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MicroRNA-15b suppresses the growth and invasion of glioma cells through targeted inhibition of cripto-1 expression.
- Source :
-
Molecular medicine reports [Mol Med Rep] 2016 Jun; Vol. 13 (6), pp. 4897-903. Date of Electronic Publication: 2016 Apr 14. - Publication Year :
- 2016
-
Abstract
- Gliomas are the most common type of malignant brain tumor. Studies have identified that miR‑15b is negatively correlated with cripto-1 expression in glioma cells, and these molecules serve an important role in cancer development and progression. The current study was undertaken to further examine the association between these two molecules. Fluorescent quantitative PCR confirmed that miR‑15b expression was significantly downregulated in glioma tissue while cripto‑1 expression was significantly increased. Subsequent to transfection with miR‑15b mimics, cripto‑1 expression was significantly suppressed, and dual luciferase reporter assays further demonstrated that miR‑15b regulates cripto‑1 in a targeted manner. Furthermore, miR‑15b inhibited proliferation and invasion, and promoted apoptosis of glioma cells while downregulating the expression of MMP‑2 and MMP‑9. In contrast, cripto‑1 expression had the opposite effects. Co‑transfection with miR‑15b mimics and the cripto‑1 overexpression vector overcame the inhibitory action of miR‑15b on cripto‑1. Therefore, it is suggested that miR‑15b modulates cell growth and invasion through targeted regulation of cripto‑1 expression in glioma cells. This observation may provide novel targets for the prevention and treatment of gliomas.
- Subjects :
- 3' Untranslated Regions
Apoptosis
Binding Sites
Brain Neoplasms pathology
Cell Cycle
Cell Line, Tumor
Cell Proliferation
Glioma pathology
Humans
Brain Neoplasms genetics
GPI-Linked Proteins genetics
Gene Expression Regulation, Neoplastic
Glioma genetics
Intercellular Signaling Peptides and Proteins genetics
MicroRNAs genetics
Neoplasm Proteins genetics
RNA Interference
Subjects
Details
- Language :
- English
- ISSN :
- 1791-3004
- Volume :
- 13
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Molecular medicine reports
- Publication Type :
- Academic Journal
- Accession number :
- 27082313
- Full Text :
- https://doi.org/10.3892/mmr.2016.5126