up-regulated and MTSS1 was down-regulated in HCC tissues. Moreover, the over-expression of miR-182 was correlated with intrahepatic metastasis (p = 0.034) and poor prognosis (p = 0.039) of HCC patients. There was a negative correlation between miR-182 and MTSS1 expression in both HCC tissues (r = -0.673, p < 0.01) and HCC cell lines (r = -0.931, p = 0.021). Furthermore, the up-regulation of miR-182 resulted in the down-regulation of MTSS1 and increased invasive potential of HUH-1, and reverse results were also confirmed when the expression of miR-182 was inhibited. In addition, the results of the luciferase assay demonstrated the targeted regulation of miR-182 on MTSS1. Conclusions: miR-182 could promote metastasis of HCC and inhibit the expression of MTSS1. miR-182 and MTSS1 are potential prognostic markers and/or therapeutic targets in HCC.
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页数:10
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