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Wnt/β-catenin signaling inhibits FBXW7 expression by upregulation of microRNA-770 in hepatocellular carcinoma
- Source :
- Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine. 37(5)
- Publication Year :
- 2015
-
Abstract
- 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/β-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 β-catenin in HCC cells. Besides, microRNA-770 was identified as an important downstream target of Wnt/β-catenin signaling, to inhibit FBXW7 expression through targeting its 3'-untranslated region. Thus, our results suggest a previously unknown Wnt/β catenin-miR-770-FBXW7 molecular network in the HCC development.
- Subjects :
- 0301 basic medicine
Carcinoma, Hepatocellular
F-Box-WD Repeat-Containing Protein 7
Ubiquitin-Protein Ligases
Cell Cycle Proteins
Biology
03 medical and health sciences
0302 clinical medicine
Downregulation and upregulation
Cell Line, Tumor
microRNA
Humans
3' Untranslated Regions
Wnt Signaling Pathway
beta Catenin
Cell Proliferation
F-Box Proteins
Liver Neoplasms
Wnt signaling pathway
LRP6
LRP5
General Medicine
Hep G2 Cells
Ubiquitin ligase
Gene Expression Regulation, Neoplastic
MicroRNAs
030104 developmental biology
030220 oncology & carcinogenesis
Gene Knockdown Techniques
biology.protein
Cancer research
RNA Interference
Signal transduction
WNT3A
Subjects
Details
- ISSN :
- 14230380
- Volume :
- 37
- Issue :
- 5
- Database :
- OpenAIRE
- Journal :
- Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine
- Accession number :
- edsair.doi.dedup.....18b103846d14f938849875e7efc57c9d