Abstract |
Hepatocellular carcinoma (HCC) is one of the leading causes of cancer-related deaths worldwide. Increasing evidence suggests that microRNAs ( miRNAs) are associated with HCC tumorigenesis. The present study was designed to define the role of miR-141 in HCC. The expression of miR-141 was significantly decreased in four HCC cell lines. Overexpression of miR-141 suppressed both the growth and the motility of HCC cells. Furthermore, we identified zinc finger E-box binding homeobox 2 (ZEB2) as a target of miR-141 and miR-141 functioned as a tumor suppressor via ZEB2 targeting in HCC. These data provide a novel potential therapeutic target for HCC treatment.
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Authors | Shi-Min Wu, Hong-Wu Ai, Ding-Yu Zhang, Xiao-Qun Han, Qin Pan, Feng-Ling Luo, Xiao-Lian Zhang |
Journal | Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine
(Tumour Biol)
Vol. 35
Issue 10
Pg. 9993-7
(Oct 2014)
ISSN: 1423-0380 [Electronic] Netherlands |
PMID | 25008569
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Homeodomain Proteins
- MIRN141 microRNA, human
- MicroRNAs
- Repressor Proteins
- ZEB2 protein, human
- Zinc Finger E-box Binding Homeobox 2
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Topics |
- Blotting, Western
- Carcinoma, Hepatocellular
(genetics, metabolism, pathology)
- Cell Line, Tumor
- Disease Progression
- Gene Expression Regulation, Neoplastic
(physiology)
- Genes, Tumor Suppressor
- Homeodomain Proteins
(biosynthesis, genetics)
- Humans
- Liver Neoplasms
(genetics, metabolism, pathology)
- MicroRNAs
(genetics, metabolism)
- Repressor Proteins
(biosynthesis, genetics)
- Reverse Transcriptase Polymerase Chain Reaction
- Zinc Finger E-box Binding Homeobox 2
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