[No authors listed]
Accumulating evidence suggests that microRNAs (miRNAs) play a key role in the biological behaviors and progression of glioma. However, the function and bioâmolecular mechanisms of miRâ342 in glioma remain largely unclear. In the present study, reverse transcription quantitativeâpolymerase chain reaction and western blotting were performed to determine the mRNA and protein expression levels of the factors investigated. MTT assay was performed to examine the proliferation rates. Luciferase reporter assay was performed to test the binding between miRNAâ342 and its putative target. Data indicated that miRâ342 expression was markedly decreased in human glioma tissues and cell line U87, and reduced miRâ342 expression significantly promoted cell proliferation. In order to explore the mechanisms, Gâprotein coupled receptor family C group 5 member A (GPRC5A) was identified as a target of miRâ342 and depletion of GPRC5A suppressed cell proliferation. Our findings demonstrated that miRâ342 regulates the cell proliferation of glioma by targeting GPRC5A, which indicates that miRâ342 is a target of interest regarding the treatment of refractory glioma, and it may provide a promising prognostic and therapeutic strategy for glioma treatment.
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