The Role of miR-375-3p and miR-200b-3p in Gastrointestinal Stromal Tumors.
Ugne GyvyteRokas LukoseviciusRuta InciuraiteGreta StreleckieneGreta GudoityteJustina BekampyteSerena ValentiniVioleta SaltenienePaulius RuzgysSaulius SatkauskasKristina ZvinieneJuozas KupcinskasJurgita SkiecevicienePublished in: International journal of molecular sciences (2020)
Deregulated microRNA (miRNA) expression profiles and their contribution to carcinogenesis have been observed in virtually all types of human cancer. However, their role in the pathogenesis of rare mesenchymal gastrointestinal stromal tumors (GISTs) is not well defined, yet. In this study, we aimed to investigate the role of two miRNAs strongly downregulated in GIST-miR-375-3p and miR-200b-3p-in the pathogenesis of GIST. To achieve this, miRNA mimics were transfected into GIST-T1 cells and changes in the potential target gene mRNA and protein expression, as well as alterations in cell viability, migration, apoptotic cell counts and direct miRNA-target interaction, were evaluated. Results revealed that overexpression of miR-375-3p downregulated the expression of KIT mRNA and protein by direct binding to KIT 3'UTR, reduced GIST cell viability and migration rates. MiR-200b-3p lowered expression of ETV1 protein, directly targeted and lowered expression of EGFR mRNA and protein, and negatively affected cell migration rates. To conclude, the present study identified that miR-375-3p and miR-200b-3p have a tumor-suppressive role in GIST.
Keyphrases
- binding protein
- poor prognosis
- cell migration
- endothelial cells
- small cell lung cancer
- stem cells
- protein protein
- single cell
- amino acid
- bone marrow
- acute lymphoblastic leukemia
- epidermal growth factor receptor
- papillary thyroid
- dna methylation
- genome wide
- risk assessment
- peripheral blood
- drug delivery
- climate change
- cancer therapy
- induced pluripotent stem cells
- genome wide identification