Downregulation of microRNA-214 and overexpression of FGFR-1 contribute to hepatocellular carcinoma metastasis

被引:78
|
作者
Wang, Jian [1 ]
Li, Jingwu [2 ,3 ]
Wang, Xiuchao [1 ]
Zheng, Chen [1 ]
Ma, Weidong [1 ]
机构
[1] Tianjin Med Univ, Tianjin Canc Inst & Hosp, 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
基金
中国国家自然科学基金;
关键词
Hepatocellular carcinoma; miR-214; FGFR-1; Metastasis; FIBROBLAST-GROWTH-FACTOR; TARGET RECOGNITION; CANCER; EXPRESSION; PROLIFERATION;
D O I
10.1016/j.bbrc.2013.08.032
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-214 is one of the most significantly downregulated microRNAs (miRNAs) in hepatocellular carcinoma (HCC). Fibroblast growth factor receptor 1 (FGFR-1) is a miR-214 target gene implicated in the progression of HCC. However, the roles of miR-214 and FGFR-1 in HCC are not fully understood. Here, we analyzed the expression of miR-214 and FGFR-1 in 65 cases of HCC and paired non-neoplastic tissue specimens using real-time PCR and Western blot (WB), respectively. Our data indicated that miR-214 was downregulated and FGFR-1 was overexpressed in HCC compared to the paired non-neoplastic tissues. The low miR-214 expression was correlated with portal vein invasion (p = 0.016) and early recurrence (p = 0.045) in HCC patients. Moreover, the low miR-214 expression was correlated with high positive rate of FGFR-1 in HCC cases (p = 0.020). Our data further demonstrated that miR-214 overexpression in SK-HEP1 and HepG2 cells downregulated FGFR-1 expression and inhibited liver cancer cell invasion. The Luciferase assay results further demonstrated the targeted regulation of FGFR-1 by miR-214. In conclusion, our data indicate that the downregulation of miR-214 in HCC and the upregulation of its target gene FGFR-1 is associated with HCC progression. Therefore, miR-214 and FGFR-1 are potential prognostic markers and therapeutic targets in HCC. (c) 2013 Elsevier Inc. All rights reserved.
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页码:47 / 53
页数:7
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