[No authors listed]
MicroRNAs (miRNAs/miRs) are a class of endogenous and nonâcoding RNAs that are present in eukaryotes. In previous studies, miRNAs have been revealed to have an important role in cell growth and apoptosis. In the present study, the function of a novel and rarely studied miRNA, miRâ4530, was investigated in human umbilical vein endothelial cells (HUVECs). The expression level of miRâ4530 in HUVECs was investigated using reverse transcriptionâquantitative polymerase chain reaction following transfection with miRâ4530 precursor plasmids, antiâmiRâ4530 plasmids and empty vector plasmids. Following this, it was revealed that overexpression of miRâ4530 can suppress cell proliferation and enhance cell apoptosis. TargetScan analysis suggested that Ras p21 protein activator 1 (RASA1) is a target gene of miRâ4530. The results of a dualâluciferase reporter assay also suggested that miRâ4530 targets RASA1. Furthermore, the results of dualâluciferase reporter assay suggested that miRâ4530 enhanced luciferase activity of the wild-type reporter, but not the mutant RASA1 reporter activity, thus suggesting that miRâ4530 enhances the expression of RASA1. In addition, western blot analysis demonstrated that the protein expression level of RASA1 was enhanced following upregulation of miRâ4530. The exact mechanism underlying this process has not yet been determined and requires further investigation. In addition, a RASA1 overexpression plasmid vector was transfected into HUVECs. The results suggest that overexpression of RASA1 suppresses cell growth and promotes apoptosis, which was in agreement with the results regarding the overexpression of miRâ4530. To investigate how miRNAâ4530 affects cellular function, numerous proteins associated with the extracellular signalâregulated kinase (ERK)/mitogenâactivated protein kinase (MAPK) and phosphoinositide 3âkinase (PI3K)/AKT serine/threonine kinase pathways were investigated via western blot analysis. The results suggested that miRNAâ4530 suppresses cell proliferation and enhances apoptosis by targeting RASA1 via the ERK/MAPK and PI3K/AKT signaling pathways.
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