Journal
NEOPLASMA
Volume 66, Issue 3, Pages 350-356Publisher
AEPRESS SRO
DOI: 10.4149/neo_2018_180714N484
Keywords
miR-375; Wnt5a; proliferation; invasion; glioblastoma
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Funding
- Hai Yan Project of Harbin Medical University Cancer Hospital [JJQN2017-01]
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The aberrant expression of microRNA-375 (miR-375) has been proven to be associated with carcinogenesis. However, the role of miR-375 in glioblastoma (GBM) remains unknown. The aim of this study was to investigate miR-375 biological functions and its molecular mechanisms in GBM cells. In this study, real-time PCR results showed that the level of miR-375 expression in GBM tissues and GBM cell lines (U87 and U251) was decreased. Using MTT assay, trans-well migration and invasion assay, we demonstrated that miR-375 overexpression significantly suppress cell proliferation, cell migration and cell invasion capacity in U87 and U251 cells. However, downregulation of miR-375 had reverse effects on cell proliferation, migration and invasion. In association analysis, dual luciferase assay, RT-PCR and western blot analysis results confirmed that miR-375 could target the 3'UTR of Wnt5a mRNA and regulate its protein expression. Further studies also showed that Wnt5a overexpression significantly reversed miR-375-mediated proliferation, migration and invasion in U87 and U251 cells. Therefore, we concluded that miR-375 inhibits proliferation and invasion of GBM by regulating Wnt5a and therefore might be a possible therapeutic agent for GBM.
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