Abstract |
MicroRNAs are involved in the regulation of tumor formation. A previous study suggested that miR-10a promotes glioma cell migration and invasion. However, the effect of miR-10a on the proliferation of glioma cells remains unknown. In this study, we demonstrated that miR-10a promoted proliferation and reduced apoptosis in glioma cells by directly targeting the 3'-UTR of myotubularin-related protein 3 (MTMR3). miR-10a enhanced, while MTMR3 weakened, the growth of glioma in vivo. Ectopic expression of MTMR3 neutralized the effect of miR-10a on glioma. Furthermore, miR-10a and MTMR3 regulated β- catenin expression and genes downstream of the Wnt/β- catenin signaling pathway, such as Bcl-2, c-myc, p-c-Jun, and cleaved caspase-3, to affect the proliferation ability and apoptosis of glioma cells. In conclusion, our results indicated that miR-10a regulated cell proliferation and apoptosis by directly targeting MTMR3 and could function as a prognostic factor for progression of glioma.
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Authors | Yan Yan, Hua Yan, Qin Wang, Le Zhang, Ying Liu, Haimiao Yu |
Journal | The FEBS journal
(FEBS J)
Vol. 286
Issue 13
Pg. 2577-2592
(07 2019)
ISSN: 1742-4658 [Electronic] England |
PMID | 30927504
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2019 Federation of European Biochemical Societies. |
Chemical References |
- MIRN10 microRNA, human
- MicroRNAs
- beta Catenin
- MTMR3 protein, human
- Protein Tyrosine Phosphatases, Non-Receptor
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Topics |
- Adult
- Aged
- Apoptosis
- Brain Neoplasms
(genetics, metabolism, pathology)
- Carcinogenesis
(genetics, metabolism)
- Cell Line, Tumor
- Cell Proliferation
- Female
- Gene Expression Regulation, Neoplastic
- Glioma
(genetics, metabolism, pathology)
- Humans
- Male
- MicroRNAs
(genetics, metabolism)
- Middle Aged
- Protein Tyrosine Phosphatases, Non-Receptor
(genetics, metabolism)
- Wnt Signaling Pathway
- beta Catenin
(genetics, metabolism)
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