Wnt/β-catenin signaling inhibits FBXW7 expression by upregulation of microRNA-770 in hepatocellular carcinoma

被引:23
|
作者
Wu, Wen-Jie [1 ]
Shi, Jia [1 ]
Hu, Gang [2 ]
Yu, Xin [2 ]
Lu, Han [3 ]
Yang, Ming-Liang [4 ]
Liu, Bin [2 ]
Wu, Zhi-Xiang [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Xin Hua Hosp, Dept Pediat Surg, 1665 Kongjiang Rd, Shanghai 200092, Peoples R China
[2] Hubei Polytech Univ, Coll Med, Key Lab Kidney Dis Pathogenesis & Intervent Hubei, Huangshi 435003, Hubei, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Anesthesiol, 197 Rui Jin Er Rd, Shanghai 200025, Peoples R China
[4] Jianli Second Peoples Hosp, Dept Anesthesiol, Jianli 433325, Hubei, Peoples R China
关键词
Hepatocellular carcinoma (HCC); FBXW7; MicroRNA-770; Wnt/beta catenin; TUMOR-SUPPRESSOR GENE; UBIQUITIN LIGASE; CYCLIN-E; F-BOX; CANCER; FBW7; DEGRADATION; MYC;
D O I
10.1007/s13277-015-4452-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
FBXW7 (F-box and WD repeat domain-containing 7) is the F-box protein component of a Skp1-Cul1-F-box protein-type (SCF-type) ubiquitin ligase. Previous studies have shown that FBXW7 serves as a tumor suppressor and is frequently downregulated in many types of human neoplasms. However, the molecular mechanisms for its downregulation remain poorly understood. Hyperactivation of Wnt/beta-catenin signaling pathway is viewed as crucial for tumorigenesis, including hepatocellular carcinoma (HCC). In the present study, we show that protein levels, but not message RNA, of FBXW7 were suppressed by Wnt3a treatment or transfection of a constitutively activated beta-catenin in HCC cells. Besides, microRNA-770 was identified as an important downstream target of Wnt/beta-catenin signaling, to inhibit FBXW7 expression through targeting its 3'-untranslated region. Thus, our results suggest a previously unknown Wnt/beta-catenin-miR-770-FBXW7 molecular network in the HCC development.
引用
收藏
页码:6045 / 6051
页数:7
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